CDYL
chromodomain Y like
Summary
Chromodomain Y is a primate-specific Y-chromosomal gene family expressed exclusively in the testis and implicated in infertility. Although the Y-linked genes are testis-specific, this autosomal gene is ubiquitously expressed. The Y-linked genes arose by retrotransposition of an mRNA from this gene, followed by amplification of the retroposed gene. Proteins encoded by this gene superfamily possess a chromodomain, a motif implicated in chromatin binding and gene suppression, and a catalytic domain believed to be involved in histone acetylation. Multiple proteins are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9504244 | 6:4,765,002 | G/A | intron variant | — |
| rs58544878 | 6:4,777,680 | C/A | regulatory region variant | — |
| rs761567588 | 6:4,790,535 | A/G | — | — |
| rs73717741 | 6:4,874,759 | C/G | regulatory region variant | — |
| rs200651601 | 6:4,892,094 | C/T | — | uncertain significance |
| rs2480339903 | 6:4,892,110 | A/C | — | uncertain significance |
| rs762836740 | 6:4,892,182 | C/T | — | uncertain significance |
| rs759040134 | 6:4,892,280 | A/G | — | uncertain significance |
| rs374024219 | 6:4,892,310 | C/T | — | uncertain significance |
| rs758795798 | 6:4,892,311 | G/A | — | uncertain significance |
| rs139710301 | 6:4,892,334 | T/A | — | uncertain significance |
| rs371998448 | 6:4,892,367 | G/T | — | uncertain significance |
| rs755337916 | 6:4,892,391 | G/A | — | uncertain significance |
| rs147719814 | 6:4,892,430 | G/A | — | uncertain significance |
| rs150926278 | 6:4,892,484 | G/A | — | uncertain significance |
| rs1008812563 | 6:4,892,553 | C/T | — | uncertain significance |
| rs375314618 | 6:4,892,574 | A/G | — | uncertain significance |
| rs199558668 | 6:4,892,583 | A/G | — | uncertain significance |
| rs2480542511 | 6:4,935,781 | A/G | — | uncertain significance |
| rs746042185 | 6:4,935,782 | A/G | — | uncertain significance |
| rs778247904 | 6:4,937,835 | G/A | — | uncertain significance |
| rs1342878630 | 6:4,937,841 | G/A | — | uncertain significance |
| rs145710209 | 6:4,937,871 | G/A | — | uncertain significance |
| rs372880737 | 6:4,937,925 | A/G | — | uncertain significance |
| rs376971832 | 6:4,952,518 | A/G | — | uncertain significance |
| rs771507480 | 6:4,952,608 | G/A | — | uncertain significance |
| rs200558204 | 6:4,952,641 | G/C | — | uncertain significance |
| rs775840808 | 6:4,954,232 | C/T | — | uncertain significance |
| rs1561729465 | 6:4,954,239 | G/C | — | uncertain significance |
| rs1758792864 | 6:4,954,250 | C/T | — | uncertain significance |
| rs138000187 | 6:4,954,279 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.