NOBOX

NOBOX oogenesis homeobox

Summary

This homeobox gene encodes a transcription factor that is thought to play a role in oogenesis. In mice, it is essential for folliculogenesis and regulation of oocyte-specific genes. Defects in this gene result in premature ovarian failure type 5.[provided by RefSeq, May 2011]

Known Variants135 total

rsidPosition (GRCh37)AllelesClassClinVar
rs12082157:144,094,130C/T—benign
rs573068807:144,094,256A/C—benign
rs778020987:144,094,418T/C—benign
rs20538999687:144,094,429G/C—uncertain significance
rs13845576117:144,094,448G/A—uncertain significance
rs13998593477:144,094,461C/T—uncertain significance
rs1169371277:144,094,471T/C—uncertain significance
rs7738781827:144,094,484G/A—uncertain significance
rs7627878787:144,094,502G/T—uncertain significance
rs12136689247:144,094,508G/A—uncertain significance
rs8860620377:144,094,509G/T—uncertain significance
rs10460416307:144,094,534A/G—uncertain significance
rs1462273017:144,094,553G/A—benign
rs1390833527:144,094,560G/A—uncertain significance
rs13332150537:144,094,562C/T—uncertain significance
rs20539015017:144,094,579G/C—uncertain significance
rs1158825747:144,094,583G/A—conflicting classifications of pathogenicity
rs14740753537:144,094,606C/A—uncertain significance
rs12082167:144,094,613G/T—benign
rs1498805247:144,094,642G/T—benign
rs755748427:144,094,718C/T—likely benign
rs12082177:144,094,783A/G—benign
rs1421470257:144,095,357C/T—likely benign
rs7494342307:144,095,364C/T—uncertain significance
rs13322073187:144,095,390G/A—uncertain significance
rs8860620387:144,095,398A/C—uncertain significance
rs10211252057:144,095,434C/T—uncertain significance
rs3718742787:144,095,440G/A—benign
rs3748791717:144,095,451G/A—conflicting classifications of pathogenicity
rs5726846327:144,095,458C/T—uncertain significance
rs9914087247:144,095,490C/T—likely benign
rs3702034527:144,095,500G/A—uncertain significance
rs13352926017:144,095,557G/A—uncertain significance
rs10098273557:144,095,586C/G—uncertain significance
rs26995037:144,095,600A/G—benign
rs5316628587:144,095,603G/A—conflicting classifications of pathogenicity
rs5591752267:144,095,642G/C—uncertain significance
rs12032316957:144,095,662G/C—uncertain significance
rs7626484907:144,095,666G/T—conflicting classifications of pathogenicity
rs119795287:144,095,730C/T—benign
rs26995027:144,095,880T/C—benign
rs7527758567:144,096,029C/T—uncertain significance
rs3761692087:144,096,030G/A—likely benign
rs7589132137:144,096,038C/T—uncertain significance
rs3761684567:144,096,062A/G—uncertain significance
rs5357982837:144,096,064G/A—uncertain significance
rs5545062077:144,096,065G/C—uncertain significance
rs25257027:144,096,068C/T—benign
rs10064634397:144,096,072C/G—likely pathogenic
rs14671517397:144,096,081G/T—uncertain significance
rs1121901167:144,096,158C/T—benign
rs7764555197:144,096,175G/A—uncertain significance
rs7630872987:144,096,176G/A—uncertain significance
rs7677023717:144,096,190G/C—uncertain significance
rs3716735007:144,096,194G/A—uncertain significance
rs7805663867:144,096,205C/T—uncertain significance
rs14760859357:144,096,214C/A—likely pathogenic
rs5765567667:144,096,241G/C—uncertain significance
rs7467718907:144,096,262A/T—uncertain significance
rs7766091917:144,096,269G/A—uncertain significance
rs117697877:144,096,456C/T—benign
rs7488103007:144,096,508G/A—uncertain significance
rs5684924787:144,096,531G/A—likely pathogenic
rs117698477:144,096,598C/T—benign
rs1855660027:144,096,772C/Tintron variant—
rs7573887:144,096,839A/G—benign
rs1893065757:144,096,892T/G—uncertain significance
rs1995386897:144,096,925C/T—likely benign
rs12186208937:144,096,926G/A—likely pathogenic
rs7548041257:144,096,938G/A—uncertain significance
rs2019476777:144,096,940C/Tmissense variantpathogenic
rs1933031047:144,096,956C/Amissense variantpathogenic
rs7671104787:144,096,966G/T—uncertain significance
rs7650590517:144,097,216G/A—likely benign
rs5333303647:144,097,219C/T—uncertain significance
rs1933031037:144,097,225C/Gmissense variantpathogenic
rs7504479437:144,097,235C/T—uncertain significance
rs3722220517:144,097,262C/T—uncertain significance
rs7602232617:144,097,273G/A—uncertain significance
rs7539303137:144,097,327G/A—uncertain significance
rs2004237457:144,097,342C/T—uncertain significance
rs1933031027:144,097,343G/Astop gainedpathogenic
rs7474970427:144,097,355T/C—uncertain significance
rs13290868807:144,097,382T/C—uncertain significance
rs10295519347:144,098,144C/T—uncertain significance
rs7740633347:144,098,189G/A—uncertain significance
rs21288616587:144,098,192G/A—uncertain significance
rs3765980187:144,098,241G/A—uncertain significance
rs7606754117:144,098,280A/G—uncertain significance
rs7621395237:144,098,304G/A—uncertain significance
rs7508624387:144,098,324G/A—uncertain significance
rs3746558497:144,098,332T/A—likely benign
rs3720718207:144,098,355T/C—uncertain significance
rs14285004867:144,098,370T/C—uncertain significance
rs2014232777:144,098,419T/C—likely benign
rs7543106267:144,098,444G/A—uncertain significance
rs5585073387:144,098,495C/T—uncertain significance
rs3721656907:144,098,496G/C—likely benign
rs2018063977:144,098,529C/T—benign
rs24861186777:144,098,567C/T—uncertain significance

Showing 100 of 135 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.

NOBOX — NOBOX oogenesis homeobox