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HOXD13

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Anti-HOXD13 Recombinant Antibody Products

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For Research Use Only. Not For Clinical Use.


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.
Protein class

Cancer-related genes, Disease related genes, Human disease related genes, Transcription factors

Predicted location

Intracellular

Single cell type specificity

Cell type enhanced (Enteroendocrine cells, Basal prostatic cells, Undifferentiated cells, Intestinal goblet cells, Urothelial cells, Prostatic glandular cells, Paneth cells, Distal enterocytes)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (HAP1, HEK93, HL-60, JURKAT, NB-4)

Molecular function

Developmental protein, DNA-binding

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