Phenotypes for mgb Myocd MGI:6450805 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Myocd^tm1.1Msp/mgb
Genetic Background	involves: 129/Sv * FVB/N

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
mgb mutation (0 available); any mgb mutation (0 available)
Myocd^tm1.1Msp mutation (0 available); any Myocd mutation (55 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

postnatal lethality, complete penetrance ( J:283803 )

• die within 1 week of birth

cardiovascular system

patent ductus arteriosus ( J:283803 )

• in newborns

renal/urinary system

abnormal urinary bladder morphology ( J:283803 )

• thin bladder wall

distended urinary bladder ( J:283803 )

• grossly dilated bladders

cellular

patent ductus arteriosus ( J:283803 )

• in newborns

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
congenital megabladder		DOID:0112014	OMIM:618719	J:283803

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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