TSPAN15
tetraspanin 15
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. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112843485 | 10:71,211,707 | T/C | regulatory region variant | — |
| rs12265956 | 10:71,214,101 | T/C | intron variant | — |
| rs12241097 | 10:71,216,678 | T/G | regulatory region variant | — |
| rs12776158 | 10:71,218,094 | T/C | intron variant | — |
| rs10823378 | 10:71,218,566 | C/T | regulatory region variant | — |
| rs10762296 | 10:71,218,719 | G/C | — | — |
| rs58719473 | 10:71,218,889 | A/G | — | — |
| rs67069429 | 10:71,227,429 | C/T | — | — |
| rs7917677 | 10:71,240,574 | T/C | intron variant | — |
| rs2052964 | 10:71,242,429 | A/T | intron variant | — |
| rs2052965 | 10:71,242,461 | A/G | intron variant | — |
| rs12241216 | 10:71,242,945 | A/T | — | — |
| rs10998832 | 10:71,243,032 | C/T | intron variant | — |
| rs1386647523 | 10:71,243,471 | G/C | — | uncertain significance |
| rs1841787978 | 10:71,243,489 | G/A | — | uncertain significance |
| rs750879012 | 10:71,243,496 | G/A | — | uncertain significance |
| rs140708891 | 10:71,243,586 | T/C | — | uncertain significance |
| rs745864673 | 10:71,243,630 | G/C | — | uncertain significance |
| rs1268469835 | 10:71,244,928 | T/C | — | uncertain significance |
| rs35426769 | 10:71,244,942 | G/A | — | uncertain significance |
| rs150067289 | 10:71,244,945 | G/A | — | uncertain significance |
| rs78707713 | 10:71,245,276 | T/A | — | — |
| rs1365796665 | 10:71,255,359 | T/C | — | uncertain significance |
| rs771032542 | 10:71,258,051 | G/A | — | uncertain significance |
| rs780839062 | 10:71,258,090 | G/A | — | uncertain significance |
| rs1227969 | 10:71,263,264 | C/T | intron variant | — |
| rs1842322012 | 10:71,265,908 | T/A | — | uncertain significance |
| rs2540655173 | 10:71,265,977 | T/C | — | uncertain significance |
| rs143125761 | 10:71,266,697 | C/T | — | uncertain significance |
| rs148515448 | 10:71,266,703 | G/T | — | uncertain significance |
| rs142000918 | 10:71,266,706 | C/T | — | uncertain significance |
| rs1364370984 | 10:71,266,719 | G/T | — | uncertain significance |
| rs10823398 | 10:71,270,363 | C/G | — | — |
| rs4999704 | 10:71,299,319 | G/C | — | — |
| rs2999170 | 10:71,303,133 | C/T | intergenic variant | — |
| rs143945190 | 10:71,303,923 | A/G | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.