HOXD10 Chromosome 2

Homeobox D10
6 variants 6 Health Risk

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What This Gene Does
This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as "rocker-bottom foot" deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
HOXL subclass homeoboxes
Locus Type
gene with protein product
Location
2q31.1
Ensembl
ENSG00000128710
Associated Conditions (1)
Congenital vertical talus
Key Variants
All Variants (6)
RSID Category Clinical Significance Conditions
RS143870330 Health Risk Conflicting classifications of pathogenicity Congenital vertical talus, Congenital vertical talus
RS149038150 Health Risk Conflicting classifications of pathogenicity Congenital vertical talus, Congenital vertical talus
RS374700658 Health Risk Conflicting classifications of pathogenicity Congenital vertical talus, Congenital vertical talus
RS532592274 Health Risk Conflicting classifications of pathogenicity Congenital vertical talus, Congenital vertical talus
RS769981285 Health Risk Conflicting classifications of pathogenicity Congenital vertical talus, Congenital vertical talus
RS104893634 Health Risk Pathogenic Congenital vertical talus, Congenital vertical talus
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