CATSPERD
catsper channel auxiliary subunit delta
Summary
Predicted to be involved in flagellated sperm motility and sperm capacitation. Predicted to be located in plasma membrane. Predicted to be part of CatSper complex. Predicted to be active in sperm principal piece. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758511219 | 19:5,724,860 | A/G | — | uncertain significance |
| rs1481590494 | 19:5,727,294 | C/T | — | uncertain significance |
| rs2512475775 | 19:5,727,333 | A/G | — | uncertain significance |
| rs747649810 | 19:5,729,929 | C/T | — | uncertain significance |
| rs1355730634 | 19:5,733,892 | C/T | — | uncertain significance |
| rs1408382585 | 19:5,733,903 | G/T | — | uncertain significance |
| rs201875294 | 19:5,733,931 | A/C | — | uncertain significance |
| rs1245632990 | 19:5,733,974 | G/A | — | uncertain significance |
| rs370046981 | 19:5,737,200 | G/C | — | uncertain significance |
| rs200285271 | 19:5,739,337 | C/T | — | uncertain significance |
| rs371002531 | 19:5,739,367 | C/T | — | uncertain significance |
| rs199601443 | 19:5,739,368 | G/A | — | likely benign |
| rs536263465 | 19:5,740,491 | G/A | — | — |
| rs770610933 | 19:5,744,462 | G/A | — | uncertain significance |
| rs540346018 | 19:5,744,501 | C/G | — | uncertain significance |
| rs764538602 | 19:5,744,505 | T/C | — | uncertain significance |
| rs762200295 | 19:5,746,014 | G/A | — | uncertain significance |
| rs529155205 | 19:5,748,192 | G/A | — | likely benign |
| rs201831364 | 19:5,748,208 | C/A | — | likely benign |
| rs774003666 | 19:5,749,127 | C/A | — | uncertain significance |
| rs371150801 | 19:5,749,139 | G/A | — | uncertain significance |
| rs12608476 | 19:5,751,430 | A/T | intron variant | — |
| rs1464528891 | 19:5,751,675 | C/G | — | uncertain significance |
| rs371947428 | 19:5,751,740 | G/A | — | uncertain significance |
| rs886962910 | 19:5,751,779 | T/A | — | uncertain significance |
| rs891764996 | 19:5,751,794 | C/T | — | uncertain significance |
| rs201746413 | 19:5,751,802 | A/C | — | uncertain significance |
| rs762098314 | 19:5,754,146 | G/C | — | uncertain significance |
| rs763844202 | 19:5,754,219 | C/T | — | likely benign |
| rs1357778822 | 19:5,757,875 | T/G | — | uncertain significance |
| rs775543468 | 19:5,763,264 | T/C | — | uncertain significance |
| rs1174201094 | 19:5,766,164 | G/C | — | uncertain significance |
| rs777262174 | 19:5,768,189 | G/A | — | uncertain significance |
| rs771400884 | 19:5,768,198 | A/G | — | uncertain significance |
| rs1358603518 | 19:5,771,064 | T/C | — | uncertain significance |
| rs938967755 | 19:5,772,815 | T/C | — | uncertain significance |
| rs189734613 | 19:5,772,888 | C/T | — | uncertain significance |
| rs1007916638 | 19:5,772,894 | A/G | — | uncertain significance |
| rs778837999 | 19:5,772,918 | C/T | — | uncertain significance |
| rs773568657 | 19:5,772,956 | C/G | — | uncertain significance |
| rs766353123 | 19:5,776,203 | A/G | — | uncertain significance |
| rs1012319079 | 19:5,776,205 | G/T | — | uncertain significance |
| rs2512693002 | 19:5,776,268 | A/C | — | uncertain significance |
| rs201309746 | 19:5,776,274 | G/A | — | likely benign |
| rs756814020 | 19:5,776,323 | A/G | — | uncertain significance |
| rs72985145 | 19:5,776,973 | A/T | intron variant | — |
| rs777770581 | 19:5,778,403 | A/G | — | uncertain significance |
| rs554429104 | 19:5,778,538 | G/A | — | uncertain significance |
| rs532197714 | 19:5,778,548 | G/A | — | uncertain significance |
| rs772577885 | 19:5,778,559 | A/G | — | uncertain significance |
| rs1004219961 | 19:5,778,560 | A/G | — | likely benign |
| rs2512700043 | 19:5,778,569 | C/T | — | uncertain significance |
| rs1371236993 | 19:5,778,577 | T/C | — | uncertain significance |
| rs137867416 | 19:5,778,593 | C/T | — | uncertain significance |
| rs201809671 | 19:5,778,602 | A/G | — | uncertain significance |
| rs941913431 | 19:5,778,637 | G/A | — | uncertain significance |
| rs2512700496 | 19:5,778,641 | C/T | — | uncertain significance |
| rs1213718606 | 19:5,778,647 | G/A | — | uncertain significance |
| rs373865922 | 19:5,778,649 | C/T | — | uncertain significance |
| rs17852929 | 19:5,778,655 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.