Gene Gene information from NCBI Gene database.
Entrez ID 56344
Gene name Calcium binding protein 5
Gene symbol CABP5
Synonyms (NCBI Gene)
CABP3
Chromosome 19
Chromosome location 19q13.33
Summary The product of this gene belongs to a subfamily of calcium binding proteins, which share similarity to calmodulin. Calcium binding proteins are an important component of calcium mediated cellular signal transduction. Expression of this gene is retina-spec
miRNA miRNA information provided by mirtarbase database.
59
miRTarBase ID miRNA Experiments Reference
MIRT017682 hsa-miR-335-5p Microarray 18185580
MIRT857306 hsa-miR-1275 CLIP-seq
MIRT857307 hsa-miR-1470 CLIP-seq
MIRT857308 hsa-miR-184 CLIP-seq
MIRT857309 hsa-miR-219-1-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005246 Function Calcium channel regulator activity IBA
GO:0005509 Function Calcium ion binding IEA
GO:0005509 Function Calcium ion binding NAS 10625670
GO:0005515 Function Protein binding IPI 25416956, 29892012, 31515488, 32296183, 33961781
GO:0005737 Component Cytoplasm IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607315 13714 ENSG00000105507
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NP86
Protein name Calcium-binding protein 5 (CaBP5)
Protein function Inhibits calcium-dependent inactivation of L-type calcium channel and shifts voltage dependence of activation to more depolarized membrane potentials (By similarity). Involved in the transmission of light signals (By similarity). May positively
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13499 EF-hand_7 30 94 EF-hand domain pair Domain
PF13499 EF-hand_7 107 172 EF-hand domain pair Domain
Tissue specificity TISSUE SPECIFICITY: Retina. {ECO:0000269|PubMed:11108966}.
Sequence
Sequence length 173
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations