TSPAN7 tetraspanin 7 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 7102)
Symbol: TSPAN7
Full name: tetraspanin 7
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: A15; CCG-B7; CD231; DXS1692E; MRX58; MXS1; TALLA-1; TM4SF2; TM4SF2b; XLID58
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 signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked cognitive disability and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy. [provided by RefSeq, Jul 2008]
Expression: Broad expression in brain (RPKM 306.6), adrenal (RPKM 70.3) and 14 other tissues
Orthologs: mouse
Gene size: 127377bp
Exon count: 8