HOXD13
Sign in to saveAlso known as BDE, BDSD, HOX4I, SPD, SPD1, homeobox D13
Homeobox protein Hox-D13 is a protein that in humans is encoded by the HOXD13 gene. 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.
Gene data
HOXD13- Name
- homeobox D13
- Type
- protein-coding
- Position
- 176,092,690–176,096,240 (+)
- Aliases
- BDE, BDSD, HOX4I, SPD, SPD1
- Ensembl
- ENSG00000128714
- RefSeq RNA
- NM_000523.4, XM_011511068.3, XM_011511069.3
- RefSeq protein
- NP_000514.2, XP_011509370.1, XP_011509371.1
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, 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, Jul 2008].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
homeobox D13
- Symbol
- HOXD13
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 2:176,092,690-176,096,240
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
~2 min read
Encyclopedic overview
5 sectionsContents
- Clinical significance
- See also
- References
- Further reading
- External links
Homeobox protein Hox-D13 is a protein that in humans is encoded by the HOXD13 gene. 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, located on different chromosomes, consisting of 9–11 genes arranged in tandem. HOXD13 is the first of several 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. The product of the mouse Hoxd13 gene plays a role in axial skeleton development and forelimb morphogenesis.
Excerpted from Wikipedia’s “HOXD13” article, available under the CC BY-SA 4.0 licence.