PRSS23
serine protease 23
Summary
This gene encodes a conserved member of the trypsin family of serine proteases. Mouse studies found a decrease of mRNA levels of this gene after ovulation was induced. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11606902 | 11:86,500,201 | C/T | upstream gene variant | — |
| rs2015747 | 11:86,503,137 | C/A | intron variant | — |
| rs2000538 | 11:86,505,072 | C/G | intron variant | — |
| rs148849426 | 11:86,518,703 | G/A | — | likely benign |
| rs576671301 | 11:86,518,708 | T/G | — | uncertain significance |
| rs751626725 | 11:86,518,728 | C/T | — | uncertain significance |
| rs1391694807 | 11:86,518,737 | G/A | — | uncertain significance |
| rs149461457 | 11:86,518,753 | C/T | — | uncertain significance |
| rs776970288 | 11:86,518,791 | C/T | — | uncertain significance |
| rs1007282341 | 11:86,518,813 | A/C | — | uncertain significance |
| rs140723937 | 11:86,518,814 | G/T | — | uncertain significance |
| rs143933691 | 11:86,518,851 | G/A | — | likely benign |
| rs2497090445 | 11:86,518,863 | G/C | — | uncertain significance |
| rs575669604 | 11:86,518,951 | C/T | — | uncertain significance |
| rs144740366 | 11:86,518,963 | A/G | — | uncertain significance |
| rs564570104 | 11:86,519,001 | C/T | — | uncertain significance |
| rs374469283 | 11:86,519,037 | T/C | — | uncertain significance |
| rs368713993 | 11:86,519,059 | G/A | — | uncertain significance |
| rs148223020 | 11:86,519,070 | C/A | — | uncertain significance |
| rs200816081 | 11:86,519,158 | C/T | — | uncertain significance |
| rs549222243 | 11:86,519,208 | C/G | — | uncertain significance |
| rs1220066743 | 11:86,519,235 | G/A | — | uncertain significance |
| rs747536133 | 11:86,519,278 | A/G | — | uncertain significance |
| rs1205151750 | 11:86,519,365 | C/T | — | uncertain significance |
| rs376594317 | 11:86,519,485 | C/T | — | uncertain significance |
| rs775668009 | 11:86,519,583 | G/A | — | uncertain significance |
| rs201412660 | 11:86,519,654 | G/C | — | uncertain significance |
| rs764233584 | 11:86,519,751 | A/G | — | uncertain significance |
| rs190825105 | 11:86,619,769 | G/A | intron variant | — |
| rs4567493 | 11:86,634,423 | A/T | — | — |
| rs149504726 | 11:86,653,988 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.