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Symbol
Name
ID
Acvr1
activin A receptor, type 1
MGI:87911
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Widely spaced teeth
Disease(s) Associated with ACVR1
fibrodysplasia ossificans progressiva

Mouse Phenotypes
abnormal pharyngeal arch artery morphology
abnormal sixth pharyngeal arch artery morphology
abnormal third pharyngeal arch artery morphology
abnormal Meckel's cartilage morphology
large anterior fontanelle
abnormal frontal bone squamous part morphology
abnormal mandibular fossa morphology
absent retrotympanic process
small temporal bone squamous part
absent temporal bone zygomatic process
abnormal zygomatic arch morphology
abnormal mandible morphology
small mandibular coronoid process
absent mandibular symphysis
absent temporomandibular joint
mandible hypoplasia
short mandible
absent zygomatic bone
abnormal malleus morphology
short malleus manubrium
abnormal palatal shelf elevation
delayed palatal shelf elevation
cleft secondary palate
shortened head
Availability Mouse Genotype
Acvr1tm1Vk/Acvr1tm1.1Vk
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (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
04/09/2024
MGI 6.23
The Jackson Laboratory