Entity Details

Primary name TSN7_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP41732
EntryNameTSN7_HUMAN
FullNameTetraspanin-7
TaxID9606
Evidenceevidence at protein level
Length249
SequenceStatuscomplete
DateCreated1995-11-01
DateModified2021-04-07

Ontological Relatives

GenesTSPAN7

GO terms

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

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000301 Tetraspanin, animalsFamilyFamily
IPR008952 Tetraspanin, EC2 domain superfamilyFamilyHomologous superfamily
IPR018499 Tetraspanin/PeripherinFamilyFamily
IPR018503 Tetraspanin, conserved siteSiteConserved site

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.