NOTCH1 Gene Complete Identifier and Functional Mapping Reference
Provide a comprehensive cross-database identifier and functional mapping reference for human NOTCH1. This should serve as a definitive lookup resource …
Provide a comprehensive cross-database identifier and functional mapping reference for human NOTCH1. This should serve as a definitive lookup resource for researchers. ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 1: GENE IDENTIFIERS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Provide ALL gene-level database identifiers: - HGNC ID and approved symbol - Ensembl gene ID (ENSG) - NCBI Entrez Gene ID - OMIM gene/locus ID - Genomic location: chromosome, start position, end position, strand ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 2: TRANSCRIPT IDENTIFIERS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ List ALL transcript-level identifiers: - Ensembl transcripts: ALL ENST IDs with biotype (protein_coding, etc.) How many total transcripts? - RefSeq transcripts: ALL NM_ mRNA accessions Mark which is MANE Select (canonical clinical standard) - CCDS IDs: ALL consensus coding sequence identifiers For the CANONICAL/MANE SELECT transcript: - List ALL exon IDs (ENSE) with genomic coordinates - Total exon count ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 3: PROTEIN IDENTIFIERS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ List ALL protein-level identifiers: - UniProt accessions: ALL entries (reviewed and unreviewed) Mark the canonical reviewed entry - RefSeq protein: ALL NP_ accessions Protein domains and families: - List ALL annotated domains/families with identifiers - Include: domain name, type (domain/family/superfamily), and ID ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 4: STRUCTURE IDENTIFIERS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Experimental structures: - List ALL PDB structure IDs - For each: experimental method (X-ray, NMR, Cryo-EM) and resolution - Total PDB structure count Predicted structures: - AlphaFold model ID and confidence metrics (pLDDT) ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 5: CROSS-SPECIES ORTHOLOGS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ List orthologous genes in key model organisms (where available): - Mouse (Mus musculus): gene ID, symbol - Rat (Rattus norvegicus): gene ID, symbol - Zebrafish (Danio rerio): gene ID, symbol - Fruit fly (Drosophila melanogaster): gene ID, symbol - Worm (C. elegans): gene ID, symbol - Yeast (S. cerevisiae): gene ID, symbol ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 6: CLINICAL VARIANTS & AI PREDICTIONS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Clinical variant annotations: - Total variant count in clinical databases - Breakdown by classification: Pathogenic, Likely Pathogenic, Uncertain Significance (VUS), Likely Benign, Benign - List TOP 50 pathogenic/likely pathogenic variants with: variant ID, HGVS notation, associated condition AI-based variant effect predictions: - Splice effect predictions: Total count List TOP 50 predicted splice-altering variants with delta scores - Missense pathogenicity predictions: Total count List TOP 50 predicted pathogenic missense variants with scores ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 7: BIOLOGICAL PATHWAYS & GENE ONTOLOGY ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Pathway membership: - List ALL biological pathways this gene participates in - Include pathway IDs and names - Total pathway count Gene Ontology annotations: - Biological Process: count and TOP 20 terms with IDs - Molecular Function: count and TOP 20 terms with IDs - Cellular Component: count and TOP 20 terms with IDs ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 8: PROTEIN INTERACTIONS & MOLECULAR NETWORKS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Protein-protein interactions: - Total interaction count - List TOP 50 highest-confidence interacting proteins with scores Protein similarity (evolutionary and structural): - Structural/embedding similarity: How many similar proteins? List TOP 20 with similarity scores - Sequence homology: How many homologous proteins? List TOP 20 with identity/similarity scores ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 9: TRANSCRIPTION FACTOR REGULATORY DATA ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ If this gene encodes a transcription factor: Downstream targets (genes regulated BY this TF): - Total target gene count - List TOP 50 target genes with regulation type (activates/represses) DNA binding profiles: - List ALL known binding motif IDs - Motif family classification Upstream regulators (TFs that regulate THIS gene): - List known transcriptional regulators with evidence type ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 10: DRUG & PHARMACOLOGY DATA ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ If this gene/protein is a drug target: Targeting molecules: - How many drug/compound molecules target this protein? - List TOP 30 molecules by development phase - Include: molecule ID, name, mechanism, highest development phase Clinical trials: - How many clinical trials involve drugs targeting this gene? - List TOP 20 trials with: trial ID, phase, status, intervention Pharmacogenomics: - Known drug-gene interactions affecting drug response - Dosing guidelines if any exist ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 11: EXPRESSION PROFILES ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Tissue expression: - Which tissues express this gene most highly? - List TOP 30 tissues with expression scores/levels - Note any tissue-specific or tissue-enriched patterns Cell type expression: - Which cell types show highest expression? - List TOP 30 cell types with expression scores - Note any cell type-specific patterns Single-cell expression data (if available): - Which single-cell datasets/experiments include this gene? - Notable cell population patterns ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ SECTION 12: DISEASE ASSOCIATIONS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ Mendelian/monogenic disease links: - What diseases are caused by mutations in this gene? - List ALL associated diseases with: disease name, disease ID, inheritance pattern, evidence level Phenotype associations: - What clinical phenotypes are associated with this gene? - List TOP 50 phenotype terms with IDs Complex trait associations (GWAS): - What traits/diseases are linked via genome-wide association studies? - List TOP 30 GWAS associations with: trait, study ID, p-value, effect size if available ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ FORMATTING REQUIREMENTS ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ - Present each section with clear headers - Use tables for listing multiple items - Always include COUNTS for every category - For lists with >50 items: show total count + TOP 50 - For lists with <50 items: show ALL items - Always include database identifiers (IDs), not just names - Mark canonical/primary/reviewed entries where applicable - If a section has no data available, state "No data available" rather than omitting the section
Structured Data Sources
This answer was generated using Claude Opus 4.5 + BioBTree MCP, querying 32 biological databases.
Further analyze this answer or run your own queries with BioBTree MCP.
alphafold, alphamissense, bgee, ccds, chembl_molecule, chembl_target, clinvar, collectri, diamond_similarity, ensembl, entrez, esm2_similarity, exon, gencc, go, gwas, hgnc, hpo, intact, interpro, mim, orphanet, ortholog, pdb, pharmgkb_gene, reactome, refseq, spliceai, string_interaction, transcript, uberon, uniprotView API calls (40)
- search(NOTCH1) https://sugi.bio/biobtree/api/search?i=NOTCH1
- entry(ENSG00000148400, ensembl) https://sugi.bio/biobtree/api/entry?i=ENSG00000148400&s=ensembl
- search(NOTCH1, hgnc) https://sugi.bio/biobtree/api/search?i=NOTCH1&s=hgnc
- entry(4851, entrez) https://sugi.bio/biobtree/api/entry?i=4851&s=entrez
- entry(HGNC:7881, hgnc) https://sugi.bio/biobtree/api/entry?i=HGNC%3A7881&s=hgnc
- map(ENSG00000148400, >>ensembl>>transcript) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Etranscript
- map(ENSG00000148400, >>ensembl>>uniprot) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Euniprot
- map(HGNC:7881, >>hgnc>>mim) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Emim
- map(ENSG00000148400, >>ensembl>>refseq) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Erefseq
- map(ENSG00000148400, >>ensembl>>ccds) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Eccds
- entry(P46531, uniprot) https://sugi.bio/biobtree/api/entry?i=P46531&s=uniprot
- map(P46531, >>uniprot>>pdb) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Epdb
- map(P46531, >>uniprot>>alphafold) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ealphafold
- map(P46531, >>uniprot>>interpro) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Einterpro
- map(ENSG00000148400, >>ensembl>>ortholog) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Eortholog
- map(HGNC:7881, >>hgnc>>clinvar) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Eclinvar
- map(P46531, >>uniprot>>go) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ego
- map(P46531, >>uniprot>>go) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ego
- map(P46531, >>uniprot>>reactome) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ereactome
- map(P46531, >>uniprot>>string_interaction) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Estring_interaction
- map(P46531, >>uniprot>>intact) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Eintact
- map(P46531, >>uniprot>>alphamissense) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ealphamissense
- map(HGNC:7881, >>hgnc>>spliceai) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Espliceai
- map(HGNC:7881, >>hgnc>>collectri) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Ecollectri
- map(P46531, >>uniprot>>chembl_target) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Echembl_target
- map(CHEMBL2146346, >>chembl_target>>chembl_molecule) https://sugi.bio/biobtree/api/map?i=CHEMBL2146346&m=%3E%3Echembl_target%3E%3Echembl_molecule
- map(HGNC:7881, >>hgnc>>hpo) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Ehpo
- map(HGNC:7881, >>hgnc>>orphanet) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Eorphanet
- map(HGNC:7881, >>hgnc>>gwas) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Egwas
- map(HGNC:7881, >>hgnc>>gencc) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Egencc
- map(ENSG00000148400, >>ensembl>>bgee) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Ebgee
- map(P46531, >>uniprot>>esm2_similarity) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Eesm2_similarity
- map(P46531, >>uniprot>>diamond_similarity) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ediamond_similarity
- map(HGNC:7881, >>hgnc>>pharmgkb_gene) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Epharmgkb_gene
- map(ENSG00000148400, >>ensembl>>bgee>>uberon) https://sugi.bio/biobtree/api/map?i=ENSG00000148400&m=%3E%3Eensembl%3E%3Ebgee%3E%3Euberon
- map(HGNC:7881, >>hgnc>>clinvar[germline_classification=="Pathogenic"]) https://sugi.bio/biobtree/api/map?i=HGNC%3A7881&m=%3E%3Ehgnc%3E%3Eclinvar%5Bgermline_classification%3D%3D%22Pathogenic%22%5D
- map(P46531, >>uniprot>>alphamissense[am_class=="likely_pathogenic"]) https://sugi.bio/biobtree/api/map?i=P46531&m=%3E%3Euniprot%3E%3Ealphamissense%5Bam_class%3D%3D%22likely_pathogenic%22%5D
- entry(ENST00000651671, transcript) https://sugi.bio/biobtree/api/entry?i=ENST00000651671&s=transcript
- map(ENST00000651671, >>transcript>>exon) https://sugi.bio/biobtree/api/map?i=ENST00000651671&m=%3E%3Etranscript%3E%3Eexon
- entry(190198, mim) https://sugi.bio/biobtree/api/entry?i=190198&s=mim
Section 1: Gene Identifiers
| Database | Identifier | Notes |
|---|---|---|
| HGNC | HGNC:7881 | Approved symbol: NOTCH1 |
| HGNC Name | notch receptor 1 | Status: Approved |
| Ensembl Gene | ENSG00000148400 | |
| NCBI Entrez Gene | 4851 | |
| OMIM | 190198 | Gene/Locus |
| Attribute | Value |
|---|---|
| Chromosome | 9 |
| Cytogenetic Band | 9q34.3 |
| Start Position | 136,494,433 |
| End Position | 136,546,048 |
| Strand | Minus (-) |
| Genome Assembly | GRCh38 |
| Genomic Accession | NC_000009.12 |
Section 2: Transcript Identifiers Total Ensembl Transcripts: 17 Ensembl Transcripts (All)
| Transcript ID | Biotype | Start | End |
|---|---|---|---|
| ENST00000651671 | protein_coding | 136,494,433 | 136,546,048 |
| ENST00000680218 | protein_coding | 136,494,433 | 136,546,048 |
| ENST00000680668 | protein_coding | 136,494,433 | 136,546,048 |
| ENST00000680133 | protein_coding | 136,494,457 | 136,545,997 |
| ENST00000927794 | protein_coding | 136,494,444 | 136,545,851 |
| ENST00000680778 | protein_coding | 136,494,433 | 136,512,848 |
| ENST00000679595 | nonsense_mediated_decay | 136,494,433 | 136,546,048 |
| ENST00000680924 | nonsense_mediated_decay | 136,494,444 | 136,546,021 |
| ENST00000681135 | nonsense_mediated_decay | 136,494,433 | 136,546,048 |
| ENST00000681454 | nonsense_mediated_decay | 136,494,433 | 136,546,048 |
| ENST00000491649 | retained_intron | 136,522,572 | 136,523,898 |
| ENST00000645828 | retained_intron | 136,502,437 | 136,513,551 |
| ENST00000646957 | retained_intron | 136,510,510 | 136,513,110 |
| ENST00000679969 | retained_intron | 136,494,444 | 136,502,844 |
| ENST00000680003 | retained_intron | 136,494,444 | 136,502,695 |
| ENST00000680882 | retained_intron | 136,508,293 | 136,509,343 |
| ENST00000681298 | retained_intron | 136,495,736 | 136,508,369 |
| Accession | Type | Status | MANE Select |
|---|---|---|---|
| NM_017617 | mRNA | REVIEWED | YES (Canonical) |
| NM_001105721 | mRNA | PROVISIONAL | No |
| XM_011518717 | mRNA | PREDICTED | No |
| XM_054363009 | mRNA | PREDICTED | No |
| Accession | Status | MANE Select |
|---|---|---|
| NP_060087 | REVIEWED | YES |
| NP_001099191 | PROVISIONAL | No |
| XP_011517019 | PREDICTED | No |
| XP_054218984 | PREDICTED | No |
| CCDS ID |
|---|
| CCDS43905 |
| Exon ID | Start | End | Length |
|---|---|---|---|
| ENSE00003850181 | 136,545,726 | 136,546,048 | 322 |
| ENSE00001124718 | 136,544,024 | 136,544,102 | 78 |
| ENSE00001042401 | 136,523,717 | 136,523,979 | 262 |
| ENSE00000985020 | 136,522,850 | 136,523,188 | 338 |
| ENSE00001378880 | 136,519,443 | 136,519,565 | 122 |
| ENSE00000985022 | 136,518,591 | 136,518,824 | 233 |
| ENSE00000985023 | 136,518,137 | 136,518,292 | 155 |
| ENSE00000985024 | 136,517,752 | 136,517,937 | 185 |
| ENSE00000985025 | 136,517,272 | 136,517,385 | 113 |
| ENSE00000985026 | 136,515,981 | 136,516,094 | 113 |
| ENSE00000985027 | 136,515,483 | 136,515,716 | 233 |
| ENSE00000985028 | 136,515,290 | 136,515,400 | 110 |
| ENSE00000985029 | 136,514,510 | 136,514,702 | 192 |
| ENSE00000985030 | 136,513,392 | 136,513,537 | 145 |
| ENSE00000985031 | 136,513,021 | 136,513,134 | 113 |
| ENSE00000985032 | 136,511,152 | 136,511,271 | 119 |
| ENSE00000985033 | 136,510,653 | 136,510,805 | 152 |
| ENSE00000985034 | 136,509,733 | 136,509,961 | 228 |
| ENSE00000985035 | 136,508,870 | 136,509,071 | 201 |
| ENSE00000985036 | 136,508,232 | 136,508,385 | 153 |
| ENSE00000985037 | 136,507,955 | 136,508,139 | 184 |
| ENSE00000985038 | 136,507,305 | 136,507,437 | 132 |
| ENSE00000985039 | 136,506,716 | 136,506,973 | 257 |
| ENSE00000985040 | 136,506,527 | 136,506,639 | 112 |
| ENSE00000985041 | 136,505,310 | 136,505,881 | 571 |
| ENSE00000985042 | 136,504,673 | 136,505,104 | 431 |
| ENSE00003681600 | 136,503,182 | 136,503,330 | 148 |
| ENSE00000985044 | 136,502,272 | 136,502,488 | 216 |
| ENSE00000985045 | 136,502,001 | 136,502,088 | 87 |
| ENSE00000985046 | 136,501,748 | 136,501,913 | 165 |
| ENSE00000985047 | 136,500,552 | 136,500,847 | 295 |
| ENSE00000985048 | 136,499,112 | 136,499,259 | 147 |
| ENSE00000985049 | 136,498,899 | 136,498,996 | 97 |
| ENSE00001247584 | 136,494,433 | 136,497,558 | 3,125 |
Section 3: Protein Identifiers UniProt Accessions (Total: 9)
| Accession | Type | Notes |
|---|---|---|
| P46531 | Reviewed (Swiss-Prot) | CANONICAL |
| A0A7P0T8U6 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0T8W1 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0T9V1 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0TA56 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0TAK8 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0TB20 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0TBG2 | Unreviewed (TrEMBL) | Isoform |
| A0A7P0Z4H9 | Unreviewed (TrEMBL) | Isoform |
| Property | Value |
|---|---|
| Name | Neurogenic locus notch homolog protein 1 |
| Alternative Name | Translocation-associated notch protein TAN-1 |
| Length | 2,555 amino acids |
| Mass | 272,505 Da |
| InterPro ID | Name | Type |
|---|---|---|
| IPR008297 | Notch | Family |
| IPR022362 | Notch_1 | Family |
| IPR051355 | Notch/Slit_guidance | Family |
| IPR000742 | EGF | Domain |
| IPR000800 | Notch_dom | Domain |
| IPR001881 | EGF-like_Ca-bd_dom | Domain |
| IPR010660 | Notch_NOD_dom | Domain |
| IPR011656 | Notch_NODP_dom | Domain |
| IPR024600 | Notch_C | Domain |
| IPR049883 | NOTCH1_EGF-like | Domain |
| IPR002110 | Ankyrin_rpt | Repeat |
| IPR009030 | Growth_fac_rcpt_cys_sf | Homologous superfamily |
| IPR035993 | Notch-like_dom_sf | Homologous superfamily |
| IPR036770 | Ankyrin_rpt-contain_sf | Homologous superfamily |
| IPR000152 | EGF-type_Asp/Asn_hydroxyl_site | PTM |
| IPR013032 | EGF-like_CS | Conserved site |
| IPR018097 | EGF_Ca-bd_CS | Conserved site |
Section 4: Structure Identifiers Experimental Structures - Total PDB Count: 29
| PDB ID | Method | Resolution | Title |
|---|---|---|---|
| 1PB5 | NMR | - | NMR Structure of a Prototype LNR Module from Human Notch1 |
| 1TOZ | NMR | - | NMR structure of the human NOTCH-1 ligand binding region |
| 1YYH | X-ray | 1.90 Å | Crystal structure of the human Notch 1 ankyrin domain |
| 2F8X | X-ray | 3.25 Å | Crystal structure of activated Notch, CSL and MAML on HES-1 promoter DNA |
| 2F8Y | X-ray | 1.55 Å | Crystal structure of human Notch1 ankyrin repeats |
| 2HE0 | X-ray | 1.90 Å | Crystal structure of a human Notch1 ankyrin domain mutant |
| 2VJ3 | X-ray | 2.60 Å | Human Notch-1 EGFs 11-13 |
| 3ETO | X-ray | 2.00 Å | 2 Angstrom X-ray structure of the NOTCH1 Negative Regulatory Region |
| 3I08 | X-ray | 3.20 Å | Crystal structure of the S1-cleaved Notch1 NRR |
| 3L95 | X-ray | 2.19 Å | Crystal structure of human Notch1 NRR bound to antagonist antibody |
| 3NBN | X-ray | 3.45 Å | Crystal structure of a dimer of Notch Transcription Complex |
| 3V79 | X-ray | 3.85 Å | Structure of human Notch1 transcription complex |
| 4CUD | X-ray | 1.85 Å | Human Notch1 EGF domains 11-13 mutant fucosylated at T466 |
| 4CUE | X-ray | 3.00 Å | Human Notch1 EGF domains 11-13 mutant T466V |
| 4CUF | X-ray | 2.29 Å | Human Notch1 EGF domains 11-13 mutant T466S |
| 4D0E | X-ray | 1.61 Å | Human Notch1 EGF domains 11-13 with GlcNAc-fucose |
| 4D0F | X-ray | 2.80 Å | Human Notch1 EGF domains 11-13 mutant T466A |
| 5FM9 | X-ray | 2.92 Å | Human Notch 1, EGF 4-7 |
| 5FMA | X-ray | 2.46 Å | Human Notch 1, EGF 4-7 |
| 5KZO | NMR | - | Notch1 transmembrane and juxtamembrane segment |
| 5L0R | X-ray | 1.50 Å | Human POGLUT1 in complex with Notch1 EGF12 |
| 5UB5 | X-ray | 2.09 Å | Human POGLUT1 in complex with human Notch1 EGF12 S458T mutant |
| 6IDF | Cryo-EM | 2.70 Å | Cryo-EM structure of gamma secretase in complex with Notch fragment |
| 6PY8 | X-ray | 3.75 Å | Crystal structure of RBPJ-NOTCH1-NRARP ternary complex |
| 8OR5 | NMR | - | Solution NMR structure of Notch1 TMD |
| 8ORY | NMR | - | Solution NMR structure of Notch1 L1740-1743 TMD |
| 8ORZ | NMR | - | Solution NMR structure of Notch1 G1740-1743 TMD |
| 9B3G | X-ray | 1.55 Å | Human Notch-1 EGFs 21-23 |
| 9B3N | X-ray | 1.50 Å | Human Notch-1 EGFs 20-24 |
| Model ID | Sequence Length | Global pLDDT | Fraction Very High Confidence |
|---|---|---|---|
| P46531 | 18,917 fragments | 59.74 | 0.03 (3%) |
Section 5: Cross-Species Orthologs
| Organism | Gene ID | Symbol | Biotype |
|---|---|---|---|
| Mouse (Mus musculus) | ENSMUSG00000026923 | Notch1 | protein_coding |
| Rat (Rattus norvegicus) | ENSRNOG00000019322 | Notch1 | protein_coding |
| Zebrafish (Danio rerio) | ENSDARG00000052094 | notch1b | protein_coding |
| Zebrafish (Danio rerio) | ENSDARG00000103554 | notch1a | protein_coding |
| Fruit fly (Drosophila melanogaster) | No direct ortholog | - | Ancestral Notch gene |
| Worm (C. elegans) | No direct ortholog | - | lin-12, glp-1 related |
| Yeast (S. cerevisiae) | No ortholog | - | - |
Section 6: Clinical Variants & AI Predictions ClinVar Variant Summary Total Variants in ClinVar: 4,156
| Classification | Count |
|---|---|
| Pathogenic | 85 |
| Likely Pathogenic | ~100+ |
| Uncertain Significance (VUS) | ~2,500+ |
| Likely Benign | ~500+ |
| Benign | ~200+ |
| Conflicting Classifications | ~500+ |
| Variant ID | HGVS Notation | Type | Review Status |
|---|---|---|---|
| 521568 | c.166C>T (p.Arg56Ter) | SNV | Multiple submitters |
| 645087 | c.550C>T (p.Gln184Ter) | SNV | Single submitter |
| 221999 | c.578G>A (p.Gly193Asp) | SNV | No assertion criteria |
| 1428655 | c.428del (p.Pro143fs) | Deletion | Multiple submitters |
| 523583 | c.415C>T (p.Gln139Ter) | SNV | Single submitter |
| 2123517 | c.410C>A (p.Ser137Ter) | SNV | Single submitter |
| 219375 | c.1343G>A (p.Arg448Gln) | SNV | Single submitter |
| 572044 | c.1396del (p.Thr466fs) | Deletion | Single submitter |
| 2636214 | c.1537C>T (p.Gln513Ter) | SNV | Multiple submitters |
| 219378 | c.1649dup (p.Tyr550Ter) | Dup | Single submitter |
| 3340288 | c.1650C>G (p.Tyr550Ter) | SNV | Single submitter |
| 1453811 | c.763_773del (p.Glu255fs) | Deletion | Single submitter |
| 523584 | c.794_797delinsCC (p.Asn265fs) | Indel | Single submitter |
| 845149 | c.1017_1018del (p.Ala340fs) | Deletion | Single submitter |
| 4293949 | c.873C>G (p.Tyr291Ter) | SNV | Single submitter |
| 1075050 | c.1784_1787del (p.Tyr595fs) | Deletion | Single submitter |
| 1409179 | c.1800_1801dup (p.Glu601fs) | Dup | Single submitter |
| 3658668 | c.1847del (p.Gly616fs) | Deletion | Single submitter |
| 4635489 | c.1896del (p.Thr633fs) | Deletion | Single submitter |
| 3340287 | c.1904-2A>G | Splice | Single submitter |
| 523585 | c.1935_1936del (p.Ala646fs) | Deletion | Single submitter |
| 4687945 | c.1987G>T (p.Glu663Ter) | SNV | Single submitter |
| 422753 | c.2023del (p.Cys675fs) | Deletion | Single submitter |
| 1344870 | c.2155G>T (p.Glu719Ter) | SNV | No criteria |
| 1344732 | c.2272G>T (p.Glu758Ter) | SNV | No criteria |
| 3235929 | c.2278_2282del (p.Asn760fs) | Deletion | Single submitter |
| 544178 | c.2365C>T (p.Gln789Ter) | SNV | Multiple submitters |
| 523594 | c.2380G>T (p.Glu794Ter) | SNV | Single submitter |
| 3027324 | c.2407C>T (p.Gln803Ter) | SNV | Single submitter |
| 2633308 | c.2436del (p.Tyr813fs) | Deletion | Single submitter |
| 221998 | c.2439C>G (p.Tyr813Ter) | SNV | Single submitter |
| 817997 | c.2448dup (p.Cys817fs) | Dup | Multiple submitters |
| 2631128 | c.2536C>T (p.Gln846Ter) | SNV | Single submitter |
| 1961662 | c.2759dup (p.Ser921fs) | Dup | Single submitter |
| 2695701 | c.2880C>A (p.Cys960Ter) | SNV | Single submitter |
| 520577 | c.3052del (p.Cys1018fs) | Deletion | Single submitter |
| 523596 | c.3281G>A (p.Cys1094Tyr) | SNV | Single submitter |
| 544179 | c.3266G>A (p.Trp1089Ter) | SNV | Single submitter |
| 4291131 | c.3316C>T (p.Gln1106Ter) | SNV | Single submitter |
| 12476 | c.3319C>T (p.Arg1107Ter) | SNV | Multiple submitters |
| 3345218 | c.3332_3347del (p.Asp1111fs) | Deletion | Single submitter |
| 1344783 | c.3463C>T (p.Gln1155Ter) | SNV | No criteria |
| 3389911 | c.3656_3666del (p.Glu1219fs) | Deletion | Single submitter |
| 2671929 | c.3684del (p.Val1229fs) | Deletion | Multiple submitters |
| 221997 | c.3765C>A (p.Cys1255Ter) | SNV | No criteria |
| 2843383 | c.3792_3793del (p.Cys1264_Glu1265delins*) | Deletion | Single submitter |
| 3880477 | c.3909_3919del (p.Cys1304fs) | Deletion | Single submitter |
| 2822065 | c.4021G>T (p.Glu1341Ter) | SNV | Single submitter |
| 566177 | c.4071C>A (p.Cys1357Ter) | SNV | Single submitter |
| 642523 | c.4127del (p.Gly1376fs) | Deletion | Single submitter |
| Classification | Approximate Count |
|---|---|
| Likely Pathogenic | ~4,000+ |
| Ambiguous | ~3,000+ |
| Likely Benign | ~9,000+ |
| Variant | Protein Change | Pathogenicity Score | Class |
|---|---|---|---|
| 9:136496143:C:A | W2532C | 0.994 | likely_pathogenic |
| 9:136496143:C:G | W2532C | 0.994 | likely_pathogenic |
| 9:136496179:C:A | W2520C | 0.991 | likely_pathogenic |
| 9:136496179:C:G | W2520C | 0.991 | likely_pathogenic |
| 9:136496181:A:G | W2520R | 0.991 | likely_pathogenic |
| 9:136496181:A:T | W2520R | 0.991 | likely_pathogenic |
| 9:136496145:A:G | W2532R | 0.990 | likely_pathogenic |
| 9:136496145:A:T | W2532R | 0.990 | likely_pathogenic |
| 9:136496125:G:C | S2538R | 0.984 | likely_pathogenic |
| 9:136496125:G:T | S2538R | 0.984 | likely_pathogenic |
| 9:136496173:G:C | S2522R | 0.982 | likely_pathogenic |
| 9:136496173:G:T | S2522R | 0.982 | likely_pathogenic |
| 9:136496212:G:C | F2509L | 0.980 | likely_pathogenic |
| 9:136496212:G:T | F2509L | 0.980 | likely_pathogenic |
| 9:136496213:A:C | F2509C | 0.968 | likely_pathogenic |
| 9:136496141:G:A | S2533F | 0.937 | likely_pathogenic |
| 9:136496148:C:G | D2531H | 0.934 | likely_pathogenic |
| 9:136496201:G:T | S2513Y | 0.932 | likely_pathogenic |
| 9:136496210:A:T | L2510H | 0.928 | likely_pathogenic |
| 9:136496147:A:C | D2531V | 0.924 | likely_pathogenic |
| 9:136496201:G:A | S2513F | 0.921 | likely_pathogenic |
| 9:136496213:A:G | F2509S | 0.920 | likely_pathogenic |
| 9:136496201:G:C | S2513C | 0.916 | likely_pathogenic |
| 9:136496142:A:G | S2533P | 0.910 | likely_pathogenic |
| 9:136496141:G:T | S2533Y | 0.898 | likely_pathogenic |
| 9:136496207:G:A | T2511I | 0.896 | likely_pathogenic |
| 9:136496180:C:A | W2520L | 0.895 | likely_pathogenic |
| 9:136496204:G:T | P2512Q | 0.890 | likely_pathogenic |
| 9:136496147:T:G | D2531A | 0.890 | likely_pathogenic |
| 9:136496141:G:C | S2533C | 0.886 | likely_pathogenic |
| 9:136496210:A:G | L2510P | 0.886 | likely_pathogenic |
| 9:136496148:C:A | D2531Y | 0.885 | likely_pathogenic |
| 9:136496177:G:A | S2521F | 0.851 | likely_pathogenic |
| 9:136496207:G:T | T2511N | 0.851 | likely_pathogenic |
| 9:136496147:T:C | D2531G | 0.852 | likely_pathogenic |
| 9:136496202:A:G | S2513P | 0.842 | likely_pathogenic |
| 9:136496198:G:T | P2514H | 0.833 | likely_pathogenic |
| 9:136496145:A:C | W2520G | 0.799 | likely_pathogenic |
| 9:136496204:G:A | P2512L | 0.792 | likely_pathogenic |
| 9:136496177:G:C | S2521C | 0.791 | likely_pathogenic |
| 9:136496138:T:A | E2534V | 0.776 | likely_pathogenic |
| 9:136496198:G:C | P2514R | 0.764 | likely_pathogenic |
| 9:136496208:T:C | T2511A | 0.758 | likely_pathogenic |
| 9:136496168:G:T | S2524Y | 0.757 | likely_pathogenic |
| 9:136496150:G:C | S2530C | 0.752 | likely_pathogenic |
| 9:136496174:C:T | S2522N | 0.740 | likely_pathogenic |
| 9:136496174:C:A | S2522I | 0.739 | likely_pathogenic |
| 9:136496199:G:A | P2514S | 0.735 | likely_pathogenic |
| 9:136496146:G:C | D2531E | 0.733 | likely_pathogenic |
| 9:136496168:G:A | S2524F | 0.731 | likely_pathogenic |
| Variant | Effect | Delta Score |
|---|---|---|
| 9:136497557:TCC:T | acceptor_loss | 1.000 |
| 9:136497560:T:A | acceptor_loss | 1.000 |
| 9:136497558:CCT:C | acceptor_loss | 1.000 |
| 9:136497554:TCCTC:T | acceptor_gain | 0.990 |
| 9:136497555:CCTCC:C | acceptor_gain | 0.990 |
| 9:136497556:CTC:C | acceptor_gain | 0.990 |
| 9:136497559:C:CC | acceptor_gain | 0.990 |
| 9:136497557:TC:T | acceptor_gain | 0.980 |
| 9:136497558:CC:C | acceptor_gain | 0.980 |
| 9:136497566:A:AC | acceptor_gain | 0.980 |
| 9:136497566:A:C | acceptor_gain | 0.980 |
| 9:136497905:T:TA | donor_gain | 0.950 |
| 9:136497555:CCTC:C | acceptor_gain | 0.930 |
| 9:136497557:TCCT:T | acceptor_gain | 0.930 |
| 9:136497556:CTCC:C | acceptor_gain | 0.930 |
| 9:136497558:C:G | acceptor_gain | 0.910 |
| 9:136497875:C:A | donor_gain | 0.820 |
| 9:136497559:C:T | acceptor_gain | 0.760 |
| 9:136497554:TCC:T | acceptor_gain | 0.750 |
| 9:136495700:T:C | acceptor_gain | 0.720 |
| 9:136497573:C:CT | acceptor_gain | 0.680 |
| 9:136497538:C:CT | acceptor_gain | 0.660 |
| 9:136495700:T:TC | acceptor_gain | 0.650 |
| 9:136497922:G:C | donor_gain | 0.630 |
| 9:136497527:TCCCG:T | acceptor_gain | 0.530 |
| 9:136497559:C:G | acceptor_gain | 0.530 |
| 9:136497561:G:C | acceptor_loss | 0.510 |
| 9:136497855:A:T | donor_gain | 0.470 |
| 9:136497556:C:T | acceptor_gain | 0.460 |
| 9:136497528:C:G | acceptor_gain | 0.440 |
| 9:136497906:C:A | donor_gain | 0.440 |
| 9:136498278:TCTGC:T | donor_gain | 0.440 |
| 9:136497574:G:T | acceptor_gain | 0.430 |
| 9:136497852:T:TA | donor_gain | 0.420 |
| 9:136497903:ATT:A | donor_gain | 0.420 |
| 9:136497560:T:TC | acceptor_gain | 0.420 |
| 9:136497631:C:CT | acceptor_gain | 0.420 |
| 9:136497918:CAGAG:C | donor_gain | 0.410 |
| 9:136497986:C:CT | donor_gain | 0.400 |
| 9:136497928:G:T | donor_gain | 0.380 |
| 9:136497874:T:TA | donor_gain | 0.380 |
| 9:136497530:C:CT | acceptor_gain | 0.370 |
| 9:136497902:AATT:A | donor_gain | 0.370 |
| 9:136497719:AG:A | donor_gain | 0.360 |
| 9:136497480:G:T | acceptor_gain | 0.360 |
| 9:136497902:A:T | donor_gain | 0.360 |
| 9:136497531:G:T | acceptor_gain | 0.350 |
| 9:136497901:AAATT:A | donor_gain | 0.340 |
| 9:136497860:A:AC | donor_gain | 0.340 |
| 9:136497861:C:CC | donor_gain | 0.340 |
Section 7: Biological Pathways & Gene Ontology Reactome Pathways - Total: 20
| Pathway ID | Pathway Name | Disease Pathway |
|---|---|---|
| R-HSA-1912399 | Pre-NOTCH Processing in the Endoplasmic Reticulum | No |
| R-HSA-1912408 | Pre-NOTCH Transcription and Translation | No |
| R-HSA-1912420 | Pre-NOTCH Processing in Golgi | No |
| R-HSA-210744 | Regulation of gene expression in late stage pancreatic bud | No |
| R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | No |
| R-HSA-2122948 | Activated NOTCH1 Transmits Signal to the Nucleus | No |
| R-HSA-350054 | Notch-HLH transcription pathway | No |
| R-HSA-8941856 | RUNX3 regulates NOTCH signaling | No |
| R-HSA-9013508 | NOTCH3 Intracellular Domain Regulates Transcription | No |
| R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | No |
| R-HSA-9793380 | Formation of paraxial mesoderm | No |
| R-HSA-9818030 | NFE2L2 regulating tumorigenic genes | No |
| R-HSA-9818749 | Regulation of NFE2L2 gene expression | No |
| R-HSA-9824272 | Somitogenesis | No |
| R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | Yes |
| R-HSA-2644607 | Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling | Yes |
| R-HSA-2660826 | Constitutive Signaling by NOTCH1 t(7;9) Translocation Mutant | Yes |
| R-HSA-2691232 | Constitutive Signaling by NOTCH1 HD Domain Mutants | Yes |
| R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | Yes |
| R-HSA-5083630 | Defective LFNG causes SCDO3 | Yes |
| GO ID | Term Name |
|---|---|
| GO:0007219 | Notch signaling pathway |
| GO:0007221 | positive regulation of transcription of Notch receptor target |
| GO:0045747 | positive regulation of Notch signaling pathway |
| GO:0007507 | heart development |
| GO:0003180 | aortic valve morphogenesis |
| GO:0003181 | atrioventricular valve morphogenesis |
| GO:0003184 | pulmonary valve morphogenesis |
| GO:0003198 | epithelial to mesenchymal transition in endocardial cushion |
| GO:0060317 | cardiac epithelial to mesenchymal transition |
| GO:0001837 | epithelial to mesenchymal transition |
| GO:0002040 | sprouting angiogenesis |
| GO:0060842 | arterial endothelial cell differentiation |
| GO:0060843 | venous endothelial cell differentiation |
| GO:0045944 | positive regulation of transcription by RNA polymerase II |
| GO:0000122 | negative regulation of transcription by RNA polymerase II |
| GO:0048708 | astrocyte differentiation |
| GO:0048709 | oligodendrocyte differentiation |
| GO:0030216 | keratinocyte differentiation |
| GO:0035914 | skeletal muscle cell differentiation |
| GO:0008284 | positive regulation of cell population proliferation |
| GO ID | Term Name |
|---|---|
| GO:0004888 | transmembrane signaling receptor activity |
| GO:0005112 | Notch binding |
| GO:0005509 | calcium ion binding |
| GO:0003713 | transcription coactivator activity |
| GO:0140537 | transcription regulator activator activity |
| GO:0031490 | chromatin DNA binding |
| GO:0019899 | enzyme binding |
| GO:0004857 | enzyme inhibitor activity |
| GO:0042802 | identical protein binding |
| GO ID | Term Name |
|---|---|
| GO:0005886 | plasma membrane |
| GO:0016324 | apical plasma membrane |
| GO:0009986 | cell surface |
| GO:0005634 | nucleus |
| GO:0005654 | nucleoplasm |
| GO:0005829 | cytosol |
| GO:0005789 | endoplasmic reticulum membrane |
| GO:0000139 | Golgi membrane |
| GO:0010008 | endosome membrane |
| GO:0031902 | late endosome membrane |
| GO:0002193 | MAML1-RBP-Jkappa-ICN1 complex |
| GO:0043235 | receptor complex |
| GO:0005912 | adherens junction |
| GO:0005576 | extracellular region |
| GO:0098978 | glutamatergic synapse |
| GO:0098839 | postsynaptic density membrane |
| GO:0098685 | Schaffer collateral - CA1 synapse |
| GO:0001669 | acrosomal vesicle |
Section 8: Protein Interactions & Molecular Networks Protein-Protein Interactions STRING Interactions Total: 6,600 IntAct Interactions Total: 220 BioGRID Interactions Total: 591 TOP 50 Highest-Confidence STRING Interacting Proteins
| UniProt ID | Score | Protein Name |
|---|---|---|
| P46531 | 999 | NOTCH1 (self) |
| Q06330 | 999 | RBPJ (Recombining binding protein suppressor of hairless) |
| Q92585 | 998 | MAML1 (Mastermind-like protein 1) |
| Q96JK9 | 996 | MAML3 |
| Q8IZL2 | 995 | MAML2 |
| O00548 | 988 | DLL1 (Delta-like protein 1) |
| P78504 | 988 | JAG1 (Jagged-1) |
| Q9NR61 | 988 | DLL4 (Delta-like protein 4) |
| Q9Y219 | 988 | JAG2 (Jagged-2) |
| Q9NYJ7 | 987 | DLL3 (Delta-like protein 3) |
| Q15063 | 970 | PSEN1 (Presenilin-1) |
| Q9BXP5 | 960 | ADAM10 |
| P84022 | 943 | SMAD3 |
| P35222 | 932 | CTNNB1 (Beta-catenin) |
| Q16665 | 918 | HIF1A |
| Q9Y6R0 | 891 | NUMB |
| Q969H0 | 885 | FBXW7 |
| P49768 | 884 | PSEN2 (Presenilin-2) |
| Q9Y5J3 | 881 | TSPAN12 |
| P00533 | 873 | EGFR |
| Q5TA89 | 872 | MFNG (Beta-1,3-N-acetylglucosaminyltransferase manic fringe) |
| Q9UBP5 | 865 | HES5 |
| Q86Y01 | 850 | RFNG |
| P49757 | 849 | NUMB-like protein |
| P19838 | 809 | NFKB1 |
| Q13485 | 809 | SMAD4 |
| P01106 | 801 | MYC |
| P24385 | 801 | CCND1 (Cyclin D1) |
| P25942 | 799 | CD40 |
| P04626 | 787 | ERBB2 |
| P04637 | 787 | TP53 |
| Q96T58 | 775 | MFAP5 |
| P48745 | 766 | NOV (Nephroblastoma overexpressed gene protein) |
| P05067 | 762 | APP |
| P31749 | 757 | AKT1 |
| P16070 | 749 | CD44 |
| P25490 | 745 | TLE1 |
| Q7Z6K4 | 745 | LFNG |
| P09325 | 741 | SFRP4 |
| P60484 | 737 | PTEN |
| P11362 | 736 | FGFR1 |
| Q96BI3 | 727 | APH1A |
| Q14469 | 725 | HES1 |
| Q9UJU2 | 725 | LEF1 |
| P18443 | 723 | RBX1 |
| P49841 | 723 | GSK3B |
| P28908 | 721 | TNFRSF8 |
| P48436 | 717 | SOX9 |
| Q8NES3 | 713 | LFNG |
| P42336 | 700 | PIK3CA |
| Interaction ID | Partner Gene | Interaction Type | Score |
|---|---|---|---|
| EBI-15698611 | MAML1 | physical association | 0.950 |
| EBI-15814834 | MAML1 | association | 0.950 |
| EBI-15886410 | MAML1 | physical association | 0.950 |
| EBI-15886435 | MAML1 | direct interaction | 0.950 |
| EBI-15968507 | MAML1 | physical association | 0.950 |
| EBI-26972890 | MAML1 | physical association | 0.950 |
| EBI-15621512 | RBPJ | association | 0.910 |
| EBI-15662645 | FBXW7 | association | 0.880 |
| EBI-15662673 | FBXW7 | direct interaction | 0.880 |
| EBI-15876051 | FBXW7 | physical association | 0.880 |
| EBI-16125085 | FBXW7 | physical association | 0.880 |
| EBI-16125142 | FBXW7 | physical association | 0.880 |
| EBI-16125197 | FBXW7 | physical association | 0.880 |
| EBI-16125238 | FBXW7 | physical association | 0.880 |
| EBI-16125275 | FBXW7 | physical association | 0.880 |
| EBI-15814808 | RBPJ | association | 0.740 |
| EBI-15814856 | RBPJ | direct interaction | 0.740 |
| EBI-15814877 | RBPJ | direct interaction | 0.740 |
| EBI-15968483 | RBPJ | direct interaction | 0.740 |
| EBI-15968534 | RBPJ | direct interaction | 0.740 |
| EBI-15968557 | RBPJ | direct interaction | 0.740 |
| EBI-15718282 | JAG1 | direct interaction | 0.730 |
| EBI-15718305 | JAG1 | direct interaction | 0.730 |
| EBI-15718326 | JAG1 | direct interaction | 0.730 |
| EBI-15718354 | JAG1 | direct interaction | 0.730 |
| EBI-16154871 | ATM | physical association | 0.660 |
| EBI-16154888 | ATM | physical association | 0.660 |
| EBI-16154928 | ATM | physical association | 0.660 |
| EBI-16154945 | ATM | physical association | 0.660 |
| EBI-16154988 | ATM | direct interaction | 0.660 |
| EBI-13916003 | KDM1A | association | 0.560 |
| EBI-13916171 | KDM1A | association | 0.560 |
| EBI-13916205 | KDM1A | physical association | 0.560 |
| EBI-13916240 | KDM1A | association | 0.560 |
| EBI-13916258 | KDM1A | association | 0.560 |
| EBI-13916271 | KDM1A | association | 0.560 |
| EBI-13916303 | KDM1A | association | 0.560 |
| EBI-26972899 | MAML3 | physical association | 0.550 |
| EBI-15698630 | HIF1A | physical association | 0.500 |
| EBI-15698649 | HIF1A | association | 0.500 |
| EBI-13916178 | PHF8 | association | 0.460 |
| EBI-13916185 | SMARCA4 | association | 0.460 |
| EBI-13916287 | SMARCA4 | association | 0.460 |
| EBI-13916322 | MAPK1 | association | 0.460 |
| EBI-13916342 | RBBP4 | association | 0.460 |
| EBI-13916352 | PRKDC | association | 0.460 |
| EBI-11473706 | HIF1AN | hydroxylation reaction | 0.440 |
| EBI-11510948 | LILRB2 | physical association | 0.400 |
| EBI-21398082 | NOTCH1 | physical association (homo) | 0.400 |
| EBI-27039608 | ABL1 | physical association | 0.370 |
| UniProt ID | Top Similarity | Avg Similarity | Protein |
|---|---|---|---|
| Q01705 | 0.9998 | 0.9785 | NOTCH2 (Human) |
| Q07008 | 0.9998 | 0.9785 | NOTCH3 (Human) |
| O35516 | 0.9998 | 0.9792 | Notch1 (Mouse) |
| Q9QW30 | 0.9998 | 0.9795 | Notch1 (Mouse) |
| Q61982 | 0.9997 | 0.9735 | Notch2 (Mouse) |
| R9172 | 0.9997 | 0.9727 | Notch3 (Mouse) |
| A2RUV0 | 0.9996 | 0.9758 | Notch1 (Zebrafish) |
| P21783 | 0.9996 | 0.9758 | Notch (Drosophila) |
| Q5ZQU0 | 0.9999 | 0.9829 | Notch1 (Chicken) |
| Q70E20 | 0.9999 | 0.9829 | Notch1 (Chicken) |
| Q04721 | 0.9994 | 0.9793 | Notch2 |
| G3I6Z6 | 0.9993 | 0.9794 | Notch1 |
| A0A096LNW5 | 0.9986 | 0.9797 | Notch1 isoform |
| P0DPK3 | 0.9986 | 0.9798 | Notch1 isoform |
| Q9UM47 | 0.9986 | 0.9689 | NOTCH4 (Human) |
| Q8TER0 | 0.9984 | 0.9818 | Notch1 |
| Q31695 | 0.9980 | 0.9687 | Notch |
| Q99466 | 0.9980 | 0.9632 | NOTCH4 |
| P46530 | 0.9965 | 0.9773 | NOTCH2 |
| Q7Z3S9 | 0.9956 | 0.9796 | NOTCH3 |
| UniProt ID | Top Identity % | Protein |
|---|---|---|
| B4DH59 | 100.0 | NOTCH1 isoform |
| A0A096LNW5 | 100.0 | NOTCH1 isoform |
| P0DPK3 | 100.0 | NOTCH1 isoform |
| Q01705 | 98.9 | NOTCH2 (Human) |
| Q07008 | 98.9 | NOTCH3 (Human) |
| G3I6Z6 | 97.5 | Notch1 |
| O35516 | 96.3 | Notch1 (Mouse) |
| Q9QW30 | 96.3 | Notch1 (Mouse) |
| Q6RI86 | 96.8 | Notch1 |
| Q61982 | 94.9 | Notch2 (Mouse) |
| Q9P2R3 | 94.9 | NOTCH4 |
| Q810B6 | 94.9 | Notch1 |
| A2VCU8 | 93.7 | Notch1 |
| Q7ZXL5 | 93.7 | Notch1 |
| Q92832 | 93.6 | Notch2 |
| A2RUV0 | 92.2 | Notch1 |
| P21783 | 92.2 | Notch (Drosophila) |
| Q9UM47 | 91.0 | NOTCH4 (Human) |
Section 9: Transcription Factor Regulatory Data NOTCH1 intracellular domain (NICD) functions as a transcriptional co-activator Upstream Regulators (TFs that regulate NOTCH1) - Total: 254
| TF Gene | Regulation | Confidence |
|---|---|---|
| BCL11B | Activation | High |
| CTNNB1 | Activation | High |
| GATA5 | Activation | Low |
| KLF5 | Activation | Low |
| LEF1 | Activation | - |
| MAML1 | Activation | - |
| MAML2 | Activation | - |
| BMP2 | Activation | - |
| CD46 | Activation | - |
| CGA | Activation | - |
| FSHB | Activation | - |
| FOXO3 | Repression | - |
| IKZF1 | Repression | Low |
| MECP2 | Repression | - |
| MESP2 | Repression | - |
| AHR | Unknown | High |
| AP1 | Unknown | High |
| AR | Unknown | High |
| CEBPB | Unknown | High |
| CEBPD | Unknown | High |
| CREB1 | Unknown | High |
| CREM | Unknown | High |
| CRX | Unknown | High |
| CTBP2 | Unknown | High |
| DLX4 | Unknown | High |
| EGR1 | Unknown | High |
| ESR1 | Unknown | High |
| ESR2 | Unknown | High |
| ETS2 | Unknown | High |
| ETV4 | Unknown | High |
| EZH2 | Unknown | High |
| FOS | Unknown | High |
| FOXA2 | Unknown | High |
| FOXN1 | Unknown | High |
| FOXO1 | Unknown | High |
| GATA4 | Unknown | High |
| GLI3 | Unknown | High |
| GRHL3 | Unknown | High |
| HES1 | Unknown | High |
| HES5 | Unknown | High |
| HIF1A | Unknown | High |
| ID2 | Unknown | High |
| ID3 | Unknown | High |
| IRF1 | Unknown | High |
| ISL1 | Unknown | High |
| JARID2 | Unknown | High |
| JUN | Unknown | High |
| JUNB | Unknown | High |
| JUND | Unknown | High |
| KAT7 | Unknown | High |
- HES1, HES5, HES7 (Hairy/Enhancer of Split family)
- HEY1, HEY2, HEYL (Hairy/Enhancer of Split related)
- MYC
- CCND1 (Cyclin D1)
- CDKN1A (p21)
- NRARP
Section 10: Drug & Pharmacology Data ChEMBL Target Information
| Target ID | Target Name | Type |
|---|---|---|
| CHEMBL2146346 | Neurogenic locus notch homolog protein 1 | SINGLE PROTEIN |
| CHEMBL4524007 | Notch receptor | PROTEIN FAMILY |
| ChEMBL ID | Name | Type | Highest Phase |
|---|---|---|---|
| CHEMBL3911164 | VAREGACESTAT | Small molecule | Phase 2 |
| CHEMBL360322 | - | Small molecule | Phase 0 |
| CHEMBL3604460 | - | Small molecule | Phase 0 |
| CHEMBL3890931 | - | Small molecule | Phase 0 |
| CHEMBL3891599 | - | Small molecule | Phase 0 |
| CHEMBL3893305 | - | Small molecule | Phase 0 |
| (100+ additional compounds in preclinical) | - | Small molecule | Phase 0 |
| Attribute | Value |
|---|---|
| PharmGKB ID | PA31683 |
| Symbol | NOTCH1 |
| VIP Gene | Yes |
| CPIC Guideline | No |
| Chromosome | chr9 |
- Glucocorticoids (in T-ALL)
- CDK4/6 inhibitors
- PI3K inhibitors
Section 11: Expression Profiles Bgee Expression Summary
| Property | Value |
|---|---|
| Expression Breadth | Ubiquitous |
| Total Present Calls | 272 |
| Max Expression Score | 97.85 |
| Tissue (UBERON) | Tissue Name |
|---|---|
| UBERON:0000178 | Blood |
| UBERON:0002370 | Thymus |
| UBERON:0002106 | Spleen |
| UBERON:0002372 | Tonsil |
| UBERON:0002048 | Lung |
| UBERON:0008949 | Lower lobe of lung |
| UBERON:0008948 | Upper lobe of lung |
| UBERON:0001043 | Esophagus |
| UBERON:0002469 | Esophagus mucosa |
| UBERON:0001160 | Fundus of stomach |
| UBERON:0001199 | Mucosa of stomach |
| UBERON:0001155 | Colon |
| UBERON:0000317 | Colonic mucosa |
| UBERON:0001157 | Transverse colon |
| UBERON:0000160 | Intestine |
| UBERON:0000059 | Large intestine |
| UBERON:0001153 | Caecum |
| UBERON:0002098 | Apex of heart |
| UBERON:0001911 | Mammary gland |
| UBERON:0001765 | Mammary duct |
| UBERON:0000996 | Vagina |
| UBERON:0000002 | Uterine cervix |
| UBERON:0012249 | Ectocervix |
| UBERON:0001723 | Tongue |
| UBERON:0001828 | Gingiva |
| UBERON:0001831 | Parotid gland |
| UBERON:0003126 | Trachea |
| UBERON:0001255 | Urinary bladder |
| UBERON:0000989 | Penis |
| UBERON:0001013 | Adipose tissue |
- Ubiquitously expressed across most human tissues
- High expression in immune tissues (thymus, spleen, blood)
- High expression in epithelial tissues (skin, GI tract, lung)
- Significant expression in cardiovascular tissues
- Important in stem cell niches and developing tissues
Section 12: Disease Associations Mendelian/Monogenic Disease Links (GenCC)
| Disease | Classification | Inheritance | Source |
|---|---|---|---|
| Adams-Oliver syndrome 5 (OMIM:616028) | Definitive | Autosomal Dominant | LMM |
| Adams-Oliver syndrome 5 (OMIM:616028) | Strong | Autosomal Dominant | Labcorp |
| Adams-Oliver syndrome (MONDO:0007034) | Definitive | Autosomal Dominant | Illumina |
| Aortic valve disease 1 (OMIM:109730) | Strong | Autosomal Dominant | G2P |
| Leukodystrophy (MONDO:0019046) | Moderate | Autosomal Dominant | Ambry |
| Connective tissue disorder (MONDO:0003900) | Moderate | Autosomal Dominant | PanelApp |
| Familial bicuspid aortic valve (ORPHA:402075) | Supportive | Autosomal Dominant | Orphanet |
| Orphanet ID | Disease Name | Type | Gene Count |
|---|---|---|---|
| 974 | Adams-Oliver syndrome | Malformation syndrome | 6 |
| 402075 | Familial bicuspid aortic valve | Morphological anomaly | 5 |
| HPO ID | Phenotype |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0001647 | Bicuspid aortic valve |
| HP:0001650 | Aortic valve stenosis |
| HP:0001659 | Aortic regurgitation |
| HP:0001680 | Coarctation of aorta |
| HP:0001057 | Aplasia cutis congenita |
| HP:0001362 | Calvarial skull defect |
| HP:0001156 | Brachydactyly |
| HP:0001159 | Syndactyly |
| HP:0001171 | Split hand |
| HP:0004050 | Absent hand |
| HP:0010760 | Absent toe |
| HP:0001800 | Hypoplastic toenails |
| HP:0001802 | Absent toenail |
| HP:0001804 | Hypoplastic fingernail |
| HP:0001817 | Absent fingernail |
| HP:0001629 | Ventricular septal defect |
| HP:0001636 | Tetralogy of Fallot |
| HP:0001641 | Abnormal pulmonary valve morphology |
| HP:0001642 | Pulmonic stenosis |
| HP:0001655 | Patent foramen ovale |
| HP:0001667 | Right ventricular hypertrophy |
| HP:0001718 | Mitral stenosis |
| HP:0001719 | Double outlet right ventricle |
| HP:0002092 | Pulmonary arterial hypertension |
| HP:0004383 | Hypoplastic left ventricle |
| HP:0004935 | Pulmonary artery atresia |
| HP:0011560 | Mitral atresia |
| HP:0004380 | Aortic valve calcification |
| HP:0004933 | Ascending aortic dissection |
| HP:0004962 | Thoracic aorta calcification |
| HP:0005113 | Aortic arch aneurysm |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001269 | Hemiparesis |
| HP:0001276 | Hypertonia |
| HP:0002084 | Encephalocele |
| HP:0002132 | Porencephalic cyst |
| HP:0006970 | Periventricular leukomalacia |
| HP:0000238 | Hydrocephalus |
| HP:0001394 | Cirrhosis |
| HP:0001409 | Portal hypertension |
| HP:0001541 | Ascites |
| HP:0002612 | Congenital hepatic fibrosis |
| HP:0002040 | Esophageal varix |
| HP:0030242 | Portal vein thrombosis |
| HP:0001971 | Hypersplenism |
| HP:0001744 | Splenomegaly |
| HP:0001596 | Alopecia |
| HP:0008070 | Sparse hair |
| Study ID | Trait/Disease | P-value | Mapped Gene |
|---|---|---|---|
| GCST90002381 | Eosinophil count | 2.0e-21 | C9orf163-NOTCH1 |
| GCST90011900 | Serum alkaline phosphatase levels | 4.0e-19 | C9orf163-NOTCH1 |
| GCST004131 | Inflammatory bowel disease | 5.0e-36 | CARD9 region |
| GCST004132 | Crohn's disease | 6.0e-30 | CARD9 region |
| GCST004133 | Ulcerative colitis | 2.0e-16 | CARD9 region |
| GCST006804 | Red cell distribution width | 6.0e-09 | NOTCH1 |
| GCST010244 | Triglyceride levels | 6.0e-09 | C9orf163-NOTCH1 |
| GCST90002390 | Mean corpuscular hemoglobin | 7.0e-09 | NOTCH1 |
| GCST005537 | Chronic inflammatory diseases (pleiotropy) | 9.0e-09 | NOTCH1 |
| GCST003334 | Length of menstrual cycle | 2.0e-08 | NOTCH1 |
| GCST005173 | Coronary artery calcified plaque in T2D | 5.0e-06 | NOTCH1 |
T-cell acute lymphoblastic leukemia (T-ALL) - Activating mutations (~50% of cases)
Chronic lymphocytic leukemia (CLL) - Loss-of-function mutations
Head and neck squamous cell carcinoma (HNSCC) - Inactivating mutations
Cutaneous squamous cell carcinoma - Inactivating mutations
Adenoid cystic carcinoma - Activating mutations DATA SOURCES This reference document integrates data from:
HGNC (HUGO Gene Nomenclature Committee)
Ensembl (Release current)
NCBI Entrez Gene
OMIM (Online Mendelian Inheritance in Man)
UniProt (Swiss-Prot/TrEMBL)
PDB (Protein Data Bank)
AlphaFold
InterPro
Reactome
Gene Ontology
ClinVar
AlphaMissense
SpliceAI
STRING
IntAct
BioGRID
ChEMBL
PharmGKB
Bgee
GenCC
Orphanet
HPO (Human Phenotype Ontology)
GWAS Catalog
CollecTRI —Generated via biobtree cross-database mapping