HPGD wt Allele

Human HPGD wild-type allele is located within 4q34-q35 and is approximately 32 kb in length. This allele, which encodes 15-hydroxyprostaglandin dehydrogenase [NAD+] protein, plays a role in the regulation of prostaglandin metabolism. Mutation of the gene is associated with primary hypertrophic osteoathropathy autosomal recessive and cranioosteoarthropathy. (NCI Thesaurus)

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HPGD Gene

This gene is involved in prostaglandin metabolism.

HPCA wt Allele

Human HPCA wild-type allele is located within 1p35-p34.2 and is approximately 8 kb in length. This allele, which encodes neuron-specific calcium-binding protein…

HPCA Gene

This gene plays a role in signal transduction and is involved in the regulation of cytosolic calcium ion concentration.

HP wt Allele

Human HP wild-type allele is located in the vicinity of 16q22.1 and is approximately 6 kb in length. This allele, which encodes…

HP Gene

This gene plays a role in hemoglobin interactions and in the prevention of oxidative tissue damage.

HOXD13 wt Allele

Human HOXD13 wild-type allele is located in the vicinity of 2q31.1 and is approximately 3 kb in length. This allele, which encodes…