SPATC1L
spermatogenesis and centriole associated 1 like
Summary
Enables identical protein binding activity. Predicted to be involved in spermatogenesis. Predicted to act upstream of or within actin polymerization or depolymerization; positive regulation of cAMP-dependent protein kinase activity; and positive regulation of cAMP/PKA signal transduction. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs559670239 | 21:47,581,301 | C/T | — | uncertain significance |
| rs1348887826 | 21:47,581,394 | T/C | — | uncertain significance |
| rs749029733 | 21:47,581,405 | C/T | — | uncertain significance |
| rs14378 | 21:47,581,423 | T/C | — | benign |
| rs1290857121 | 21:47,581,424 | T/C | — | uncertain significance |
| rs146895208 | 21:47,581,435 | T/A | — | uncertain significance |
| rs771485808 | 21:47,581,453 | C/T | — | uncertain significance |
| rs770223525 | 21:47,581,470 | G/C | — | uncertain significance |
| rs772927581 | 21:47,581,490 | C/T | — | uncertain significance |
| rs547788669 | 21:47,581,498 | G/A | — | likely benign |
| rs74518516 | 21:47,581,508 | C/A | — | benign |
| rs774810232 | 21:47,581,513 | C/T | — | uncertain significance |
| rs373386591 | 21:47,581,537 | C/A | — | uncertain significance |
| rs750400397 | 21:47,581,549 | G/A | — | uncertain significance |
| rs1453380315 | 21:47,581,559 | G/A | — | uncertain significance |
| rs745355464 | 21:47,581,574 | G/A | — | uncertain significance |
| rs2517106255 | 21:47,581,616 | A/G | — | uncertain significance |
| rs113710653 | 21:47,581,835 | C/T | missense variant | benign |
| rs372429503 | 21:47,581,837 | A/G | — | uncertain significance |
| rs139199473 | 21:47,581,869 | G/A | — | likely benign |
| rs2517107811 | 21:47,581,871 | A/G | — | uncertain significance |
| rs752185329 | 21:47,581,897 | T/C | — | uncertain significance |
| rs575362573 | 21:47,581,910 | G/A | — | uncertain significance |
| rs145843473 | 21:47,581,934 | C/T | — | uncertain significance |
| rs113146399 | 21:47,581,949 | C/T | — | benign |
| rs76486812 | 21:47,581,961 | C/T | — | likely benign |
| rs1030274449 | 21:47,581,968 | G/T | — | uncertain significance |
| rs541120391 | 21:47,581,977 | G/C | — | uncertain significance |
| rs369043715 | 21:47,588,224 | T/C | — | uncertain significance |
| rs141566688 | 21:47,588,268 | G/C | — | uncertain significance |
| rs771728448 | 21:47,588,275 | G/A | — | uncertain significance |
| rs760668765 | 21:47,588,297 | G/A | — | uncertain significance |
| rs1035329275 | 21:47,588,308 | C/G | — | uncertain significance |
| rs759481276 | 21:47,588,408 | G/A | — | uncertain significance |
| rs757252512 | 21:47,588,453 | C/T | — | uncertain significance |
| rs750914245 | 21:47,588,455 | G/A | — | uncertain significance |
| rs1034893922 | 21:47,588,489 | G/A | — | uncertain significance |
| rs2079558990 | 21:47,588,521 | T/G | — | uncertain significance |
| rs540248819 | 21:47,588,536 | G/A | — | uncertain significance |
| rs1206125393 | 21:47,588,551 | G/A | — | uncertain significance |
| rs553756950 | 21:47,602,633 | C/T | — | uncertain significance |
| rs913515766 | 21:47,602,685 | C/T | — | uncertain significance |
| rs143719440 | 21:47,602,691 | C/T | — | likely benign |
| rs796920051 | 21:47,605,027 | C/T | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.