| Symbol: Name: ID: |
TSPAN7 tetraspanin 7 GFS:1668 |
| Gene name: | TSPAN7 |
| Chromosome: | Xp11.4 |
| Previous Symbols: | MXS1, TM4SF2, MRX58 |
| Previous Names: | transmembrane 4 superfamily member 2, "mental retardation, X-linked 58" |
| Aliases: | DXS1692E, TALLA-1, A15, CD231 |
| Name Aliases: | |
| Locus Type: | gene with protein product |
| Mouse Genome Database ID: | MGI:1298407 | Rat Genome Database ID: | RGD:1589725 |
| HGNC ID: | HGNC:11854 | RefSeq IDs: | NM_004615 |
| Entrez Gene ID: | 7102 | Ensembl Gene ID: | ENSG00000156298 |
| VEGA IDs: | OTTHUMG00000024090 | UniProt ID: | P41732 |
| UCSC ID: | uc004deg.3 | OMIM ID: | 300096 |
| Pubmed: | PMID12070254 | ||
| CCDS IDs: | CCDSCCDS14248.1 | ||
Tetraspanin-7 is a protein that in humans is encoded by the TSPAN7 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 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 mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy. [provided by RefSeq]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Function: May be involved in cell proliferation and cell motility.
Products for TSPAN7 gene
| Catalog | Product Name | Application | Company |
| GFS:E01668 | tetraspanin 7; ELISA kit | ELISA | n/a |
| GFS:A01668 | tetraspanin 7; Anti | ANTIBODIES | n/a |
| GFS:P01668 | tetraspanin 7; Protien | Protien | n/a |