BMPR1A wt Allele

Human BMPR1A wild-type allele is located in the vicinity of 10q22.3 and is approximately 169 kb in length. This allele, which encodes bone morphogenetic protein receptor type IA protein, is involved in signal transduction pertaining to bone morphogenesis. Germline mutations in the gene cause a subset of juvenile polyposis syndrome and Cowden syndrome. (NCI Thesaurus)

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BMPR1A Gene Mutation

A molecular genetic abnormality that refers to the mutation of the BMPR1A (bone morphogenetic protein receptor, type 1A) gene on chromosome…

BMPR1A Gene

This gene plays a role in the bone morphogenetic protein signaling pathway.

BMP8B wt Allele

Human BMP8B wild-type allele is located within 1p35-p32 and is approximately 31 kb in length. This allele, which encodes bone morphogenetic protein…

BMP8B Gene

This gene plays a role in calcium regulation and bone homeostasis. It is involved in cartilage and bone formation.

BMP7 wt Allele

Human BMP7 wild-type allele is located within 20q13 and is approximately 96 kb in length. This allele, which encodes bone morphogenetic protein…

BMP7 Gene

This gene is involved in calcium regulation and bone homeostasis. It also plays a role in the control of cellular development and…