Entity Details

Primary name TSPAN7
Entity type gene
Source Source Link

Details

PrimaryID7102
RefseqGeneNG_009160
SymbolTSPAN7
Nametetraspanin 7
ChromosomeX
LocationXp11.4
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-24
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTSN7_HUMAN

GO terms

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GOName
GO:0005887 integral component of plasma membrane
GO:0016032 viral process

Diseases

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Disease IDSourceNameDescription
300210 OMIMMental retardation, X-linked 58 (MRX58)A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. The disease is caused by variants affecting the gene represented in this entry.