Symbol Name ID |
Acvr1
activin A receptor, type 1 MGI:87911 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Iris hypoperfusion |
Retinal vein occlusion |
Disease(s) Associated with ACVR1 | ||
exfoliation syndrome |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal pharyngeal arch artery morphology |
abnormal sixth pharyngeal arch artery morphology |
abnormal third pharyngeal arch artery morphology |
abnormal aortic arch morphology |
abnormal aortic arch and aortic arch branch attachment |
retroesophageal right subclavian artery |
abnormal brachiocephalic trunk morphology |
abnormal vascular endothelial cell differentiation |
abnormal cardiac epithelial to mesenchymal transition |
decreased cardiac neural crest cell number |
absent cardiac neural crest cells |
impaired cardiac neural crest cell differentiation |
abnormal cardiac outflow tract development |
conotruncal ridge hypoplasia |
persistent truncus arteriosus |
abnormal atrioventricular cushion morphology |
decreased atrioventricular cushion size |
abnormal atrioventricular valve development |
abnormal heart morphology |
atrial septal defect |
abnormal atrioventricular septum morphology |
ventricular septal defect |
enlarged heart |
increased heart right ventricle size |
cardiovascular shunt |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||
Acvr1tm1Vk/Acvr1tm1.1Vk H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Acvr1tm1Vk/Acvr1tm1.1Vk Tg(Tek-cre)12Flv/0 (conditional) |
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Acvr1tm1Vk/Acvr1tm1.1Vk Tg(Myh6-cre)2182Mds/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) |
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last database update 05/14/2024 MGI 6.23 |
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