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BMP2 wt Allele

Known as: Bone Morphogenetic Protein 2A Gene, BMP2A, Bone Morphogenetic Protein 2 wt Allele 
Human BMP2 wild-type allele is located within 20p12 and is approximately 11 kb in length. This allele, which encodes bone morphogenetic protein 2, is… 
National Institutes of Health

Related topics

Related topics

11 relations
20p12ALK PathwayCell Differentiation processCell Proliferation Regulatory Process
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Papers overview

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2015
2015
Comparative analysis of zebrafish bone morphogenetic proteins 2, 4 and 16: molecular and evolutionary perspectives
BMP2, BMP4 and BMP16 form a subfamily of bone morphogenetic proteins acting as pleiotropic growth factors during development and… 
2015
2015
Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1
Brachydactyly type A1 is an autosomal dominant disorder primarily characterized by hypoplasia/aplasia of the middle phalanges of… 
2014
2014
Identification of Duplication Downstream of BMP2 in a Chinese Family with Brachydactyly Type A2 (BDA2)
Brachydactyly type A2 (BDA2, MIM 112600) is characterized by the deviation and shortening of the middle phalange of the index… 
2012
2012
Essential roles of zebrafish bmp2a, fgf10, and fgf24 in the specification of the ventral pancreas
In vertebrates, pancreas and liver arise from bipotential progenitors located in the endoderm. At early stages, BMP and FGF are… 
Highly Cited
2009
Highly Cited
2009
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2.
Highly Cited
2008
Highly Cited
2008
Mypt1-mediated spatial positioning of Bmp2-producing cells is essential for liver organogenesis
Mesodermal tissues produce various inductive signals essential for morphogenesis of endodermal organs. However, little is known… 
2006
2006
Conservation and divergence of Bmp2a, Bmp2b, and Bmp4 expression patterns within and between dentitions of teleost fishes
SUMMARY The diversity of tooth location in teleost fishes provides an excellent system for comparing genetic divergence between… 
Highly Cited
2006
Highly Cited
2006
A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2
Heterozygous missense mutations in the serine-threonine kinase receptor BMPR1B result typically in brachydactyly type A2 (BDA2… 
Review
2006
Review
2006
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2
Background: Brachydactyly type A2 (OMIM 112600) is characterised by hypoplasia/aplasia of the second middle phalanx of the index… 
Highly Cited
2004
Highly Cited
2004
Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2
The brachydactylies are a group of inherited disorders of the hands characterized by shortened digits. Mutations in the tyrosine… 
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