Gene Gene information from NCBI Gene database.
Entrez ID 11199
Gene name Annexin A10
Gene symbol ANXA10
Synonyms (NCBI Gene)
ANX14
Chromosome 4
Chromosome location 4q32.3
Summary This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. The function of this gene has not yet been dete
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0001786 Function Phosphatidylserine binding IBA
GO:0005509 Function Calcium ion binding IEA
GO:0005509 Function Calcium ion binding TAS 10458909
GO:0005515 Function Protein binding IPI 21516116, 25416956, 29892012, 31515488, 32296183
GO:0005544 Function Calcium-dependent phospholipid binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608008 534 ENSG00000109511
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UJ72
Protein name Annexin A10 (Annexin-10) (Annexin-14)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00191 Annexin 21 86 Annexin Family
PF00191 Annexin 93 158 Annexin Family
PF00191 Annexin 175 241 Annexin Family
PF00191 Annexin 251 316 Annexin Family
Sequence
Sequence length 324
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANDROGENETIC ALOPECIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL LEFT-SIDED HEART LESIONS 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
Adenocarcinoma Adenocarcinoma BEFREE 22901464, 28369074, 29507659
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma Of Esophagus Esophageal Cancer BEFREE 18219111
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of pancreas Pancreatic adenocarcinoma BEFREE 28369074
★☆☆☆☆
Found in Text Mining only
Adenoma Adenoma BEFREE 24909058, 25395067, 31211760
★☆☆☆☆
Found in Text Mining only
Adenomatous Polyposis Coli Multiple polyposis syndrome BEFREE 31211760
★☆☆☆☆
Found in Text Mining only
Anodontia Anodontia Pubtator 32583331 Associate
★☆☆☆☆
Found in Text Mining only
ANOPHTHALMIA AND PULMONARY HYPOPLASIA Syndromic microphthalmia BEFREE 28369074
★☆☆☆☆
Found in Text Mining only
Barrett Esophagus Barrett esophagus BEFREE 18430189
★☆☆☆☆
Found in Text Mining only
Bladder Neoplasm Bladder Neoplasm BEFREE 30553612
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 12000734, 19582876, 21175800, 24909058, 27862098
★☆☆☆☆
Found in Text Mining only