MIOS
meiosis regulator for oocyte development
Summary
Predicted to enable zinc ion binding activity. Involved in cellular response to amino acid starvation; positive regulation of TORC1 signaling; and protein-containing complex localization. Located in several cellular components, including cytosol; lysosomal membrane; and nucleoplasm. Part of GATOR2 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs972600 | 7:7,604,656 | G/T | — | — |
| rs766345026 | 7:7,612,113 | G/A | — | uncertain significance |
| rs751689193 | 7:7,612,248 | G/A | — | uncertain significance |
| rs749609580 | 7:7,612,287 | C/A | — | uncertain significance |
| rs2534429541 | 7:7,612,540 | G/C | — | uncertain significance |
| rs767881518 | 7:7,612,561 | C/A | — | uncertain significance |
| rs374466007 | 7:7,612,578 | A/T | — | uncertain significance |
| rs1783404699 | 7:7,612,602 | G/A | — | uncertain significance |
| rs1428064398 | 7:7,612,722 | C/T | — | uncertain significance |
| rs777015316 | 7:7,612,770 | G/A | — | uncertain significance |
| rs1783413238 | 7:7,612,847 | G/C | — | uncertain significance |
| rs367954045 | 7:7,612,853 | A/G | — | likely benign |
| rs1384415475 | 7:7,612,947 | G/A | — | uncertain significance |
| rs372901269 | 7:7,612,970 | G/A | — | likely benign |
| rs201095729 | 7:7,613,118 | A/G | — | uncertain significance |
| rs895454538 | 7:7,613,137 | A/G | — | uncertain significance |
| rs189971963 | 7:7,613,194 | T/C | — | uncertain significance |
| rs772120205 | 7:7,613,275 | T/C | — | uncertain significance |
| rs564046020 | 7:7,613,307 | A/G | — | uncertain significance |
| rs375686147 | 7:7,613,319 | G/C | — | uncertain significance |
| rs1427739869 | 7:7,613,336 | G/C | — | uncertain significance |
| rs1783431098 | 7:7,613,355 | G/A | — | uncertain significance |
| rs770365061 | 7:7,613,392 | C/T | — | uncertain significance |
| rs771655781 | 7:7,613,755 | G/A | — | uncertain significance |
| rs2534443362 | 7:7,613,800 | A/G | — | uncertain significance |
| rs1165552550 | 7:7,622,865 | A/G | — | uncertain significance |
| rs369299032 | 7:7,622,866 | C/T | — | uncertain significance |
| rs758834768 | 7:7,622,898 | C/A | — | uncertain significance |
| rs377331148 | 7:7,622,945 | C/G | — | uncertain significance |
| rs773449075 | 7:7,622,959 | G/A | — | uncertain significance |
| rs759882781 | 7:7,622,971 | A/G | — | uncertain significance |
| rs2534550240 | 7:7,625,347 | A/G | — | uncertain significance |
| rs117761453 | 7:7,625,367 | A/G | — | benign |
| rs2534572060 | 7:7,628,153 | G/A | — | uncertain significance |
| rs201263722 | 7:7,629,117 | A/G | — | uncertain significance |
| rs191766303 | 7:7,630,745 | A/G | intron variant | — |
| rs201892249 | 7:7,634,674 | T/G | — | uncertain significance |
| rs201081552 | 7:7,634,744 | G/T | — | uncertain significance |
| rs752251286 | 7:7,634,758 | G/C | — | uncertain significance |
| rs748191896 | 7:7,636,001 | T/G | — | likely benign |
| rs147346205 | 7:7,638,741 | A/G | intron variant | — |
| rs377596054 | 7:7,642,051 | T/G | — | — |
| rs775304759 | 7:7,645,636 | A/G | — | uncertain significance |
| rs2534720410 | 7:7,645,683 | C/G | — | uncertain significance |
| rs774075805 | 7:7,646,648 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.