Phenotypes for Ocrl MGI:2668816 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Ocrl^tm1Nbm/Ocrl^tm1Nbm
Genetic Background	either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ocrl^tm1Nbm mutation (1 available); any Ocrl mutation (9 available)

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

normal phenotype

no abnormal phenotype detected ( J:47884 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
NOT	oculocerebrorenal syndrome	DOID:1056	OMIM:309000	J:47884

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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