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.

Datasets: 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, uniprot
Generated: 2026-03-27 — For the latest data, query BioBTree directly via MCP or API.
View API calls (40)
NOTCH1

Section 1: Gene Identifiers

DatabaseIdentifierNotes
HGNCHGNC:7881Approved symbol: NOTCH1
HGNC Namenotch receptor 1Status: Approved
Ensembl GeneENSG00000148400
NCBI Entrez Gene4851
OMIM190198Gene/Locus
Previous Symbols: TAN1 Previous Names: Notch (Drosophila) homolog 1 (translocation-associated); notch 1 Synonyms: AOS5, AOVD1, TAN1, hN1 Gene Groups: Notch receptors, MicroRNA protein coding host genes Genomic Location
AttributeValue
Chromosome9
Cytogenetic Band9q34.3
Start Position136,494,433
End Position136,546,048
StrandMinus (-)
Genome AssemblyGRCh38
Genomic AccessionNC_000009.12

Section 2: Transcript Identifiers Total Ensembl Transcripts: 17 Ensembl Transcripts (All)

Transcript IDBiotypeStartEnd
ENST00000651671protein_coding136,494,433136,546,048
ENST00000680218protein_coding136,494,433136,546,048
ENST00000680668protein_coding136,494,433136,546,048
ENST00000680133protein_coding136,494,457136,545,997
ENST00000927794protein_coding136,494,444136,545,851
ENST00000680778protein_coding136,494,433136,512,848
ENST00000679595nonsense_mediated_decay136,494,433136,546,048
ENST00000680924nonsense_mediated_decay136,494,444136,546,021
ENST00000681135nonsense_mediated_decay136,494,433136,546,048
ENST00000681454nonsense_mediated_decay136,494,433136,546,048
ENST00000491649retained_intron136,522,572136,523,898
ENST00000645828retained_intron136,502,437136,513,551
ENST00000646957retained_intron136,510,510136,513,110
ENST00000679969retained_intron136,494,444136,502,844
ENST00000680003retained_intron136,494,444136,502,695
ENST00000680882retained_intron136,508,293136,509,343
ENST00000681298retained_intron136,495,736136,508,369
RefSeq Transcripts
AccessionTypeStatusMANE Select
NM_017617mRNAREVIEWEDYES (Canonical)
NM_001105721mRNAPROVISIONALNo
XM_011518717mRNAPREDICTEDNo
XM_054363009mRNAPREDICTEDNo
RefSeq Proteins
AccessionStatusMANE Select
NP_060087REVIEWEDYES
NP_001099191PROVISIONALNo
XP_011517019PREDICTEDNo
XP_054218984PREDICTEDNo
CCDS
CCDS ID
CCDS43905
Canonical Transcript Exons (ENST00000651671) Total Exon Count: 34
Exon IDStartEndLength
ENSE00003850181136,545,726136,546,048322
ENSE00001124718136,544,024136,544,10278
ENSE00001042401136,523,717136,523,979262
ENSE00000985020136,522,850136,523,188338
ENSE00001378880136,519,443136,519,565122
ENSE00000985022136,518,591136,518,824233
ENSE00000985023136,518,137136,518,292155
ENSE00000985024136,517,752136,517,937185
ENSE00000985025136,517,272136,517,385113
ENSE00000985026136,515,981136,516,094113
ENSE00000985027136,515,483136,515,716233
ENSE00000985028136,515,290136,515,400110
ENSE00000985029136,514,510136,514,702192
ENSE00000985030136,513,392136,513,537145
ENSE00000985031136,513,021136,513,134113
ENSE00000985032136,511,152136,511,271119
ENSE00000985033136,510,653136,510,805152
ENSE00000985034136,509,733136,509,961228
ENSE00000985035136,508,870136,509,071201
ENSE00000985036136,508,232136,508,385153
ENSE00000985037136,507,955136,508,139184
ENSE00000985038136,507,305136,507,437132
ENSE00000985039136,506,716136,506,973257
ENSE00000985040136,506,527136,506,639112
ENSE00000985041136,505,310136,505,881571
ENSE00000985042136,504,673136,505,104431
ENSE00003681600136,503,182136,503,330148
ENSE00000985044136,502,272136,502,488216
ENSE00000985045136,502,001136,502,08887
ENSE00000985046136,501,748136,501,913165
ENSE00000985047136,500,552136,500,847295
ENSE00000985048136,499,112136,499,259147
ENSE00000985049136,498,899136,498,99697
ENSE00001247584136,494,433136,497,5583,125

Section 3: Protein Identifiers UniProt Accessions (Total: 9)

AccessionTypeNotes
P46531Reviewed (Swiss-Prot)CANONICAL
A0A7P0T8U6Unreviewed (TrEMBL)Isoform
A0A7P0T8W1Unreviewed (TrEMBL)Isoform
A0A7P0T9V1Unreviewed (TrEMBL)Isoform
A0A7P0TA56Unreviewed (TrEMBL)Isoform
A0A7P0TAK8Unreviewed (TrEMBL)Isoform
A0A7P0TB20Unreviewed (TrEMBL)Isoform
A0A7P0TBG2Unreviewed (TrEMBL)Isoform
A0A7P0Z4H9Unreviewed (TrEMBL)Isoform
Canonical Protein (P46531) Properties
PropertyValue
NameNeurogenic locus notch homolog protein 1
Alternative NameTranslocation-associated notch protein TAN-1
Length2,555 amino acids
Mass272,505 Da
Protein Domains and Families (InterPro) - Total: 17
InterPro IDNameType
IPR008297NotchFamily
IPR022362Notch_1Family
IPR051355Notch/Slit_guidanceFamily
IPR000742EGFDomain
IPR000800Notch_domDomain
IPR001881EGF-like_Ca-bd_domDomain
IPR010660Notch_NOD_domDomain
IPR011656Notch_NODP_domDomain
IPR024600Notch_CDomain
IPR049883NOTCH1_EGF-likeDomain
IPR002110Ankyrin_rptRepeat
IPR009030Growth_fac_rcpt_cys_sfHomologous superfamily
IPR035993Notch-like_dom_sfHomologous superfamily
IPR036770Ankyrin_rpt-contain_sfHomologous superfamily
IPR000152EGF-type_Asp/Asn_hydroxyl_sitePTM
IPR013032EGF-like_CSConserved site
IPR018097EGF_Ca-bd_CSConserved site

Section 4: Structure Identifiers Experimental Structures - Total PDB Count: 29

PDB IDMethodResolutionTitle
1PB5NMR-NMR Structure of a Prototype LNR Module from Human Notch1
1TOZNMR-NMR structure of the human NOTCH-1 ligand binding region
1YYHX-ray1.90 ÅCrystal structure of the human Notch 1 ankyrin domain
2F8XX-ray3.25 ÅCrystal structure of activated Notch, CSL and MAML on HES-1 promoter DNA
2F8YX-ray1.55 ÅCrystal structure of human Notch1 ankyrin repeats
2HE0X-ray1.90 ÅCrystal structure of a human Notch1 ankyrin domain mutant
2VJ3X-ray2.60 ÅHuman Notch-1 EGFs 11-13
3ETOX-ray2.00 Å2 Angstrom X-ray structure of the NOTCH1 Negative Regulatory Region
3I08X-ray3.20 ÅCrystal structure of the S1-cleaved Notch1 NRR
3L95X-ray2.19 ÅCrystal structure of human Notch1 NRR bound to antagonist antibody
3NBNX-ray3.45 ÅCrystal structure of a dimer of Notch Transcription Complex
3V79X-ray3.85 ÅStructure of human Notch1 transcription complex
4CUDX-ray1.85 ÅHuman Notch1 EGF domains 11-13 mutant fucosylated at T466
4CUEX-ray3.00 ÅHuman Notch1 EGF domains 11-13 mutant T466V
4CUFX-ray2.29 ÅHuman Notch1 EGF domains 11-13 mutant T466S
4D0EX-ray1.61 ÅHuman Notch1 EGF domains 11-13 with GlcNAc-fucose
4D0FX-ray2.80 ÅHuman Notch1 EGF domains 11-13 mutant T466A
5FM9X-ray2.92 ÅHuman Notch 1, EGF 4-7
5FMAX-ray2.46 ÅHuman Notch 1, EGF 4-7
5KZONMR-Notch1 transmembrane and juxtamembrane segment
5L0RX-ray1.50 ÅHuman POGLUT1 in complex with Notch1 EGF12
5UB5X-ray2.09 ÅHuman POGLUT1 in complex with human Notch1 EGF12 S458T mutant
6IDFCryo-EM2.70 ÅCryo-EM structure of gamma secretase in complex with Notch fragment
6PY8X-ray3.75 ÅCrystal structure of RBPJ-NOTCH1-NRARP ternary complex
8OR5NMR-Solution NMR structure of Notch1 TMD
8ORYNMR-Solution NMR structure of Notch1 L1740-1743 TMD
8ORZNMR-Solution NMR structure of Notch1 G1740-1743 TMD
9B3GX-ray1.55 ÅHuman Notch-1 EGFs 21-23
9B3NX-ray1.50 ÅHuman Notch-1 EGFs 20-24
Predicted Structures (AlphaFold)
Model IDSequence LengthGlobal pLDDTFraction Very High Confidence
P4653118,917 fragments59.740.03 (3%)

Section 5: Cross-Species Orthologs

OrganismGene IDSymbolBiotype
Mouse (Mus musculus)ENSMUSG00000026923Notch1protein_coding
Rat (Rattus norvegicus)ENSRNOG00000019322Notch1protein_coding
Zebrafish (Danio rerio)ENSDARG00000052094notch1bprotein_coding
Zebrafish (Danio rerio)ENSDARG00000103554notch1aprotein_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

ClassificationCount
Pathogenic85
Likely Pathogenic~100+
Uncertain Significance (VUS)~2,500+
Likely Benign~500+
Benign~200+
Conflicting Classifications~500+
TOP 50 Pathogenic Variants (ClinVar)
Variant IDHGVS NotationTypeReview Status
521568c.166C>T (p.Arg56Ter)SNVMultiple submitters
645087c.550C>T (p.Gln184Ter)SNVSingle submitter
221999c.578G>A (p.Gly193Asp)SNVNo assertion criteria
1428655c.428del (p.Pro143fs)DeletionMultiple submitters
523583c.415C>T (p.Gln139Ter)SNVSingle submitter
2123517c.410C>A (p.Ser137Ter)SNVSingle submitter
219375c.1343G>A (p.Arg448Gln)SNVSingle submitter
572044c.1396del (p.Thr466fs)DeletionSingle submitter
2636214c.1537C>T (p.Gln513Ter)SNVMultiple submitters
219378c.1649dup (p.Tyr550Ter)DupSingle submitter
3340288c.1650C>G (p.Tyr550Ter)SNVSingle submitter
1453811c.763_773del (p.Glu255fs)DeletionSingle submitter
523584c.794_797delinsCC (p.Asn265fs)IndelSingle submitter
845149c.1017_1018del (p.Ala340fs)DeletionSingle submitter
4293949c.873C>G (p.Tyr291Ter)SNVSingle submitter
1075050c.1784_1787del (p.Tyr595fs)DeletionSingle submitter
1409179c.1800_1801dup (p.Glu601fs)DupSingle submitter
3658668c.1847del (p.Gly616fs)DeletionSingle submitter
4635489c.1896del (p.Thr633fs)DeletionSingle submitter
3340287c.1904-2A>GSpliceSingle submitter
523585c.1935_1936del (p.Ala646fs)DeletionSingle submitter
4687945c.1987G>T (p.Glu663Ter)SNVSingle submitter
422753c.2023del (p.Cys675fs)DeletionSingle submitter
1344870c.2155G>T (p.Glu719Ter)SNVNo criteria
1344732c.2272G>T (p.Glu758Ter)SNVNo criteria
3235929c.2278_2282del (p.Asn760fs)DeletionSingle submitter
544178c.2365C>T (p.Gln789Ter)SNVMultiple submitters
523594c.2380G>T (p.Glu794Ter)SNVSingle submitter
3027324c.2407C>T (p.Gln803Ter)SNVSingle submitter
2633308c.2436del (p.Tyr813fs)DeletionSingle submitter
221998c.2439C>G (p.Tyr813Ter)SNVSingle submitter
817997c.2448dup (p.Cys817fs)DupMultiple submitters
2631128c.2536C>T (p.Gln846Ter)SNVSingle submitter
1961662c.2759dup (p.Ser921fs)DupSingle submitter
2695701c.2880C>A (p.Cys960Ter)SNVSingle submitter
520577c.3052del (p.Cys1018fs)DeletionSingle submitter
523596c.3281G>A (p.Cys1094Tyr)SNVSingle submitter
544179c.3266G>A (p.Trp1089Ter)SNVSingle submitter
4291131c.3316C>T (p.Gln1106Ter)SNVSingle submitter
12476c.3319C>T (p.Arg1107Ter)SNVMultiple submitters
3345218c.3332_3347del (p.Asp1111fs)DeletionSingle submitter
1344783c.3463C>T (p.Gln1155Ter)SNVNo criteria
3389911c.3656_3666del (p.Glu1219fs)DeletionSingle submitter
2671929c.3684del (p.Val1229fs)DeletionMultiple submitters
221997c.3765C>A (p.Cys1255Ter)SNVNo criteria
2843383c.3792_3793del (p.Cys1264_Glu1265delins*)DeletionSingle submitter
3880477c.3909_3919del (p.Cys1304fs)DeletionSingle submitter
2822065c.4021G>T (p.Glu1341Ter)SNVSingle submitter
566177c.4071C>A (p.Cys1357Ter)SNVSingle submitter
642523c.4127del (p.Gly1376fs)DeletionSingle submitter
AlphaMissense Predictions Total Missense Predictions: 16,909
ClassificationApproximate Count
Likely Pathogenic~4,000+
Ambiguous~3,000+
Likely Benign~9,000+
TOP 50 AlphaMissense Predicted Pathogenic Variants
VariantProtein ChangePathogenicity ScoreClass
9:136496143:C:AW2532C0.994likely_pathogenic
9:136496143:C:GW2532C0.994likely_pathogenic
9:136496179:C:AW2520C0.991likely_pathogenic
9:136496179:C:GW2520C0.991likely_pathogenic
9:136496181:A:GW2520R0.991likely_pathogenic
9:136496181:A:TW2520R0.991likely_pathogenic
9:136496145:A:GW2532R0.990likely_pathogenic
9:136496145:A:TW2532R0.990likely_pathogenic
9:136496125:G:CS2538R0.984likely_pathogenic
9:136496125:G:TS2538R0.984likely_pathogenic
9:136496173:G:CS2522R0.982likely_pathogenic
9:136496173:G:TS2522R0.982likely_pathogenic
9:136496212:G:CF2509L0.980likely_pathogenic
9:136496212:G:TF2509L0.980likely_pathogenic
9:136496213:A:CF2509C0.968likely_pathogenic
9:136496141:G:AS2533F0.937likely_pathogenic
9:136496148:C:GD2531H0.934likely_pathogenic
9:136496201:G:TS2513Y0.932likely_pathogenic
9:136496210:A:TL2510H0.928likely_pathogenic
9:136496147:A:CD2531V0.924likely_pathogenic
9:136496201:G:AS2513F0.921likely_pathogenic
9:136496213:A:GF2509S0.920likely_pathogenic
9:136496201:G:CS2513C0.916likely_pathogenic
9:136496142:A:GS2533P0.910likely_pathogenic
9:136496141:G:TS2533Y0.898likely_pathogenic
9:136496207:G:AT2511I0.896likely_pathogenic
9:136496180:C:AW2520L0.895likely_pathogenic
9:136496204:G:TP2512Q0.890likely_pathogenic
9:136496147:T:GD2531A0.890likely_pathogenic
9:136496141:G:CS2533C0.886likely_pathogenic
9:136496210:A:GL2510P0.886likely_pathogenic
9:136496148:C:AD2531Y0.885likely_pathogenic
9:136496177:G:AS2521F0.851likely_pathogenic
9:136496207:G:TT2511N0.851likely_pathogenic
9:136496147:T:CD2531G0.852likely_pathogenic
9:136496202:A:GS2513P0.842likely_pathogenic
9:136496198:G:TP2514H0.833likely_pathogenic
9:136496145:A:CW2520G0.799likely_pathogenic
9:136496204:G:AP2512L0.792likely_pathogenic
9:136496177:G:CS2521C0.791likely_pathogenic
9:136496138:T:AE2534V0.776likely_pathogenic
9:136496198:G:CP2514R0.764likely_pathogenic
9:136496208:T:CT2511A0.758likely_pathogenic
9:136496168:G:TS2524Y0.757likely_pathogenic
9:136496150:G:CS2530C0.752likely_pathogenic
9:136496174:C:TS2522N0.740likely_pathogenic
9:136496174:C:AS2522I0.739likely_pathogenic
9:136496199:G:AP2514S0.735likely_pathogenic
9:136496146:G:CD2531E0.733likely_pathogenic
9:136496168:G:AS2524F0.731likely_pathogenic
SpliceAI Predictions Total Splice Predictions: 5,610 TOP 50 SpliceAI Predicted Splice-Altering Variants
VariantEffectDelta Score
9:136497557:TCC:Tacceptor_loss1.000
9:136497560:T:Aacceptor_loss1.000
9:136497558:CCT:Cacceptor_loss1.000
9:136497554:TCCTC:Tacceptor_gain0.990
9:136497555:CCTCC:Cacceptor_gain0.990
9:136497556:CTC:Cacceptor_gain0.990
9:136497559:C:CCacceptor_gain0.990
9:136497557:TC:Tacceptor_gain0.980
9:136497558:CC:Cacceptor_gain0.980
9:136497566:A:ACacceptor_gain0.980
9:136497566:A:Cacceptor_gain0.980
9:136497905:T:TAdonor_gain0.950
9:136497555:CCTC:Cacceptor_gain0.930
9:136497557:TCCT:Tacceptor_gain0.930
9:136497556:CTCC:Cacceptor_gain0.930
9:136497558:C:Gacceptor_gain0.910
9:136497875:C:Adonor_gain0.820
9:136497559:C:Tacceptor_gain0.760
9:136497554:TCC:Tacceptor_gain0.750
9:136495700:T:Cacceptor_gain0.720
9:136497573:C:CTacceptor_gain0.680
9:136497538:C:CTacceptor_gain0.660
9:136495700:T:TCacceptor_gain0.650
9:136497922:G:Cdonor_gain0.630
9:136497527:TCCCG:Tacceptor_gain0.530
9:136497559:C:Gacceptor_gain0.530
9:136497561:G:Cacceptor_loss0.510
9:136497855:A:Tdonor_gain0.470
9:136497556:C:Tacceptor_gain0.460
9:136497528:C:Gacceptor_gain0.440
9:136497906:C:Adonor_gain0.440
9:136498278:TCTGC:Tdonor_gain0.440
9:136497574:G:Tacceptor_gain0.430
9:136497852:T:TAdonor_gain0.420
9:136497903:ATT:Adonor_gain0.420
9:136497560:T:TCacceptor_gain0.420
9:136497631:C:CTacceptor_gain0.420
9:136497918:CAGAG:Cdonor_gain0.410
9:136497986:C:CTdonor_gain0.400
9:136497928:G:Tdonor_gain0.380
9:136497874:T:TAdonor_gain0.380
9:136497530:C:CTacceptor_gain0.370
9:136497902:AATT:Adonor_gain0.370
9:136497719:AG:Adonor_gain0.360
9:136497480:G:Tacceptor_gain0.360
9:136497902:A:Tdonor_gain0.360
9:136497531:G:Tacceptor_gain0.350
9:136497901:AAATT:Adonor_gain0.340
9:136497860:A:ACdonor_gain0.340
9:136497861:C:CCdonor_gain0.340

Section 7: Biological Pathways & Gene Ontology Reactome Pathways - Total: 20

Pathway IDPathway NameDisease Pathway
R-HSA-1912399Pre-NOTCH Processing in the Endoplasmic ReticulumNo
R-HSA-1912408Pre-NOTCH Transcription and TranslationNo
R-HSA-1912420Pre-NOTCH Processing in GolgiNo
R-HSA-210744Regulation of gene expression in late stage pancreatic budNo
R-HSA-2122947NOTCH1 Intracellular Domain Regulates TranscriptionNo
R-HSA-2122948Activated NOTCH1 Transmits Signal to the NucleusNo
R-HSA-350054Notch-HLH transcription pathwayNo
R-HSA-8941856RUNX3 regulates NOTCH signalingNo
R-HSA-9013508NOTCH3 Intracellular Domain Regulates TranscriptionNo
R-HSA-9013695NOTCH4 Intracellular Domain Regulates TranscriptionNo
R-HSA-9793380Formation of paraxial mesodermNo
R-HSA-9818030NFE2L2 regulating tumorigenic genesNo
R-HSA-9818749Regulation of NFE2L2 gene expressionNo
R-HSA-9824272SomitogenesisNo
R-HSA-2644606Constitutive Signaling by NOTCH1 PEST Domain MutantsYes
R-HSA-2644607Loss of Function of FBXW7 in Cancer and NOTCH1 SignalingYes
R-HSA-2660826Constitutive Signaling by NOTCH1 t(7;9) Translocation MutantYes
R-HSA-2691232Constitutive Signaling by NOTCH1 HD Domain MutantsYes
R-HSA-2894862Constitutive Signaling by NOTCH1 HD+PEST Domain MutantsYes
R-HSA-5083630Defective LFNG causes SCDO3Yes
Gene Ontology Annotations - Total: 189 Biological Process (TOP 20 of ~140)
GO IDTerm Name
GO:0007219Notch signaling pathway
GO:0007221positive regulation of transcription of Notch receptor target
GO:0045747positive regulation of Notch signaling pathway
GO:0007507heart development
GO:0003180aortic valve morphogenesis
GO:0003181atrioventricular valve morphogenesis
GO:0003184pulmonary valve morphogenesis
GO:0003198epithelial to mesenchymal transition in endocardial cushion
GO:0060317cardiac epithelial to mesenchymal transition
GO:0001837epithelial to mesenchymal transition
GO:0002040sprouting angiogenesis
GO:0060842arterial endothelial cell differentiation
GO:0060843venous endothelial cell differentiation
GO:0045944positive regulation of transcription by RNA polymerase II
GO:0000122negative regulation of transcription by RNA polymerase II
GO:0048708astrocyte differentiation
GO:0048709oligodendrocyte differentiation
GO:0030216keratinocyte differentiation
GO:0035914skeletal muscle cell differentiation
GO:0008284positive regulation of cell population proliferation
Molecular Function (TOP 20 of ~12)
GO IDTerm Name
GO:0004888transmembrane signaling receptor activity
GO:0005112Notch binding
GO:0005509calcium ion binding
GO:0003713transcription coactivator activity
GO:0140537transcription regulator activator activity
GO:0031490chromatin DNA binding
GO:0019899enzyme binding
GO:0004857enzyme inhibitor activity
GO:0042802identical protein binding
Cellular Component (TOP 20 of ~25)
GO IDTerm Name
GO:0005886plasma membrane
GO:0016324apical plasma membrane
GO:0009986cell surface
GO:0005634nucleus
GO:0005654nucleoplasm
GO:0005829cytosol
GO:0005789endoplasmic reticulum membrane
GO:0000139Golgi membrane
GO:0010008endosome membrane
GO:0031902late endosome membrane
GO:0002193MAML1-RBP-Jkappa-ICN1 complex
GO:0043235receptor complex
GO:0005912adherens junction
GO:0005576extracellular region
GO:0098978glutamatergic synapse
GO:0098839postsynaptic density membrane
GO:0098685Schaffer collateral - CA1 synapse
GO:0001669acrosomal 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 IDScoreProtein Name
P46531999NOTCH1 (self)
Q06330999RBPJ (Recombining binding protein suppressor of hairless)
Q92585998MAML1 (Mastermind-like protein 1)
Q96JK9996MAML3
Q8IZL2995MAML2
O00548988DLL1 (Delta-like protein 1)
P78504988JAG1 (Jagged-1)
Q9NR61988DLL4 (Delta-like protein 4)
Q9Y219988JAG2 (Jagged-2)
Q9NYJ7987DLL3 (Delta-like protein 3)
Q15063970PSEN1 (Presenilin-1)
Q9BXP5960ADAM10
P84022943SMAD3
P35222932CTNNB1 (Beta-catenin)
Q16665918HIF1A
Q9Y6R0891NUMB
Q969H0885FBXW7
P49768884PSEN2 (Presenilin-2)
Q9Y5J3881TSPAN12
P00533873EGFR
Q5TA89872MFNG (Beta-1,3-N-acetylglucosaminyltransferase manic fringe)
Q9UBP5865HES5
Q86Y01850RFNG
P49757849NUMB-like protein
P19838809NFKB1
Q13485809SMAD4
P01106801MYC
P24385801CCND1 (Cyclin D1)
P25942799CD40
P04626787ERBB2
P04637787TP53
Q96T58775MFAP5
P48745766NOV (Nephroblastoma overexpressed gene protein)
P05067762APP
P31749757AKT1
P16070749CD44
P25490745TLE1
Q7Z6K4745LFNG
P09325741SFRP4
P60484737PTEN
P11362736FGFR1
Q96BI3727APH1A
Q14469725HES1
Q9UJU2725LEF1
P18443723RBX1
P49841723GSK3B
P28908721TNFRSF8
P48436717SOX9
Q8NES3713LFNG
P42336700PIK3CA
TOP 50 IntAct Interactions (by Confidence Score)
Interaction IDPartner GeneInteraction TypeScore
EBI-15698611MAML1physical association0.950
EBI-15814834MAML1association0.950
EBI-15886410MAML1physical association0.950
EBI-15886435MAML1direct interaction0.950
EBI-15968507MAML1physical association0.950
EBI-26972890MAML1physical association0.950
EBI-15621512RBPJassociation0.910
EBI-15662645FBXW7association0.880
EBI-15662673FBXW7direct interaction0.880
EBI-15876051FBXW7physical association0.880
EBI-16125085FBXW7physical association0.880
EBI-16125142FBXW7physical association0.880
EBI-16125197FBXW7physical association0.880
EBI-16125238FBXW7physical association0.880
EBI-16125275FBXW7physical association0.880
EBI-15814808RBPJassociation0.740
EBI-15814856RBPJdirect interaction0.740
EBI-15814877RBPJdirect interaction0.740
EBI-15968483RBPJdirect interaction0.740
EBI-15968534RBPJdirect interaction0.740
EBI-15968557RBPJdirect interaction0.740
EBI-15718282JAG1direct interaction0.730
EBI-15718305JAG1direct interaction0.730
EBI-15718326JAG1direct interaction0.730
EBI-15718354JAG1direct interaction0.730
EBI-16154871ATMphysical association0.660
EBI-16154888ATMphysical association0.660
EBI-16154928ATMphysical association0.660
EBI-16154945ATMphysical association0.660
EBI-16154988ATMdirect interaction0.660
EBI-13916003KDM1Aassociation0.560
EBI-13916171KDM1Aassociation0.560
EBI-13916205KDM1Aphysical association0.560
EBI-13916240KDM1Aassociation0.560
EBI-13916258KDM1Aassociation0.560
EBI-13916271KDM1Aassociation0.560
EBI-13916303KDM1Aassociation0.560
EBI-26972899MAML3physical association0.550
EBI-15698630HIF1Aphysical association0.500
EBI-15698649HIF1Aassociation0.500
EBI-13916178PHF8association0.460
EBI-13916185SMARCA4association0.460
EBI-13916287SMARCA4association0.460
EBI-13916322MAPK1association0.460
EBI-13916342RBBP4association0.460
EBI-13916352PRKDCassociation0.460
EBI-11473706HIF1ANhydroxylation reaction0.440
EBI-11510948LILRB2physical association0.400
EBI-21398082NOTCH1physical association (homo)0.400
EBI-27039608ABL1physical association0.370
Protein Similarity ESM2 Structural/Embedding Similarity - Total: 25 Similar Proteins
UniProt IDTop SimilarityAvg SimilarityProtein
Q017050.99980.9785NOTCH2 (Human)
Q070080.99980.9785NOTCH3 (Human)
O355160.99980.9792Notch1 (Mouse)
Q9QW300.99980.9795Notch1 (Mouse)
Q619820.99970.9735Notch2 (Mouse)
R91720.99970.9727Notch3 (Mouse)
A2RUV00.99960.9758Notch1 (Zebrafish)
P217830.99960.9758Notch (Drosophila)
Q5ZQU00.99990.9829Notch1 (Chicken)
Q70E200.99990.9829Notch1 (Chicken)
Q047210.99940.9793Notch2
G3I6Z60.99930.9794Notch1
A0A096LNW50.99860.9797Notch1 isoform
P0DPK30.99860.9798Notch1 isoform
Q9UM470.99860.9689NOTCH4 (Human)
Q8TER00.99840.9818Notch1
Q316950.99800.9687Notch
Q994660.99800.9632NOTCH4
P465300.99650.9773NOTCH2
Q7Z3S90.99560.9796NOTCH3
Diamond Sequence Similarity - Total: 67 Homologous Proteins
UniProt IDTop Identity %Protein
B4DH59100.0NOTCH1 isoform
A0A096LNW5100.0NOTCH1 isoform
P0DPK3100.0NOTCH1 isoform
Q0170598.9NOTCH2 (Human)
Q0700898.9NOTCH3 (Human)
G3I6Z697.5Notch1
O3551696.3Notch1 (Mouse)
Q9QW3096.3Notch1 (Mouse)
Q6RI8696.8Notch1
Q6198294.9Notch2 (Mouse)
Q9P2R394.9NOTCH4
Q810B694.9Notch1
A2VCU893.7Notch1
Q7ZXL593.7Notch1
Q9283293.6Notch2
A2RUV092.2Notch1
P2178392.2Notch (Drosophila)
Q9UM4791.0NOTCH4 (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 GeneRegulationConfidence
BCL11BActivationHigh
CTNNB1ActivationHigh
GATA5ActivationLow
KLF5ActivationLow
LEF1Activation-
MAML1Activation-
MAML2Activation-
BMP2Activation-
CD46Activation-
CGAActivation-
FSHBActivation-
FOXO3Repression-
IKZF1RepressionLow
MECP2Repression-
MESP2Repression-
AHRUnknownHigh
AP1UnknownHigh
ARUnknownHigh
CEBPBUnknownHigh
CEBPDUnknownHigh
CREB1UnknownHigh
CREMUnknownHigh
CRXUnknownHigh
CTBP2UnknownHigh
DLX4UnknownHigh
EGR1UnknownHigh
ESR1UnknownHigh
ESR2UnknownHigh
ETS2UnknownHigh
ETV4UnknownHigh
EZH2UnknownHigh
FOSUnknownHigh
FOXA2UnknownHigh
FOXN1UnknownHigh
FOXO1UnknownHigh
GATA4UnknownHigh
GLI3UnknownHigh
GRHL3UnknownHigh
HES1UnknownHigh
HES5UnknownHigh
HIF1AUnknownHigh
ID2UnknownHigh
ID3UnknownHigh
IRF1UnknownHigh
ISL1UnknownHigh
JARID2UnknownHigh
JUNUnknownHigh
JUNBUnknownHigh
JUNDUnknownHigh
KAT7UnknownHigh
Downstream Targets - NOTCH1 as Transcriptional Regulator NOTCH1 intracellular domain (NICD) forms a complex with RBPJ and MAML proteins to regulate transcription of target genes including:
  • 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 IDTarget NameType
CHEMBL2146346Neurogenic locus notch homolog protein 1SINGLE PROTEIN
CHEMBL4524007Notch receptorPROTEIN FAMILY
Targeting Molecules Total Compounds with Activity Data: 100+
ChEMBL IDNameTypeHighest Phase
CHEMBL3911164VAREGACESTATSmall moleculePhase 2
CHEMBL360322-Small moleculePhase 0
CHEMBL3604460-Small moleculePhase 0
CHEMBL3890931-Small moleculePhase 0
CHEMBL3891599-Small moleculePhase 0
CHEMBL3893305-Small moleculePhase 0
(100+ additional compounds in preclinical)-Small moleculePhase 0
Note: Most NOTCH1-targeting compounds are gamma-secretase inhibitors that prevent NOTCH1 cleavage and activation. PharmGKB Information
AttributeValue
PharmGKB IDPA31683
SymbolNOTCH1
VIP GeneYes
CPIC GuidelineNo
Chromosomechr9
Drug-Gene Interactions NOTCH1 is involved in resistance mechanisms to various cancer therapies including:
  • Glucocorticoids (in T-ALL)
  • CDK4/6 inhibitors
  • PI3K inhibitors

Section 11: Expression Profiles Bgee Expression Summary

PropertyValue
Expression BreadthUbiquitous
Total Present Calls272
Max Expression Score97.85
TOP 30 Tissues with NOTCH1 Expression (Bgee/UBERON)
Tissue (UBERON)Tissue Name
UBERON:0000178Blood
UBERON:0002370Thymus
UBERON:0002106Spleen
UBERON:0002372Tonsil
UBERON:0002048Lung
UBERON:0008949Lower lobe of lung
UBERON:0008948Upper lobe of lung
UBERON:0001043Esophagus
UBERON:0002469Esophagus mucosa
UBERON:0001160Fundus of stomach
UBERON:0001199Mucosa of stomach
UBERON:0001155Colon
UBERON:0000317Colonic mucosa
UBERON:0001157Transverse colon
UBERON:0000160Intestine
UBERON:0000059Large intestine
UBERON:0001153Caecum
UBERON:0002098Apex of heart
UBERON:0001911Mammary gland
UBERON:0001765Mammary duct
UBERON:0000996Vagina
UBERON:0000002Uterine cervix
UBERON:0012249Ectocervix
UBERON:0001723Tongue
UBERON:0001828Gingiva
UBERON:0001831Parotid gland
UBERON:0003126Trachea
UBERON:0001255Urinary bladder
UBERON:0000989Penis
UBERON:0001013Adipose tissue
Expression Pattern Notes
  • 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)

DiseaseClassificationInheritanceSource
Adams-Oliver syndrome 5 (OMIM:616028)DefinitiveAutosomal DominantLMM
Adams-Oliver syndrome 5 (OMIM:616028)StrongAutosomal DominantLabcorp
Adams-Oliver syndrome (MONDO:0007034)DefinitiveAutosomal DominantIllumina
Aortic valve disease 1 (OMIM:109730)StrongAutosomal DominantG2P
Leukodystrophy (MONDO:0019046)ModerateAutosomal DominantAmbry
Connective tissue disorder (MONDO:0003900)ModerateAutosomal DominantPanelApp
Familial bicuspid aortic valve (ORPHA:402075)SupportiveAutosomal DominantOrphanet
Orphanet Disease Associations
Orphanet IDDisease NameTypeGene Count
974Adams-Oliver syndromeMalformation syndrome6
402075Familial bicuspid aortic valveMorphological anomaly5
HPO Phenotype Associations - Total: 79
HPO IDPhenotype
HP:0000006Autosomal dominant inheritance
HP:0001647Bicuspid aortic valve
HP:0001650Aortic valve stenosis
HP:0001659Aortic regurgitation
HP:0001680Coarctation of aorta
HP:0001057Aplasia cutis congenita
HP:0001362Calvarial skull defect
HP:0001156Brachydactyly
HP:0001159Syndactyly
HP:0001171Split hand
HP:0004050Absent hand
HP:0010760Absent toe
HP:0001800Hypoplastic toenails
HP:0001802Absent toenail
HP:0001804Hypoplastic fingernail
HP:0001817Absent fingernail
HP:0001629Ventricular septal defect
HP:0001636Tetralogy of Fallot
HP:0001641Abnormal pulmonary valve morphology
HP:0001642Pulmonic stenosis
HP:0001655Patent foramen ovale
HP:0001667Right ventricular hypertrophy
HP:0001718Mitral stenosis
HP:0001719Double outlet right ventricle
HP:0002092Pulmonary arterial hypertension
HP:0004383Hypoplastic left ventricle
HP:0004935Pulmonary artery atresia
HP:0011560Mitral atresia
HP:0004380Aortic valve calcification
HP:0004933Ascending aortic dissection
HP:0004962Thoracic aorta calcification
HP:0005113Aortic arch aneurysm
HP:0001249Intellectual disability
HP:0001250Seizure
HP:0001269Hemiparesis
HP:0001276Hypertonia
HP:0002084Encephalocele
HP:0002132Porencephalic cyst
HP:0006970Periventricular leukomalacia
HP:0000238Hydrocephalus
HP:0001394Cirrhosis
HP:0001409Portal hypertension
HP:0001541Ascites
HP:0002612Congenital hepatic fibrosis
HP:0002040Esophageal varix
HP:0030242Portal vein thrombosis
HP:0001971Hypersplenism
HP:0001744Splenomegaly
HP:0001596Alopecia
HP:0008070Sparse hair
GWAS Associations - Total: 11
Study IDTrait/DiseaseP-valueMapped Gene
GCST90002381Eosinophil count2.0e-21C9orf163-NOTCH1
GCST90011900Serum alkaline phosphatase levels4.0e-19C9orf163-NOTCH1
GCST004131Inflammatory bowel disease5.0e-36CARD9 region
GCST004132Crohn's disease6.0e-30CARD9 region
GCST004133Ulcerative colitis2.0e-16CARD9 region
GCST006804Red cell distribution width6.0e-09NOTCH1
GCST010244Triglyceride levels6.0e-09C9orf163-NOTCH1
GCST90002390Mean corpuscular hemoglobin7.0e-09NOTCH1
GCST005537Chronic inflammatory diseases (pleiotropy)9.0e-09NOTCH1
GCST003334Length of menstrual cycle2.0e-08NOTCH1
GCST005173Coronary artery calcified plaque in T2D5.0e-06NOTCH1
Cancer Associations NOTCH1 is recurrently mutated in:
  • 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