TRPC7
transient receptor potential cation channel subfamily C member 7
Summary
Predicted to enable inositol 1,4,5 trisphosphate binding activity and store-operated calcium channel activity. Predicted to be involved in calcium ion transmembrane transport; regulation of cytosolic calcium ion concentration; and single fertilization. Predicted to be located in membrane; nuclear envelope; and perinuclear region of cytoplasm. Predicted to be part of cation channel complex. Predicted to be active in plasma membrane. Implicated in lung cancer. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1173368432 | 5:135,549,148 | C/T | — | uncertain significance |
| rs768651273 | 5:135,551,950 | C/T | — | uncertain significance |
| rs751702897 | 5:135,561,790 | G/A | — | uncertain significance |
| rs376972495 | 5:135,567,111 | G/A | — | likely benign |
| rs756214253 | 5:135,567,161 | C/T | — | uncertain significance |
| rs1755816028 | 5:135,567,232 | T/C | — | uncertain significance |
| rs11748198 | 5:135,575,829 | C/A | intron variant | — |
| rs184633300 | 5:135,580,526 | A/G | intron variant | — |
| rs892191417 | 5:135,583,184 | C/T | — | uncertain significance |
| rs760900591 | 5:135,583,189 | C/T | — | uncertain significance |
| rs755662783 | 5:135,583,370 | C/T | — | uncertain significance |
| rs371141920 | 5:135,587,409 | C/T | — | uncertain significance |
| rs1756526889 | 5:135,587,451 | G/A | — | uncertain significance |
| rs745537292 | 5:135,587,465 | G/A | — | uncertain significance |
| rs748913544 | 5:135,587,535 | C/T | — | uncertain significance |
| rs76839573 | 5:135,594,091 | C/T | intron variant | — |
| rs372364792 | 5:135,601,945 | G/T | — | uncertain significance |
| rs1196926705 | 5:135,602,027 | C/T | — | uncertain significance |
| rs199816122 | 5:135,610,475 | T/A | — | uncertain significance |
| rs181309464 | 5:135,623,369 | G/A | intron variant | — |
| rs139357022 | 5:135,632,724 | G/T | intron variant | — |
| rs13189315 | 5:135,636,726 | C/T | upstream gene variant | — |
| rs13189678 | 5:135,636,959 | C/T | regulatory region variant | — |
| rs35118298 | 5:135,648,692 | A/G | intron variant | — |
| rs185392119 | 5:135,650,310 | T/C | intron variant | — |
| rs2479711934 | 5:135,651,296 | C/T | — | uncertain significance |
| rs754976469 | 5:135,651,419 | C/G | — | uncertain significance |
| rs55972276 | 5:135,653,737 | C/G | — | — |
| rs183251928 | 5:135,672,342 | C/T | intron variant | — |
| rs11956571 | 5:135,672,435 | T/C | intron variant | — |
| rs950716 | 5:135,680,540 | A/G | intron variant | — |
| rs147261777 | 5:135,685,631 | G/C | intron variant | — |
| rs745468742 | 5:135,692,370 | C/T | — | uncertain significance |
| rs1207634906 | 5:135,692,461 | C/G | — | uncertain significance |
| rs932646076 | 5:135,692,750 | G/A | — | uncertain significance |
| rs536224426 | 5:135,692,795 | G/A | — | uncertain significance |
| rs777935954 | 5:135,692,835 | C/A | — | uncertain significance |
| rs2479819182 | 5:135,692,863 | G/T | — | uncertain significance |
| rs577536758 | 5:135,693,039 | G/A | — | uncertain significance |
| rs2479819875 | 5:135,693,043 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.