Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10100
Gene name Gene Name - the full gene name approved by the HGNC.
Tetraspanin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TSPAN2
Synonyms (NCBI Gene) Gene synonyms aliases
NET3, TSN2, TSPAN-2
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613133 20659 ENSG00000134198
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Mild obesity-related type 2 diabetes N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease 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