DKK2
dickkopf Wnt signaling pathway inhibitor 2
Summary
This gene encodes a protein that is a member of the dickkopf family. The secreted protein contains two cysteine rich regions and is involved in embryonic development through its interactions with the Wnt signaling pathway. It can act as either an agonist or antagonist of Wnt/beta-catenin signaling, depending on the cellular context and the presence of the co-factor kremen 2. Activity of this protein is also modulated by binding to the Wnt co-receptor LDL-receptor related protein 6 (LRP6). [provided by RefSeq, Jul 2008]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs419558 | 4:107,844,092 | C/T | 3 prime UTR variant | — |
| rs419764 | 4:107,844,157 | C/T | 3 prime UTR variant | — |
| rs1282726784 | 4:107,845,152 | A/T | — | uncertain significance |
| rs768079972 | 4:107,845,197 | C/T | — | uncertain significance |
| rs753265155 | 4:107,845,239 | G/A | — | uncertain significance |
| rs772632334 | 4:107,845,325 | C/G | — | uncertain significance |
| rs374743911 | 4:107,845,717 | T/A | — | uncertain significance |
| rs1348128917 | 4:107,845,758 | T/C | — | uncertain significance |
| rs17037102 | 4:107,845,794 | C/A | missense variant | — |
| rs541386879 | 4:107,847,018 | C/T | — | uncertain significance |
| rs202160269 | 4:107,847,028 | T/C | — | uncertain significance |
| rs769686573 | 4:107,847,037 | A/G | — | uncertain significance |
| rs201073614 | 4:107,847,106 | C/T | — | uncertain significance |
| rs447372 | 4:107,853,996 | G/A | intron variant | — |
| rs145945174 | 4:107,861,949 | G/A | intron variant | — |
| rs77571736 | 4:107,864,984 | G/T | — | — |
| rs17037148 | 4:107,883,068 | C/T | intron variant | — |
| rs147012957 | 4:107,956,729 | C/T | — | uncertain significance |
| rs772738812 | 4:107,956,742 | C/T | — | uncertain significance |
| rs3733635 | 4:107,956,905 | A/G | 5 prime UTR variant | — |
| rs1379062425 | 4:108,229,177 | G/A | — | likely benign |
| rs568876472 | 4:108,229,209 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.