GBA Gene Complete Identifier and Functional Mapping Reference
Provide a comprehensive cross-database identifier and functional mapping reference for human GBA. This should serve as a definitive lookup resource …
Provide a comprehensive cross-database identifier and functional mapping reference for human GBA. 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 34 biological databases.
Further analyze this answer or run your own queries with BioBTree MCP.
alphafold, alphamissense, bgee, biogrid_interaction, 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, pfam, pharmgkb_gene, reactome, refseq, signor, spliceai, string_interaction, transcript, uniprotView API calls (44)
- search(GBA) https://sugi.bio/biobtree/api/search?i=GBA
- entry(HGNC:4177, hgnc) https://sugi.bio/biobtree/api/entry?i=HGNC%3A4177&s=hgnc
- map(HGNC:4177, >>hgnc>>ensembl) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eensembl
- map(HGNC:4177, >>hgnc>>entrez) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eentrez
- map(HGNC:4177, >>hgnc>>mim) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Emim
- map(HGNC:4177, >>hgnc>>uniprot) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Euniprot
- entry(ENSG00000177628, ensembl) https://sugi.bio/biobtree/api/entry?i=ENSG00000177628&s=ensembl
- entry(P04062, uniprot) https://sugi.bio/biobtree/api/entry?i=P04062&s=uniprot
- map(ENSG00000177628, >>ensembl>>transcript) https://sugi.bio/biobtree/api/map?i=ENSG00000177628&m=%3E%3Eensembl%3E%3Etranscript
- map(ENSG00000177628, >>ensembl>>ortholog) https://sugi.bio/biobtree/api/map?i=ENSG00000177628&m=%3E%3Eensembl%3E%3Eortholog
- map(HGNC:4177, >>hgnc>>refseq) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Erefseq
- map(HGNC:4177, >>hgnc>>ccds) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eccds
- map(P04062, >>uniprot>>interpro) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Einterpro
- map(P04062, >>uniprot>>pdb) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Epdb
- map(P04062, >>uniprot>>alphafold) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ealphafold
- map(P04062, >>uniprot>>pfam) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Epfam
- map(ENST00000327247, >>transcript>>exon) https://sugi.bio/biobtree/api/map?i=ENST00000327247&m=%3E%3Etranscript%3E%3Eexon
- map(HGNC:4177, >>hgnc>>clinvar) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eclinvar
- map(P04062, >>uniprot>>go) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ego
- map(P04062, >>uniprot>>reactome) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ereactome
- map(P04062, >>uniprot>>string_interaction) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Estring_interaction
- map(HGNC:4177, >>hgnc>>clinvar) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eclinvar
- map(HGNC:4177, >>hgnc>>spliceai) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Espliceai
- map(P04062, >>uniprot>>alphamissense) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ealphamissense
- map(HGNC:4177, >>hgnc>>hpo) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Ehpo
- map(HGNC:4177, >>hgnc>>gencc) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Egencc
- map(P04062, >>uniprot>>esm2_similarity) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Eesm2_similarity
- map(P04062, >>uniprot>>diamond_similarity) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ediamond_similarity
- map(P04062, >>uniprot>>chembl_target) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Echembl_target
- map(HGNC:4177, >>hgnc>>pharmgkb_gene) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Epharmgkb_gene
- map(P04062, >>uniprot>>intact) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Eintact
- map(P04062, >>uniprot>>signor) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Esignor
- map(CHEMBL2179, >>chembl_target>>chembl_molecule) https://sugi.bio/biobtree/api/map?i=CHEMBL2179&m=%3E%3Echembl_target%3E%3Echembl_molecule
- map(ENSG00000177628, >>ensembl>>bgee) https://sugi.bio/biobtree/api/map?i=ENSG00000177628&m=%3E%3Eensembl%3E%3Ebgee
- map(HGNC:4177, >>hgnc>>gwas) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Egwas
- map(HGNC:4177, >>hgnc>>orphanet) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eorphanet
- map(HGNC:4177, >>hgnc>>mim) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Emim
- entry(ENSG00000177628, bgee) https://sugi.bio/biobtree/api/entry?i=ENSG00000177628&s=bgee
- map(CHEMBL2179, >>chembl_target>>chembl_molecule[highestDevelopmentPhase>=3]) https://sugi.bio/biobtree/api/map?i=CHEMBL2179&m=%3E%3Echembl_target%3E%3Echembl_molecule%5BhighestDevelopmentPhase%3E%3D3%5D
- map(HGNC:4177, >>hgnc>>collectri) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Ecollectri
- map(HGNC:4177, >>hgnc>>clinvar[germline_classification=="Pathogenic"]) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Eclinvar%5Bgermline_classification%3D%3D%22Pathogenic%22%5D
- map(P04062, >>uniprot>>biogrid_interaction) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ebiogrid_interaction
- map(HGNC:4177, >>hgnc>>hpo) https://sugi.bio/biobtree/api/map?i=HGNC%3A4177&m=%3E%3Ehgnc%3E%3Ehpo
- map(P04062, >>uniprot>>alphamissense[am_class=="likely_pathogenic"]) https://sugi.bio/biobtree/api/map?i=P04062&m=%3E%3Euniprot%3E%3Ealphamissense%5Bam_class%3D%3D%22likely_pathogenic%22%5D
| Database | Identifier | Notes |
|---|---|---|
| HGNC ID | HGNC:4177 | Approved |
| Approved Symbol | GBA1 | |
| Previous Symbols | GBA, GLUC | |
| Approved Name | glucosylceramidase beta 1 | |
| Ensembl Gene | ENSG00000177628 | |
| NCBI Entrez Gene | 2629 | |
| OMIM Gene/Locus | 606463 | |
| Locus Group | protein-coding gene |
| Attribute | Value |
|---|---|
| Chromosome | 1 |
| Cytogenetic Band | 1q22 |
| Start Position | 155,234,447 |
| End Position | 155,245,178 |
| Strand | Minus (-) |
| Gene Span | 10,731 bp |
Section 2: Transcript Identifiers Ensembl Transcripts Total Transcripts: 27
| Transcript ID | Biotype | Start | End | Notes |
|---|---|---|---|---|
| ENST00000327247 | protein_coding | 155,234,452 | 155,244,670 | Canonical |
| ENST00000368373 | protein_coding | 155,234,452 | 155,241,249 | |
| ENST00000427500 | protein_coding | 155,234,559 | 155,241,275 | |
| ENST00000428024 | protein_coding | 155,234,868 | 155,244,699 | |
| ENST00000852359 | protein_coding | 155,234,453 | 155,245,178 | |
| ENST00000852360 | protein_coding | 155,234,447 | 155,244,699 | |
| ENST00000852361 | protein_coding | 155,234,453 | 155,244,690 | |
| ENST00000852362 | protein_coding | 155,234,449 | 155,244,678 | |
| ENST00000852363 | protein_coding | 155,234,452 | 155,244,677 | |
| ENST00000852364 | protein_coding | 155,234,453 | 155,244,673 | |
| ENST00000852365 | protein_coding | 155,234,453 | 155,244,665 | |
| ENST00000852366 | protein_coding | 155,234,452 | 155,244,379 | |
| ENST00000852367 | protein_coding | 155,234,452 | 155,241,226 | |
| ENST00000852368 | protein_coding | 155,234,933 | 155,241,262 | |
| ENST00000948996 | protein_coding | 155,234,453 | 155,244,673 | |
| ENST00000948997 | protein_coding | 155,234,453 | 155,244,629 | |
| ENST00000948998 | protein_coding | 155,234,453 | 155,241,263 | |
| ENST00000460156 | protein_coding_CDS_not_defined | 155,237,932 | 155,238,891 | |
| ENST00000464536 | protein_coding_CDS_not_defined | 155,234,453 | 155,235,835 | |
| ENST00000467918 | protein_coding_CDS_not_defined | 155,239,635 | 155,244,606 | |
| ENST00000470104 | protein_coding_CDS_not_defined | 155,239,960 | 155,241,243 | |
| ENST00000473570 | protein_coding_CDS_not_defined | 155,238,564 | 155,244,622 | |
| ENST00000478472 | protein_coding_CDS_not_defined | 155,234,961 | 155,236,459 | |
| ENST00000484489 | protein_coding_CDS_not_defined | 155,235,016 | 155,241,231 | |
| ENST00000491081 | protein_coding_CDS_not_defined | 155,236,182 | 155,238,709 | |
| ENST00000493842 | protein_coding_CDS_not_defined | 155,238,213 | 155,244,636 | |
| ENST00000497670 | protein_coding_CDS_not_defined | 155,236,396 | 155,239,962 |
| RefSeq ID | Type | Status | MANE Select |
|---|---|---|---|
| NM_000157 | mRNA | REVIEWED | ✓ YES |
| NM_001005741 | mRNA | REVIEWED | No |
| NM_001005742 | mRNA | REVIEWED | No |
| NM_001171811 | mRNA | REVIEWED | No |
| NM_001171812 | mRNA | REVIEWED | No |
| RefSeq ID | Type | Status | MANE Select |
|---|---|---|---|
| NP_000148 | protein | REVIEWED | ✓ YES |
| NP_001005741 | protein | REVIEWED | No |
| NP_001005742 | protein | REVIEWED | No |
| NP_001165282 | protein | REVIEWED | No |
| NP_001165283 | protein | REVIEWED | No |
Document generated from BioBTree cross-database queries. Data current as of query date. I have compiled a comprehensive cross-database identifier and functional mapping reference for human GBA1 (GBA) gene. This document includes: Key highlights:
58 PDB crystal structures (best resolution: 0.98Å)
538 ClinVar variants including 73 pathogenic
3,497 AlphaMissense predictions for missense pathogenicity
1,337 SpliceAI predictions for splice effects
2,346+ STRING protein interactions
251 HPO phenotype terms associated with GBA1 mutations
8 approved/Phase 3+ drug molecules targeting GBA1 Clinical significance:
GBA1 mutations cause Gaucher disease (types I, II, III, perinatal lethal) - autosomal recessive
GBA1 variants are the strongest genetic risk factor for Parkinson’s disease - autosomal dominant risk
The gene encodes lysosomal acid glucosylceramidase, essential for sphingolipid metabolism
Ubiquitously expressed with highest levels in endometrial stromal cells, pancreatic islets, placenta, and blood cells