Gene Gene information from NCBI Gene database.
Entrez ID 10100
Gene name Tetraspanin 2
Gene symbol TSPAN2
Synonyms (NCBI Gene)
NET3TSN2TSPAN-2
Chromosome 1
Chromosome location 1p13.2
Summary The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate
miRNA miRNA information provided by mirtarbase database.
231
miRTarBase ID miRNA Experiments Reference
MIRT520451 hsa-miR-6074 HITS-CLIP 19536157
MIRT520450 hsa-miR-664a-3p HITS-CLIP 19536157
MIRT520445 hsa-miR-452-3p HITS-CLIP 19536157
MIRT509193 hsa-miR-8485 HITS-CLIP 19536157
MIRT509192 hsa-miR-329-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25814554, 32296183, 32814053
GO:0005654 Component Nucleoplasm IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0006954 Process Inflammatory response IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613133 20659 ENSG00000134198
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60636
Protein name Tetraspanin-2 (Tspan-2) (Tetraspan NET-3)
Protein function May play a role in signalling in oligodendrocytes in the early stages of their terminal differentiation into myelin-forming glia and may also function in stabilizing the mature sheath.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00335 Tetraspanin 11 213 Tetraspanin family Family
Sequence
Sequence length 221
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs9659602 RCV005910616
Colon adenocarcinoma Benign rs9659602 RCV005910615
Lung cancer Benign rs9659602 RCV005910620
Ovarian serous cystadenocarcinoma Benign rs9659602 RCV005910618
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arteriovenous Fistula Associate 28258189
Atherosclerosis Associate 26708676
Bipolar Disorder Associate 36624117
Cerebral Infarction Associate 26708676
Cognition Disorders Associate 36624117
Disruptive Impulse Control and Conduct Disorders Associate 36624117
Migraine Disorders Associate 26231841
Neoplasm Metastasis Associate 16164832
Renal Insufficiency Associate 27247127
Stroke Associate 26708676