BMPR1B Chromosome 4
Bone morphogenetic protein receptor type 1B
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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 |