HOXC9

homeobox C9

Summary

This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. [provided by RefSeq, Jul 2008]

Known Variants18 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5636810512:54,393,770A/Gcoding sequence variant—
rs1281709212:54,393,774G/Tcoding sequence variant—
rs5615454212:54,393,783G/Ccoding sequence variant—
rs254019101012:54,393,988C/T—uncertain significance
rs254019106112:54,394,027G/A—uncertain significance
rs77384909212:54,394,051A/G—uncertain significance
rs57525750312:54,394,249A/C—uncertain significance
rs20035872112:54,394,274C/G—uncertain significance
rs3407960612:54,394,284C/Tsynonymous variant—
rs1182994812:54,394,337C/T—benign
rs126373316212:54,394,361G/T—uncertain significance
rs76296795512:54,394,385A/C—uncertain significance
rs75016823612:54,394,397T/A—uncertain significance
rs224182012:54,394,497C/Asynonymous variant—
rs254019327612:54,396,216A/C—uncertain significance
rs75779033712:54,396,244G/A—uncertain significance
rs143887309612:54,396,336C/T—uncertain significance
rs77764358712:54,396,375C/T—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.