PRDM10
PR/SET domain 10
Summary
The protein encoded by this gene is a transcription factor that contains C2H2-type zinc-fingers. It also contains a positive regulatory domain, which has been found in several other zinc-finger transcription factors including those involved in B cell differentiation and tumor suppression. Studies of the mouse counterpart suggest that this protein may be involved in the development of the central nerve system (CNS), as well as in the pathogenesis of neuronal storage disease. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1783908 | 11:129,770,482 | G/A | upstream gene variant | — |
| rs181420995 | 11:129,772,240 | C/T | — | uncertain significance |
| rs775825856 | 11:129,772,246 | C/T | — | uncertain significance |
| rs1461300656 | 11:129,772,393 | C/T | — | uncertain significance |
| rs201374213 | 11:129,772,402 | C/G | — | uncertain significance |
| rs775532074 | 11:129,775,622 | T/G | — | uncertain significance |
| rs751925955 | 11:129,780,412 | T/C | — | uncertain significance |
| rs141740226 | 11:129,780,436 | T/G | — | likely benign |
| rs1309569109 | 11:129,780,454 | A/G | — | uncertain significance |
| rs147100201 | 11:129,780,494 | A/T | — | benign |
| rs141397814 | 11:129,782,003 | C/T | — | uncertain significance |
| rs202214464 | 11:129,782,080 | A/G | — | uncertain significance |
| rs2497053545 | 11:129,784,639 | T/C | — | uncertain significance |
| rs1411653788 | 11:129,784,667 | C/T | — | uncertain significance |
| rs2497054902 | 11:129,784,783 | C/T | — | uncertain significance |
| rs1322235735 | 11:129,784,875 | C/G | — | uncertain significance |
| rs148854421 | 11:129,785,583 | G/A | — | uncertain significance |
| rs200112746 | 11:129,785,625 | G/A | — | uncertain significance |
| rs138407751 | 11:129,785,670 | C/T | — | uncertain significance |
| rs1950385709 | 11:129,787,119 | G/A | — | uncertain significance |
| rs1486222419 | 11:129,788,493 | C/T | — | uncertain significance |
| rs200278867 | 11:129,788,543 | C/T | — | uncertain significance |
| rs1319176059 | 11:129,793,159 | C/T | — | uncertain significance |
| rs148098393 | 11:129,794,871 | C/T | — | uncertain significance |
| rs983210115 | 11:129,794,940 | T/C | — | uncertain significance |
| rs896327755 | 11:129,795,007 | G/A | — | uncertain significance |
| rs564662147 | 11:129,800,951 | G/A | — | uncertain significance |
| rs80125038 | 11:129,801,022 | T/C | — | benign |
| rs572787698 | 11:129,802,046 | C/A | — | uncertain significance |
| rs749333068 | 11:129,802,050 | T/C | — | uncertain significance |
| rs764743532 | 11:129,802,109 | C/T | — | uncertain significance |
| rs1345811167 | 11:129,805,053 | G/C | — | uncertain significance |
| rs2497213864 | 11:129,812,341 | C/T | — | uncertain significance |
| rs1486661396 | 11:129,812,408 | G/T | — | uncertain significance |
| rs151309947 | 11:129,812,451 | G/A | — | uncertain significance |
| rs150441931 | 11:129,812,492 | C/A | — | uncertain significance |
| rs141414113 | 11:129,812,530 | C/T | — | benign |
| rs146397050 | 11:129,814,697 | G/A | — | uncertain significance |
| rs116002683 | 11:129,814,723 | G/A | — | benign |
| rs372199751 | 11:129,817,055 | C/T | — | uncertain significance |
| rs775019050 | 11:129,817,064 | G/A | — | uncertain significance |
| rs907233043 | 11:129,817,075 | G/A | — | uncertain significance |
| rs910497766 | 11:129,817,136 | C/T | — | uncertain significance |
| rs76174913 | 11:129,817,155 | C/T | — | benign |
| rs374643047 | 11:129,817,169 | C/G | — | uncertain significance |
| rs149863373 | 11:129,817,175 | T/C | — | likely benign |
| rs1301490249 | 11:129,825,448 | C/T | — | uncertain significance |
| rs78900720 | 11:129,827,700 | T/A | — | benign |
| rs377181650 | 11:129,827,731 | C/G | — | uncertain significance |
| rs7130078 | 11:129,850,215 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.