Gene Gene information from NCBI Gene database.
Entrez ID 55973
Gene name B cell receptor associated protein 29
Gene symbol BCAP29
Synonyms (NCBI Gene)
B29BAP29
Chromosome 7
Chromosome location 7q22.3
miRNA miRNA information provided by mirtarbase database.
510
miRTarBase ID miRNA Experiments Reference
MIRT022570 hsa-miR-124-3p Microarray 18668037
MIRT023730 hsa-miR-1-3p Microarray 18668037
MIRT050398 hsa-miR-23a-3p CLASH 23622248
MIRT817315 hsa-let-7a CLIP-seq
MIRT817316 hsa-let-7b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0001649 Process Osteoblast differentiation HDA 16210410
GO:0005515 Function Protein binding IPI 28514442, 30021884, 33961781, 35271311
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IBA
GO:0005789 Component Endoplasmic reticulum membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619612 24131 ENSG00000075790
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UHQ4
Protein name B-cell receptor-associated protein 29 (BCR-associated protein 29) (Bap29)
Protein function May play a role in anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi. May be involved in CASP8-mediated apoptosis (By similarity).
PDB 4W7Y , 4W7Z , 4W80
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05529 Bap31 1 137 Bap31/Bap29 transmembrane region Family
PF18035 Bap31_Bap29_C 182 241 Bap31/Bap29 cytoplasmic coiled-coil domain Coiled-coil
Sequence
Sequence length 241
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autistic Disorder Autism Pubtator 37794117 Associate
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Coronary artery disease GWASCAT_DG 29212778
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Coronary heart disease Coronary Heart Disease GWASDB_DG 21378988
★☆☆☆☆
Found in Text Mining only
Coronary heart disease Coronary Heart Disease GWASCAT_DG 21378988
★☆☆☆☆
Found in Text Mining only
Degenerative polyarthritis Arthritis BEFREE 22586168
★☆☆☆☆
Found in Text Mining only
Myocardial Infarction Myocardial infarction Pubtator 24475106 Associate
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia Pubtator 37794117 Associate
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 28415823 Associate
★☆☆☆☆
Found in Text Mining only