CATSPERG
catsper channel auxiliary subunit gamma
Summary
CATSPERG is a subunit of the CATSPER (see CATSPER1; MIM 606389) sperm calcium channel, which is required for sperm hyperactivated motility and male fertility (Wang et al., 2009 [PubMed 19516020]).[supplied by OMIM, Jul 2010]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761209613 | 19:38,827,890 | A/G | — | uncertain significance |
| rs1960472989 | 19:38,827,963 | T/C | — | uncertain significance |
| rs1384695874 | 19:38,827,969 | C/T | — | uncertain significance |
| rs777650361 | 19:38,828,112 | A/C | — | likely benign |
| rs752988469 | 19:38,828,267 | A/G | — | uncertain significance |
| rs763670233 | 19:38,828,273 | C/A | — | uncertain significance |
| rs775087783 | 19:38,834,254 | C/T | — | uncertain significance |
| rs983115015 | 19:38,834,301 | T/A | — | uncertain significance |
| rs907550847 | 19:38,834,302 | T/A | — | uncertain significance |
| rs749267952 | 19:38,834,312 | G/C | — | uncertain significance |
| rs1191706385 | 19:38,834,321 | G/T | — | uncertain significance |
| rs1460163898 | 19:38,834,350 | C/G | — | uncertain significance |
| rs547897343 | 19:38,834,356 | G/A | — | uncertain significance |
| rs375537032 | 19:38,834,710 | C/T | — | uncertain significance |
| rs1969989442 | 19:38,834,936 | G/C | — | uncertain significance |
| rs1379716221 | 19:38,837,127 | C/T | — | uncertain significance |
| rs551833511 | 19:38,837,147 | A/G | — | uncertain significance |
| rs758453597 | 19:38,837,153 | G/A | — | uncertain significance |
| rs1366216301 | 19:38,837,235 | C/G | — | uncertain significance |
| rs985710593 | 19:38,842,987 | G/C | — | uncertain significance |
| rs755811756 | 19:38,843,069 | A/T | — | uncertain significance |
| rs774060715 | 19:38,845,410 | A/G | — | uncertain significance |
| rs146516371 | 19:38,845,439 | C/T | — | uncertain significance |
| rs754443545 | 19:38,845,443 | C/T | — | uncertain significance |
| rs1016682571 | 19:38,845,470 | A/C | — | uncertain significance |
| rs768563593 | 19:38,845,485 | G/C | — | likely benign |
| rs770653802 | 19:38,847,132 | G/A | — | uncertain significance |
| rs774196898 | 19:38,847,474 | C/T | — | uncertain significance |
| rs771650795 | 19:38,848,935 | C/G | — | likely benign |
| rs879895093 | 19:38,849,141 | G/C | — | uncertain significance |
| rs773023618 | 19:38,849,156 | C/T | — | uncertain significance |
| rs576285566 | 19:38,850,187 | G/A | — | likely benign |
| rs201664540 | 19:38,850,214 | C/T | — | uncertain significance |
| rs60071299 | 19:38,850,246 | G/A | downstream gene variant | — |
| rs200118141 | 19:38,851,142 | T/C | — | uncertain significance |
| rs376608525 | 19:38,851,160 | T/C | — | uncertain significance |
| rs150667046 | 19:38,851,387 | A/C | — | uncertain significance |
| rs200471284 | 19:38,851,419 | G/A | — | likely benign |
| rs1970331645 | 19:38,851,441 | T/C | — | uncertain significance |
| rs2513723863 | 19:38,852,440 | C/T | — | uncertain significance |
| rs374892753 | 19:38,853,058 | G/A | — | uncertain significance |
| rs757106735 | 19:38,853,143 | A/C | — | uncertain significance |
| rs753544913 | 19:38,853,372 | A/G | — | uncertain significance |
| rs1028334910 | 19:38,853,444 | T/C | — | uncertain significance |
| rs73043037 | 19:38,856,372 | T/A | upstream gene variant | — |
| rs146429794 | 19:38,857,910 | G/A | — | uncertain significance |
| rs958361735 | 19:38,857,922 | C/G | — | uncertain significance |
| rs201823945 | 19:38,857,946 | C/T | — | uncertain significance |
| rs373200243 | 19:38,858,196 | G/A | — | uncertain significance |
| rs141648079 | 19:38,858,394 | C/T | — | uncertain significance |
| rs1453030523 | 19:38,858,749 | A/G | — | uncertain significance |
| rs78474816 | 19:38,860,458 | C/T | upstream gene variant | — |
| rs756023189 | 19:38,860,631 | G/A | — | uncertain significance |
| rs766441123 | 19:38,860,839 | T/C | — | uncertain significance |
| rs780837428 | 19:38,860,879 | G/A | — | uncertain significance |
| rs1970528737 | 19:38,861,169 | T/C | — | uncertain significance |
| rs549955953 | 19:38,861,181 | T/C | — | uncertain significance |
| rs148618826 | 19:38,861,208 | G/A | — | uncertain significance |
| rs374950558 | 19:38,861,217 | C/T | — | uncertain significance |
| rs757579145 | 19:38,861,232 | G/A | — | likely benign |
| rs768674555 | 19:38,861,248 | C/T | — | uncertain significance |
| rs555054175 | 19:38,861,304 | G/A | — | uncertain significance |
| rs376077607 | 19:38,861,316 | G/A | — | likely benign |
| rs748083478 | 19:38,861,323 | C/T | — | uncertain significance |
| rs371589723 | 19:38,861,370 | T/C | — | uncertain significance |
| rs145481167 | 19:38,861,409 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.