Phenotypes Associated with This Genotype

Genotype
MGI:2668816

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

• ♀: 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