BMPR1B wt Allele

Human BMPR1B wild-type allele is located within 4q22-q24 and is approximately 397 kb in length. This allele, which encodes bone morphogenetic protein receptor type IB protein, plays a role in the regulation of signaling. Mutations in the gene are associated with both acromesomelic chondrodysplasia with genital anomalies and brachydactyly types A2 and C. (NCI Thesaurus)

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BMPR1B Gene

This gene is involved in the mediation of signal transduction.

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…

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.