CPXM1
carboxypeptidase X, M14 family member 1
Summary
This gene likely encodes a member of the carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a carboxypeptidase domain, but the protein appears to lack residues necessary for carboxypeptidase activity.[provided by RefSeq, May 2010]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367832059 | 20:2,774,859 | G/A | — | uncertain significance |
| rs767745837 | 20:2,774,867 | C/T | — | uncertain significance |
| rs41297632 | 20:2,774,910 | G/A | — | benign |
| rs1399524279 | 20:2,774,918 | A/G | — | uncertain significance |
| rs138143188 | 20:2,774,984 | C/T | — | uncertain significance |
| rs142149554 | 20:2,774,985 | G/A | — | uncertain significance |
| rs746665380 | 20:2,774,990 | T/C | — | likely benign |
| rs200652644 | 20:2,774,994 | G/A | — | uncertain significance |
| rs2514964807 | 20:2,775,197 | T/C | — | uncertain significance |
| rs369610590 | 20:2,775,213 | C/T | — | uncertain significance |
| rs1375704500 | 20:2,775,245 | G/A | — | uncertain significance |
| rs2514964930 | 20:2,775,248 | T/C | — | uncertain significance |
| rs781462252 | 20:2,776,256 | G/A | — | uncertain significance |
| rs149777086 | 20:2,776,287 | C/T | — | uncertain significance |
| rs538584869 | 20:2,776,293 | C/A | — | likely benign |
| rs764257542 | 20:2,776,319 | C/T | — | uncertain significance |
| rs201409887 | 20:2,776,334 | T/C | — | uncertain significance |
| rs777608220 | 20:2,776,355 | G/A | — | uncertain significance |
| rs147693328 | 20:2,776,377 | G/T | — | uncertain significance |
| rs766944887 | 20:2,776,389 | C/T | — | uncertain significance |
| rs746775795 | 20:2,776,412 | C/A | — | uncertain significance |
| rs376401302 | 20:2,776,440 | C/T | — | uncertain significance |
| rs757432903 | 20:2,776,715 | C/A | — | uncertain significance |
| rs772776734 | 20:2,776,776 | C/T | — | uncertain significance |
| rs1447574378 | 20:2,776,930 | G/C | — | uncertain significance |
| rs368774043 | 20:2,776,931 | A/T | — | uncertain significance |
| rs758834400 | 20:2,776,933 | G/A | — | uncertain significance |
| rs769586671 | 20:2,776,949 | G/A | — | uncertain significance |
| rs1453540234 | 20:2,777,062 | C/T | — | uncertain significance |
| rs1242164012 | 20:2,777,080 | T/C | — | uncertain significance |
| rs1222438352 | 20:2,777,660 | T/C | — | uncertain significance |
| rs144323253 | 20:2,777,691 | A/G | — | benign |
| rs148800823 | 20:2,777,707 | G/A | — | likely benign |
| rs763737973 | 20:2,777,710 | G/A | — | uncertain significance |
| rs868316533 | 20:2,777,904 | G/A | — | uncertain significance |
| rs2514974559 | 20:2,778,823 | T/C | — | uncertain significance |
| rs1195354489 | 20:2,778,833 | C/T | — | likely benign |
| rs145548069 | 20:2,778,906 | C/T | — | uncertain significance |
| rs573430362 | 20:2,779,088 | G/A | — | uncertain significance |
| rs761333983 | 20:2,779,130 | C/T | — | uncertain significance |
| rs140809004 | 20:2,779,138 | C/T | — | likely benign |
| rs771960978 | 20:2,779,139 | G/A | — | uncertain significance |
| rs772440702 | 20:2,779,390 | C/T | — | uncertain significance |
| rs2514976957 | 20:2,779,423 | C/T | — | uncertain significance |
| rs138905387 | 20:2,779,485 | A/G | — | uncertain significance |
| rs201037077 | 20:2,779,513 | G/C | — | uncertain significance |
| rs215543 | 20:2,780,151 | G/A | regulatory region variant | — |
| rs1033994266 | 20:2,781,085 | T/C | — | likely benign |
| rs1020907511 | 20:2,781,101 | A/C | — | uncertain significance |
| rs537783470 | 20:2,781,158 | C/G | — | uncertain significance |
| rs545736822 | 20:2,781,341 | C/G | — | — |
| rs6132968 | 20:2,783,121 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.