CSNK1G3
casein kinase 1 gamma 3
Summary
This gene encodes a member of a family of serine/threonine protein kinases that phosphorylate caseins and other acidic proteins. A related protein in the African clawed frog participates in the transmission of Wnt/beta-catenin signaling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7728713 | 5:122,847,678 | G/C | — | — |
| rs7734476 | 5:122,848,876 | G/C | — | — |
| rs4530754 | 5:122,855,416 | G/C | — | — |
| rs6595454 | 5:122,858,907 | A/T | intron variant | — |
| rs78154385 | 5:122,858,945 | A/G | intron variant | — |
| rs9327301 | 5:122,860,170 | G/A | intron variant | — |
| rs12188944 | 5:122,868,279 | G/A | — | — |
| rs2407781 | 5:122,877,037 | C/T | intron variant | — |
| rs2547002443 | 5:122,881,374 | A/G | — | uncertain significance |
| rs2547107173 | 5:122,888,815 | A/T | — | uncertain significance |
| rs10066772 | 5:122,890,823 | T/C | intron variant | — |
| rs7447793 | 5:122,896,447 | T/C | intron variant | — |
| rs11241702 | 5:122,902,603 | A/C | — | — |
| rs6595460 | 5:122,908,468 | A/G | intron variant | — |
| rs141615513 | 5:122,909,102 | T/C | — | uncertain significance |
| rs139101160 | 5:122,909,132 | A/G | — | uncertain significance |
| rs955032767 | 5:122,909,195 | C/T | — | uncertain significance |
| rs748402581 | 5:122,911,568 | C/T | — | uncertain significance |
| rs17150492 | 5:122,916,804 | A/G | intron variant | — |
| rs7709540 | 5:122,917,860 | T/G | — | — |
| rs1340519639 | 5:122,924,166 | C/T | — | uncertain significance |
| rs1895233 | 5:122,924,864 | G/T | intron variant | — |
| rs1377474749 | 5:122,926,199 | G/A | — | uncertain significance |
| rs947091551 | 5:122,927,029 | C/G | — | uncertain significance |
| rs2547552183 | 5:122,927,068 | C/G | — | uncertain significance |
| rs58466006 | 5:122,928,965 | A/G | intron variant | — |
| rs141285750 | 5:122,930,822 | G/A | — | likely benign |
| rs114475286 | 5:122,940,412 | A/G | — | benign |
| rs184548649 | 5:122,940,414 | A/G | — | likely benign |
| rs1335600106 | 5:122,940,418 | G/T | — | uncertain significance |
| rs955530337 | 5:122,940,428 | C/T | — | uncertain significance |
| rs143856483 | 5:122,950,072 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.