CADPS
calcium dependent secretion activator
Summary
This gene encodes a novel neural/endocrine-specific cytosolic and peripheral membrane protein required for the Ca2+-regulated exocytosis of secretory vesicles. The protein acts at a stage in exocytosis that follows ATP-dependent priming, which involves the essential synthesis of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). Alternative splicing has been observed at this locus and three variants, encoding distinct isoforms, are described. [provided by RefSeq, Aug 2008]
Known Variants97 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79260062 | 3:62,385,269 | G/A | — | likely benign |
| rs111793843 | 3:62,386,350 | C/T | intron variant | — |
| rs775583072 | 3:62,388,775 | G/A | — | uncertain significance |
| rs200558042 | 3:62,388,816 | C/T | — | likely benign |
| rs558289554 | 3:62,388,836 | C/T | — | uncertain significance |
| rs199626657 | 3:62,388,848 | T/C | — | likely benign |
| rs1707040888 | 3:62,388,858 | T/C | — | uncertain significance |
| rs771045473 | 3:62,423,871 | C/A | — | uncertain significance |
| rs144155979 | 3:62,431,456 | T/C | — | uncertain significance |
| rs1158576022 | 3:62,451,085 | C/A | — | uncertain significance |
| rs574220713 | 3:62,451,122 | C/T | — | uncertain significance |
| rs746556427 | 3:62,452,043 | T/C | — | uncertain significance |
| rs566908931 | 3:62,459,841 | T/C | — | likely benign |
| rs779869722 | 3:62,459,846 | A/C | — | uncertain significance |
| rs367714345 | 3:62,459,939 | C/T | — | uncertain significance |
| rs781377421 | 3:62,459,985 | C/T | — | uncertain significance |
| rs375576173 | 3:62,467,401 | G/A | — | uncertain significance |
| rs368961255 | 3:62,467,427 | C/T | — | likely benign |
| rs373178609 | 3:62,467,434 | G/A | — | uncertain significance |
| rs77008736 | 3:62,467,521 | T/A | — | likely benign |
| rs376315928 | 3:62,477,973 | C/T | — | uncertain significance |
| rs2535035692 | 3:62,477,985 | T/C | — | uncertain significance |
| rs774402470 | 3:62,478,113 | C/T | — | likely benign |
| rs13325751 | 3:62,478,194 | C/T | intron variant | — |
| rs145339043 | 3:62,479,314 | A/G | — | benign |
| rs1229955756 | 3:62,484,866 | G/T | — | uncertain significance |
| rs142613294 | 3:62,484,892 | C/T | — | uncertain significance |
| rs781177687 | 3:62,484,932 | G/A | — | uncertain significance |
| rs76105684 | 3:62,494,438 | A/G | — | — |
| rs150724919 | 3:62,501,769 | T/C | — | uncertain significance |
| rs774721337 | 3:62,501,778 | G/A | — | uncertain significance |
| rs760619126 | 3:62,502,271 | A/C | — | uncertain significance |
| rs141962517 | 3:62,514,061 | T/C | intron variant | — |
| rs765741289 | 3:62,518,617 | A/G | — | likely benign |
| rs371505343 | 3:62,522,174 | C/G | — | uncertain significance |
| rs764524930 | 3:62,522,199 | T/G | — | uncertain significance |
| rs185882358 | 3:62,522,255 | G/A | — | likely benign |
| rs2077060028 | 3:62,535,595 | G/A | — | uncertain significance |
| rs142524771 | 3:62,535,626 | C/T | — | uncertain significance |
| rs2077067728 | 3:62,535,650 | G/C | — | uncertain significance |
| rs372017906 | 3:62,535,796 | A/G | — | likely benign |
| rs76254845 | 3:62,543,096 | G/A | — | benign |
| rs898296147 | 3:62,543,142 | G/A | — | uncertain significance |
| rs567840502 | 3:62,556,597 | C/T | — | uncertain significance |
| rs1288369724 | 3:62,556,608 | A/G | — | uncertain significance |
| rs833653 | 3:62,560,813 | T/C | intron variant | — |
| rs60992373 | 3:62,570,854 | A/G | — | benign |
| rs140246088 | 3:62,570,980 | G/A | — | uncertain significance |
| rs865829911 | 3:62,571,009 | A/G | — | likely benign |
| rs139420058 | 3:62,578,414 | G/A | — | likely benign |
| rs1231831 | 3:62,601,366 | T/C | regulatory region variant | — |
| rs144979381 | 3:62,631,467 | C/T | — | uncertain significance |
| rs146070021 | 3:62,636,542 | C/T | — | uncertain significance |
| rs143096441 | 3:62,636,543 | G/A | — | likely benign |
| rs74991517 | 3:62,636,579 | G/A | — | benign |
| rs2479660480 | 3:62,636,606 | G/T | — | uncertain significance |
| rs768044590 | 3:62,636,652 | G/A | — | uncertain significance |
| rs532422453 | 3:62,636,885 | C/T | — | — |
| rs772423610 | 3:62,648,009 | T/C | — | uncertain significance |
| rs773569176 | 3:62,648,017 | C/T | — | uncertain significance |
| rs538579 | 3:62,711,674 | G/C | intron variant | — |
| rs557951 | 3:62,713,263 | T/G | regulatory region variant | — |
| rs539100 | 3:62,714,917 | T/C | — | — |
| rs488273 | 3:62,716,800 | G/C | intron variant | — |
| rs580384 | 3:62,733,366 | C/G | — | — |
| rs374963507 | 3:62,739,146 | G/A | — | likely benign |
| rs189008412 | 3:62,739,149 | C/A | — | uncertain significance |
| rs2487231882 | 3:62,739,218 | T/G | — | likely benign |
| rs774706010 | 3:62,739,237 | G/A | — | uncertain significance |
| rs142877891 | 3:62,739,320 | G/A | — | likely benign |
| rs372234823 | 3:62,739,325 | C/T | — | uncertain significance |
| rs149627119 | 3:62,739,389 | G/A | — | likely benign |
| rs35975017 | 3:62,739,395 | G/A | — | benign |
| rs199602219 | 3:62,739,434 | G/A | — | likely benign |
| rs768387474 | 3:62,751,567 | G/A | — | likely benign |
| rs374048491 | 3:62,751,607 | T/C | — | uncertain significance |
| rs193921128 | 3:62,751,617 | C/T | — | uncertain significance |
| rs559119461 | 3:62,755,698 | T/G | — | — |
| rs304172 | 3:62,782,468 | G/C | — | — |
| rs2083317268 | 3:62,860,284 | T/G | — | uncertain significance |
| rs140977565 | 3:62,860,354 | C/T | — | likely benign |
| rs2547612315 | 3:62,860,447 | G/A | — | likely benign |
| rs1200827323 | 3:62,860,475 | C/T | — | uncertain significance |
| rs543179326 | 3:62,860,498 | C/T | — | likely benign |
| rs2547616825 | 3:62,860,506 | T/G | — | uncertain significance |
| rs1329096152 | 3:62,860,509 | C/T | — | uncertain significance |
| rs1335105830 | 3:62,860,556 | C/T | — | uncertain significance |
| rs2083388019 | 3:62,860,562 | A/C | — | uncertain significance |
| rs1451372707 | 3:62,860,565 | C/G | — | likely benign |
| rs2547623971 | 3:62,860,578 | C/T | — | uncertain significance |
| rs2547624167 | 3:62,860,581 | A/C | — | uncertain significance |
| rs751422032 | 3:62,860,617 | C/T | — | uncertain significance |
| rs757218775 | 3:62,860,622 | G/T | — | uncertain significance |
| rs745876740 | 3:62,860,630 | G/C | — | likely benign |
| rs938732449 | 3:62,860,645 | G/T | — | likely benign |
| rs772478182 | 3:62,860,649 | C/T | — | uncertain significance |
| rs1234944909 | 3:62,860,694 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.