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Gene information for HOXD13 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID3239
Official gene symbolHOXD13
Full namehomeobox D13
Aliases,BDE,BDSD,HOX4I,SPD,
Gene summaryThis 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, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq]
LocationChromosome: 2   Locus: 2q31.1
Gene position176957532 - 176960666  Map Viewer
Gene orientationplus
Gene size3135 bp
Gene sequence
OMIM ID142989