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Symbol
Name
ID
Bmpr1a
bone morphogenetic protein receptor, type 1A
MGI:1338938
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Clubbing
Disease(s) Associated with BMPR1A
juvenile polyposis syndrome

Mouse Phenotypes
skeleton phenotype
abnormal osteoclast differentiation
abnormal neurocranium morphology
large anterior fontanelle
small frontal bone
enlarged parietal bone
abnormal tooth morphology
abnormal tooth development
absent teeth
abnormal nasal bone morphology
decreased osteoclast cell number
abnormal osteoclast physiology
osteoarthritis
abnormal skeleton morphology
abnormal long bone epiphysis morphology
decreased length of long bones
abnormal thoracic cage shape
small thoracic cage
abnormal bone structure
increased bone mass
osteosclerosis
abnormal cartilage development
abnormal articular cartilage morphology
abnormal synovial joint membrane morphology
fused joints
abnormal skeleton development
chondrodystrophy
abnormal skeleton physiology
abnormal bone ossification
increased bone mineralization
decreased bone ossification
delayed bone ossification
decreased joint mobility
Availability Mouse Genotype
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr
Tg(Col2a1-cre)1Bhr/?  (conditional)
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr
Tg(Col1a1-cre/Esr1*)1Mis/0  (conditional)
Bmpr1atm2Bhr/Bmpr1atm2Bhr
Tg(KRT14-cre)40Smr/?  (conditional)
Bmpr1atm2Bhr/Bmpr1atm2Bhr
Tg(KRT14-cre)43Smr/?  (conditional)
Bmpr1atm2Bhr/Bmpr1atm2Bhr
Tg(KRT14-cre)52Smr/0  (conditional)
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr
Tg(CAG-cre/Esr1*)5Amc/0  (conditional)
*
Bmpr1atm2.1Bhr/Bmpr1atm2.2Bhr
Tg(Gdf5-cre,-ALPP)1Kng/0  (conditional)
Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0
Tg(Mpz-cre)94Imeg/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/14/2024
MGI 6.23
The Jackson Laboratory