BMPR1B Chromosome 4

Bone morphogenetic protein receptor type 1B
33 variants 33 Health Risk

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What This Gene Does
This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]
Gene Info
Gene Group
"Type 1 receptor serine/threonine kinases|CD molecules"
Locus Type
gene with protein product
Location
4q22.3
Ensembl
ENSG00000138696
Associated Conditions (11)
Type A2 brachydactyly
Acromesomelic dysplasia 3
Inborn genetic diseases
Brachydactyly
Idiopathic pulmonary arterial hypertension
BMPR1B-related disorder
Brachydactyly type A1D
Pulmonary arterial hypertension
Acromesomelic dysplasia 2C
Hunter-Thompson type
Acromesomelic dysplasia 2B
Key Variants
RS1346115955
Conflicting classifications of pathogenicity
Type A2 brachydactyly, Acromesomelic dysplasia 3, Inborn genetic diseases
Health Risk
RS140047318
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Acromesomelic dysplasia 3
Health Risk
RS143885868
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
Health Risk
RS150974461
Conflicting classifications of pathogenicity
Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
Health Risk
RS186299744
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Brachydactyly type A1D
Health Risk
RS200083866
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
Health Risk
RS200198618
Conflicting classifications of pathogenicity
Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
Health Risk
RS200702974
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
Health Risk
RS35973133
Conflicting classifications of pathogenicity
Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
Health Risk
RS369609245
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
Health Risk
RS373000965
Conflicting classifications of pathogenicity
Type A2 brachydactyly, Acromesomelic dysplasia 3, Inborn genetic diseases
Health Risk
RS759423600
Conflicting classifications of pathogenicity
Acromesomelic dysplasia 3, Type A2 brachydactyly, BMPR1B-related disorder
Health Risk
All Variants (33)
RSID Category Clinical Significance Conditions
RS1346115955 Health Risk Conflicting classifications of pathogenicity Type A2 brachydactyly, Acromesomelic dysplasia 3, Inborn genetic diseases
RS140047318 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Acromesomelic dysplasia 3
RS143885868 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
RS150974461 Health Risk Conflicting classifications of pathogenicity Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS186299744 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Brachydactyly type A1D
RS200083866 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
RS200198618 Health Risk Conflicting classifications of pathogenicity Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS200702974 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
RS35973133 Health Risk Conflicting classifications of pathogenicity Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS369609245 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
RS373000965 Health Risk Conflicting classifications of pathogenicity Type A2 brachydactyly, Acromesomelic dysplasia 3, Inborn genetic diseases
RS759423600 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, BMPR1B-related disorder
RS773095683 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Inborn genetic diseases
RS773417270 Health Risk Conflicting classifications of pathogenicity Type A2 brachydactyly, Acromesomelic dysplasia 3, Inborn genetic diseases
RS775495653 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS775608689 Health Risk Conflicting classifications of pathogenicity Acromesomelic dysplasia 3, Type A2 brachydactyly, Acromesomelic dysplasia 3
RS778257341 Health Risk Conflicting classifications of pathogenicity Brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS1057521819 Health Risk Likely pathogenic
RS1177728492 Health Risk Likely pathogenic Acromesomelic dysplasia 3, Acromesomelic dysplasia 3
RS121434417 Health Risk Likely pathogenic Type A2 brachydactyly, Type A2 brachydactyly
RS121434419 Health Risk Likely pathogenic Type A2 brachydactyly, BMPR1B-related disorder, Type A2 brachydactyly
RS1733349358 Health Risk Likely pathogenic
RS1734835445 Health Risk Likely pathogenic Acromesomelic dysplasia 2C, Hunter-Thompson type, Acromesomelic dysplasia 2C
RS2530214673 Health Risk Likely pathogenic Type A2 brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS121434418 Health Risk Pathogenic Type A2 brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS1553941890 Health Risk Pathogenic Acromesomelic dysplasia 2B, Type A2 brachydactyly, Acromesomelic dysplasia 3
RS1560671891 Health Risk Pathogenic Type A2 brachydactyly, Acromesomelic dysplasia 3, Type A2 brachydactyly
RS745854387 Health Risk Pathogenic Acromesomelic dysplasia 3, Acromesomelic dysplasia 3
RS863223287 Health Risk Pathogenic Acromesomelic dysplasia 3, Acromesomelic dysplasia 3
RS863225041 Health Risk Pathogenic Acromesomelic dysplasia 3, Acromesomelic dysplasia 3
RS863225042 Health Risk Pathogenic Acromesomelic dysplasia 3, Acromesomelic dysplasia 3
RS869025613 Health Risk Pathogenic Brachydactyly type A1D, Brachydactyly type A1D
RS869025614 Health Risk Pathogenic Brachydactyly type A1D, Brachydactyly type A1D
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