Phenotypes for mgb Myocd MGI:6450805 MGI Mouse

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 09/30/2025 MGI 6.24