DIXDC1
DIX domain containing 1
Summary
The protein encoded by this gene is a positive regulator of the Wnt signaling pathway. The encoded protein is found associated with gamma tubulin at the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199945833 | 11:111,808,278 | A/G | — | benign |
| rs587774805 | 11:111,815,768 | C/T | — | — |
| rs2498095265 | 11:111,835,328 | C/T | — | uncertain significance |
| rs370213735 | 11:111,835,336 | C/G | — | uncertain significance |
| rs377157480 | 11:111,835,393 | G/A | — | uncertain significance |
| rs782259747 | 11:111,839,339 | G/A | — | uncertain significance |
| rs1859812070 | 11:111,839,350 | A/G | — | uncertain significance |
| rs199891499 | 11:111,844,828 | C/T | — | uncertain significance |
| rs587723931 | 11:111,844,843 | G/A | — | uncertain significance |
| rs782515563 | 11:111,844,923 | G/A | — | uncertain significance |
| rs930647209 | 11:111,845,632 | C/T | — | uncertain significance |
| rs781863884 | 11:111,851,496 | A/C | — | uncertain significance |
| rs782742979 | 11:111,851,499 | G/A | — | uncertain significance |
| rs1419374563 | 11:111,853,087 | C/T | — | likely pathogenic |
| rs200647738 | 11:111,853,096 | C/T | — | uncertain significance |
| rs182278039 | 11:111,857,624 | T/C | — | benign |
| rs373126732 | 11:111,859,774 | A/T | missense variant | — |
| rs2498247218 | 11:111,864,220 | A/C | — | uncertain significance |
| rs2498248903 | 11:111,864,434 | G/T | — | uncertain significance |
| rs140140857 | 11:111,865,381 | T/C | intron variant | — |
| rs10789855 | 11:111,866,015 | C/T | — | — |
| rs587638080 | 11:111,873,414 | C/T | — | — |
| rs114428192 | 11:111,887,482 | C/A | — | uncertain significance |
| rs184718561 | 11:111,887,493 | C/T | missense variant | — |
| rs650461 | 11:111,889,635 | C/G | downstream gene variant | — |
| rs781973280 | 11:111,889,738 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.