Symbol Name ID |
Bmpr1a
bone morphogenetic protein receptor, type 1A MGI:1338938 |
Darker colors indicate more annotations |
Human Phenotypes | Hematochezia |
Disease(s) Associated with BMPR1A | |
juvenile polyposis syndrome |
Mouse Phenotypes | abnormal vascular development |
abnormal vascular branching morphogenesis |
abnormal vitelline vasculature morphology |
vascular smooth muscle hypoplasia |
abnormal vein morphology |
persistent truncus arteriosus |
absent atrioventricular cushions |
abnormal heart morphology |
abnormal mitral valve cusp morphology |
abnormal tricuspid valve morphology |
Ebstein's malformation of tricuspid valve |
abnormal tricuspid valve cusp morphology |
ventricular septal defect |
small heart |
pericardial effusion |
hemorrhage |
internal hemorrhage |
decreased cardiac muscle contractility |
abnormal fetal cardiomyocyte proliferation |
mitral valve regurgitation |
abnormal impulse conducting system conduction |
absent PR interval |
abnormal cardiomyocyte apoptosis |
|
Availability | Mouse Genotype | |||||||||||||||||||||||
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr Kdrtm1(cre)Sato/Kdr+ (conditional) |
||||||||||||||||||||||||
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Tg(GATA6-cre)#Jbeb/0 (conditional) |
||||||||||||||||||||||||
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Tg(Cga-cre)3Sac/0 (conditional) |
||||||||||||||||||||||||
Bmpr1atm2.1Bhr/Bmpr1atm2.2Bhr Isl1tm1(cre)Sev/Isl1+ (conditional) |
||||||||||||||||||||||||
Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|