GSC

goosecoid homeobox

Summary

This gene encodes a member of the bicoid subfamily of the paired (PRD) homeobox family of proteins. The encoded protein acts as a transcription factor and may be autoregulatory. A similar protein in mice plays a role in craniofacial and rib cage development during embryogenesis. [provided by RefSeq, Jul 2008]

Known Variants73 total

rsidPosition (GRCh37)AllelesClassClinVar
rs385040214:95,234,452G/T——
rs128419104014:95,234,858T/C—likely benign
rs54361214614:95,234,917C/A—uncertain significance
rs92552772814:95,234,951C/A—likely benign
rs390504914:95,235,109C/A—benign
rs119740633814:95,235,286G/A—likely benign
rs104891023914:95,235,287G/A—likely benign
rs77029334614:95,235,288C/T—likely benign
rs37681081314:95,235,304C/G—uncertain significance
rs129761582714:95,235,320A/G—uncertain significance
rs75048706214:95,235,339C/T—uncertain significance
rs121749224214:95,235,344G/A—uncertain significance
rs75812354914:95,235,346G/A—uncertain significance
rs74671293414:95,235,355C/T—likely benign
rs11755562014:95,235,358G/A—benign
rs213970312714:95,235,363T/G—uncertain significance
rs250356092414:95,235,371T/C—uncertain significance
rs77606990214:95,235,418G/A—likely benign
rs74980456314:95,235,421G/A—likely benign
rs14941096314:95,235,448C/A—uncertain significance
rs250356127914:95,235,453T/C—uncertain significance
rs142260954014:95,235,465G/A—likely benign
rs76509135214:95,235,473C/T—uncertain significance
rs14477703714:95,235,490G/A—benign
rs75688047114:95,235,495T/C—uncertain significance
rs58777728914:95,235,510G/Astop gainedpathogenic
rs11623202214:95,235,740G/A—benign
rs53737418214:95,235,987C/G—likely benign
rs58777729014:95,235,997C/G—pathogenic
rs117669468014:95,236,014G/A—likely benign
rs140768584114:95,236,028G/C—uncertain significance
rs144197697214:95,236,038C/T—likely benign
rs102586706914:95,236,052C/T—uncertain significance
rs95168442714:95,236,097C/G—uncertain significance
rs250356283814:95,236,101G/A—likely benign
rs188524639914:95,236,117C/T—uncertain significance
rs250356289214:95,236,125G/T—likely benign
rs76160044214:95,236,130C/G—uncertain significance
rs14593225214:95,236,139C/T—benign
rs188524784914:95,236,162G/T—uncertain significance
rs93656425414:95,236,164G/A—likely benign
rs188524801714:95,236,165G/C—uncertain significance
rs188524807314:95,236,168A/C—uncertain significance
rs96418767714:95,236,170G/A—likely benign
rs188524821014:95,236,171G/T—uncertain significance
rs75570445114:95,236,173G/A—likely benign
rs54587899914:95,236,179G/A—benign
rs188524856014:95,236,180T/G—uncertain significance
rs93399139314:95,236,182G/A—likely benign
rs250356319514:95,236,183A/C—uncertain significance
rs250356320614:95,236,187C/A—uncertain significance
rs75556729714:95,236,192T/G—uncertain significance
rs37020748014:95,236,194G/A—benign
rs147692078014:95,236,201G/A—uncertain significance
rs148939455314:95,236,207C/T—uncertain significance
rs53131044614:95,236,208C/T—uncertain significance
rs74729544314:95,236,217C/A—uncertain significance
rs19135287214:95,236,245C/T—likely benign
rs134823988714:95,236,253C/T—uncertain significance
rs76043992214:95,236,264G/A—uncertain significance
rs250356349514:95,236,265C/T—uncertain significance
rs250356353714:95,236,272G/A—likely benign
rs100620221914:95,236,276G/A—uncertain significance
rs76608341014:95,236,278C/G—likely benign
rs146891669014:95,236,280C/T—uncertain significance
rs75341416414:95,236,284C/G—uncertain significance
rs86711334814:95,236,307G/A—uncertain significance
rs159515804814:95,236,326G/A—likely benign
rs102975937414:95,236,328C/G—uncertain significance
rs20089999814:95,236,342C/T—uncertain significance
rs52913066114:95,236,347G/T—likely benign
rs6070254114:95,236,570A/G—benign
rs716126614:95,236,707A/G—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.