TSPAN9
tetraspanin 9
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. Alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Nov 2009]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10744592 | 12:3,209,494 | C/G | intron variant | — |
| rs7963344 | 12:3,231,716 | C/T | intron variant | — |
| rs7980759 | 12:3,231,752 | A/G | intron variant | — |
| rs35096434 | 12:3,232,679 | C/T | regulatory region variant | — |
| rs11062517 | 12:3,235,839 | C/A | — | — |
| rs34071646 | 12:3,238,142 | A/G | intron variant | — |
| rs71458040 | 12:3,239,079 | C/A | intron variant | — |
| rs489296 | 12:3,239,167 | T/G | intron variant | — |
| rs878962 | 12:3,287,279 | G/T | intron variant | — |
| rs748977531 | 12:3,310,381 | T/C | — | uncertain significance |
| rs2098371549 | 12:3,310,419 | C/G | — | uncertain significance |
| rs11062578 | 12:3,327,167 | G/A | intron variant | — |
| rs3782812 | 12:3,339,809 | C/A | — | — |
| rs7976853 | 12:3,340,657 | C/T | regulatory region variant | — |
| rs7979282 | 12:3,341,040 | G/A | — | — |
| rs7979731 | 12:3,351,523 | C/G | — | — |
| rs3825343 | 12:3,365,426 | C/G | — | — |
| rs11062596 | 12:3,367,761 | A/T | intron variant | — |
| rs74891390 | 12:3,373,823 | G/C | intron variant | — |
| rs1038076071 | 12:3,387,617 | A/G | — | uncertain significance |
| rs773297242 | 12:3,387,687 | A/C | — | uncertain significance |
| rs1862834976 | 12:3,387,688 | C/A | — | uncertain significance |
| rs565330967 | 12:3,387,689 | C/A | — | uncertain significance |
| rs142466845 | 12:3,387,698 | G/A | — | uncertain significance |
| rs1197689885 | 12:3,387,702 | T/C | — | uncertain significance |
| rs2497909712 | 12:3,387,768 | T/G | — | uncertain significance |
| rs754646751 | 12:3,388,162 | T/G | — | uncertain significance |
| rs66462026 | 12:3,390,197 | C/T | intron variant | — |
| rs371175944 | 12:3,390,368 | G/A | — | uncertain significance |
| rs747741255 | 12:3,390,472 | G/A | — | likely benign |
| rs71577847 | 12:3,390,952 | G/T | — | uncertain significance |
| rs1382972594 | 12:3,390,965 | G/A | — | uncertain significance |
| rs139045775 | 12:3,390,976 | T/C | — | uncertain significance |
| rs149866702 | 12:3,392,223 | G/A | — | uncertain significance |
| rs67551338 | 12:3,393,100 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.