Phenotypes for Ocrl MGI:2668816 MGI Mouse

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24