TRPC1
transient receptor potential cation channel subfamily C member 1
Summary
The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748211039 | 3:142,443,421 | C/G | — | uncertain significance |
| rs770125446 | 3:142,443,451 | C/T | — | uncertain significance |
| rs760081567 | 3:142,443,465 | T/C | — | uncertain significance |
| rs185773990 | 3:142,443,488 | C/A | — | uncertain significance |
| rs777998269 | 3:142,443,507 | G/A | — | uncertain significance |
| rs571028288 | 3:142,443,520 | T/G | — | uncertain significance |
| rs953239 | 3:142,446,205 | A/G | — | — |
| rs552784808 | 3:142,454,699 | G/C | — | — |
| rs750429181 | 3:142,455,302 | G/A | — | uncertain significance |
| rs758528510 | 3:142,455,304 | A/C | — | uncertain significance |
| rs2472959415 | 3:142,467,164 | T/C | — | uncertain significance |
| rs767750507 | 3:142,467,175 | C/T | — | uncertain significance |
| rs7638459 | 3:142,490,151 | T/C | intron variant | — |
| rs1935828342 | 3:142,496,512 | C/T | — | uncertain significance |
| rs1935831265 | 3:142,496,584 | G/C | — | uncertain significance |
| rs757739566 | 3:142,499,780 | C/G | — | uncertain significance |
| rs193920786 | 3:142,503,555 | C/T | — | uncertain significance |
| rs751261909 | 3:142,503,735 | T/C | — | uncertain significance |
| rs1351318056 | 3:142,503,853 | T/C | — | uncertain significance |
| rs1560113862 | 3:142,503,861 | C/T | — | uncertain significance |
| rs758894493 | 3:142,509,926 | C/T | — | uncertain significance |
| rs765355502 | 3:142,511,670 | A/G | — | uncertain significance |
| rs745396101 | 3:142,511,763 | G/A | — | uncertain significance |
| rs200537637 | 3:142,522,824 | T/C | — | uncertain significance |
| rs1282476550 | 3:142,522,928 | G/A | — | uncertain significance |
| rs2473147724 | 3:142,522,950 | A/G | — | uncertain significance |
| rs762854141 | 3:142,525,020 | A/G | — | uncertain significance |
| rs759693044 | 3:142,525,040 | G/A | — | uncertain significance |
| rs371348586 | 3:142,525,055 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.