MKRN2
makorin ring finger protein 2
Summary
This gene encodes a probable E3 ubiquitin ligase containing several zinc finger domains, that is a member of the makorin RING zinc-finger protein family. This gene overlaps the v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1) gene in an antisense orientation and may have a co-regulatory function with RAF1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs753601501 | 3:12,610,493 | C/T | — | uncertain significance |
| rs1986068 | 3:12,610,732 | T/C | intron variant | — |
| rs773116580 | 3:12,611,581 | C/A | — | uncertain significance |
| rs779808828 | 3:12,611,641 | C/T | — | uncertain significance |
| rs746670442 | 3:12,611,651 | C/G | — | uncertain significance |
| rs368353653 | 3:12,611,668 | C/G | — | uncertain significance |
| rs374230709 | 3:12,611,719 | G/A | — | uncertain significance |
| rs753356310 | 3:12,613,631 | G/A | — | uncertain significance |
| rs372538092 | 3:12,613,633 | G/C | — | uncertain significance |
| rs768823128 | 3:12,613,661 | C/T | — | uncertain significance |
| rs2470142356 | 3:12,613,670 | A/G | — | uncertain significance |
| rs373294185 | 3:12,613,729 | G/A | — | uncertain significance |
| rs748431588 | 3:12,613,750 | G/A | — | uncertain significance |
| rs769797562 | 3:12,613,759 | G/A | — | uncertain significance |
| rs749411483 | 3:12,613,862 | C/T | — | uncertain significance |
| rs2648308 | 3:12,614,107 | T/G | — | — |
| rs79836657 | 3:12,615,964 | G/A | regulatory region variant | — |
| rs713178 | 3:12,615,984 | T/C | regulatory region variant | — |
| rs1346193567 | 3:12,618,153 | T/G | — | uncertain significance |
| rs73130305 | 3:12,621,075 | C/T | downstream gene variant | — |
| rs929328808 | 3:12,623,404 | G/A | — | uncertain significance |
| rs1310104345 | 3:12,623,618 | T/C | — | uncertain significance |
| rs763839801 | 3:12,623,630 | C/T | — | uncertain significance |
| rs1317334247 | 3:12,623,631 | G/A | — | uncertain significance |
| rs201937482 | 3:12,623,670 | T/A | — | uncertain significance |
| rs765319030 | 3:12,623,676 | A/G | — | likely benign |
| rs554403152 | 3:12,623,690 | G/A | — | uncertain significance |
| rs771144793 | 3:12,623,705 | G/A | — | uncertain significance |
| rs546564318 | 3:12,623,708 | G/T | missense variant | — |
| rs1477039101 | 3:12,623,715 | T/G | — | uncertain significance |
| rs768466464 | 3:12,623,720 | C/A | — | uncertain significance |
| rs34924942 | 3:12,623,722 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.