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Proper Citation: RRID:MGI:5630823
Description: Allele Detail: Targeted This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Targeted This is a legacy resource.
Phenotype: abnormal coronary sinus connection, persistent dorsal ophthalmic artery, abnormal Mullerian duct morphology, embryo tumor, abnormal optic cup morphology, muscular ventricular septal defect, absent hypoglossal canal, thin hypoglossal nerve, absent hypoglossal nerve, abnormal hypoglossal nerve topology, subcutaneous edema, enlarged liver sinusoidal spaces, hemopericardium, preweaning lethality, incomplete penetrance, abnormal intestine placement, absent stapedial artery, abnormal eye muscle morphology, biliary cyst, arteriovenous malformation, double outlet right ventricle, abnormal ductus venosus valve topology, abnormal ductus venosus valve morphology, absent ductus venosus valve, trigeminal neuroma, overriding aortic valve, perimembraneous ventricular septal defect, abnormal infrahyoid muscle connection, abnormal lens epithelium morphology, abnormal vein morphology, abnormal inferior vena cava morphology, multiple persisting craniopharyngeal ducts, blood in lymph vessels, heterochrony, abnormal atrioventricular cushion morphology, short snout, small superior cervical ganglion, abnormal forebrain morphology, absent superior cervical ganglion, abnormal hypoglossal canal morphology, small hypoglossal canal
Affected Gene: Actn4
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No rating or validation information has been found for Actn4tm1a(EUCOMM)Wtsi/Actn4tm1a(EUCOMM)Wtsi.
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Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI
