WDR25
WD repeat domain 25
Summary
This gene encodes a protein containing 7 WD repeats. WD repeats are approximately 30 to 40-amino acid domains containing several conserved residues, typically having a Tryptophan-Aspartic acid dipeptide (WD) at the C-terminal end. WD domains are involved in protein-protein interactions in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1566879949 | 14:100,847,274 | A/G | — | uncertain significance |
| rs190371335 | 14:100,847,281 | C/A | — | uncertain significance |
| rs78359884 | 14:100,847,338 | A/G | — | uncertain significance |
| rs373487922 | 14:100,847,343 | G/A | — | uncertain significance |
| rs2549328298 | 14:100,847,374 | A/G | — | uncertain significance |
| rs747425518 | 14:100,847,401 | G/A | — | likely benign |
| rs757671200 | 14:100,847,413 | C/T | — | uncertain significance |
| rs550629799 | 14:100,847,559 | G/A | — | likely benign |
| rs771039905 | 14:100,847,581 | T/C | — | uncertain significance |
| rs199637878 | 14:100,847,682 | A/G | — | uncertain significance |
| rs373109465 | 14:100,847,788 | A/G | — | uncertain significance |
| rs142235833 | 14:100,847,799 | A/G | — | uncertain significance |
| rs151218015 | 14:100,847,850 | G/T | — | uncertain significance |
| rs375660046 | 14:100,847,884 | C/G | — | uncertain significance |
| rs544294755 | 14:100,847,898 | G/A | — | uncertain significance |
| rs377508410 | 14:100,847,929 | C/T | — | uncertain significance |
| rs943000461 | 14:100,847,964 | C/A | — | uncertain significance |
| rs1472629599 | 14:100,848,066 | A/G | — | uncertain significance |
| rs11624075 | 14:100,852,739 | G/A | regulatory region variant | — |
| rs565214185 | 14:100,860,073 | A/G | — | — |
| rs10144321 | 14:100,882,405 | A/G | regulatory region variant | — |
| rs755347286 | 14:100,934,358 | G/T | — | uncertain significance |
| rs796052162 | 14:100,934,375 | C/A | — | likely benign |
| rs746445610 | 14:100,934,377 | C/G | — | uncertain significance |
| rs199801334 | 14:100,934,430 | C/T | — | uncertain significance |
| rs559488785 | 14:100,934,448 | C/T | — | uncertain significance |
| rs138735540 | 14:100,934,449 | G/A | — | likely benign |
| rs575934571 | 14:100,975,880 | A/C | — | — |
| rs7492565 | 14:100,985,577 | G/A | — | — |
| rs367815944 | 14:100,992,342 | C/T | — | uncertain significance |
| rs9805992 | 14:100,993,651 | A/C | — | — |
| rs1416997199 | 14:100,995,425 | C/G | — | uncertain significance |
| rs772922376 | 14:100,995,435 | C/T | — | uncertain significance |
| rs2549427939 | 14:100,996,172 | G/T | — | uncertain significance |
| rs755752616 | 14:100,996,250 | C/T | — | uncertain significance |
| rs774745695 | 14:100,996,302 | G/A | — | uncertain significance |
| rs762275292 | 14:100,996,311 | A/G | — | uncertain significance |
| rs147626247 | 14:100,996,319 | G/A | — | uncertain significance |
| rs144754220 | 14:100,996,337 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.