VARIANT: 659v1
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Entry
659v1 Variant
Name
BMPR2 mutation
Type
Loss of function
Gene
BMPR2
bone morphogenetic protein receptor type 2 [KO:
K04671
]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar:
600799
Network
nt06507
TGFB signaling
Disease
H01619
Primary pulmonary hypertension
Reference
PMID:
31406341
Authors
Southgate L, Machado RD, Graf S, Morrell NW
Title
Molecular genetic framework underlying pulmonary arterial hypertension.
Journal
Nat Rev Cardiol 17:85-95 (2020)
DOI:
10.1038/s41569-019-0242-x
Reference
PMID:
30545973
Authors
Morrell NW, Aldred MA, Chung WK, Elliott CG, Nichols WC, Soubrier F, Trembath RC, Loyd JE
Title
Genetics and genomics of pulmonary arterial hypertension.
Journal
Eur Respir J 53:1801899 (2019)
DOI:
10.1183/13993003.01899-2018
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