Symbol Name ID |
Acvr1
activin A receptor, type 1 MGI:87911 |
Darker colors indicate more annotations |
Human Phenotypes | Limitation of neck motion |
Failure to thrive |
Disease(s) Associated with ACVR1 | ||
fibrodysplasia ossificans progressiva |
Mouse Phenotypes | enlarged heart |
abnormal palatal shelf elevation |
delayed palatal shelf elevation |
cleft secondary palate |
shortened head |
decreased embryo size |
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Availability | Mouse Genotype | ||||||
Acvr1tm1.1Vk/Acvr1tm1.1Vk | |||||||
Acvr1tm1Bhr/Acvr1tm1Bhr | |||||||
Acvr1tm1Enl/Acvr1tm1Enl | |||||||
Acvr1tm1Vk/Acvr1tm1.1Vk H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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 04/16/2024 MGI 6.23 |
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