HOXD10 homeobox D10 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 3236)
Source: NCBI Gene (ID 3236)
Symbol: HOXD10
Full name: homeobox D10
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: HOX4; HOX4D; HOX4E; Hox-4.4
Summary: 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]
Expression: Biased expression in endometrium (RPKM 21.4), kidney (RPKM 9.2) and 4 other tissues
Orthologs: mouse
Gene size: 3160bp
Exon count: 2