Gene Gene information from NCBI Gene database.
Entrez ID 83882
Gene name Tetraspanin 10
Gene symbol TSPAN10
Synonyms (NCBI Gene)
OCSP
Chromosome 17
Chromosome location 17q25.3
miRNA miRNA information provided by mirtarbase database.
12
miRTarBase ID miRNA Experiments Reference
MIRT574049 hsa-miR-6869-3p PAR-CLIP 20371350
MIRT574048 hsa-miR-3960 PAR-CLIP 20371350
MIRT574047 hsa-miR-8072 PAR-CLIP 20371350
MIRT574046 hsa-miR-4467 PAR-CLIP 20371350
MIRT574048 hsa-miR-3960 PAR-CLIP 26701625
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28514442, 33961781
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0019899 Function Enzyme binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H1Z9
Protein name Tetraspanin-10 (Tspan-10) (Oculospanin)
Protein function Part of TspanC8 subgroup, composed of 6 members that interact with the transmembrane metalloprotease ADAM10. This interaction is required for ADAM10 exit from the endoplasmic reticulum and for enzymatic maturation and trafficking to the cell sur
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00335 Tetraspanin 76 318 Tetraspanin family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the eye, including iris, ciliary body, retinal pigment epithelium, but not lens (protein level). {ECO:0000269|PubMed:12107410}.
Sequence
Sequence length 355
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
CORNEAL ASTIGMATISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EYE DISEASE 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
Alzheimer Disease Alzheimer disease Pubtator 30535121, 36951251 Associate
★☆☆☆☆
Found in Text Mining only
Astigmatism Astigmatism Pubtator 30306274 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 33960436 Associate
★☆☆☆☆
Found in Text Mining only
Cerebrovascular accident Stroke BEFREE 15001788
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 30535121 Associate
★☆☆☆☆
Found in Text Mining only
Hereditary Breast and Ovarian Cancer Syndrome Hereditary breast and ovarian cancer syndrome Pubtator 30535121 Associate
★☆☆☆☆
Found in Text Mining only
Ischemic stroke Ischemic Stroke BEFREE 24727681
★☆☆☆☆
Found in Text Mining only
Macular Degeneration Macular degeneration Pubtator 31995762 Associate
★☆☆☆☆
Found in Text Mining only
Myocardial Infarction Myocardial Infarction BEFREE 15001788
★☆☆☆☆
Found in Text Mining only
Myopia Myopia GWASCAT_DG 27182965
★☆☆☆☆
Found in Text Mining only