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Phenotypes Associated with This Genotype
Genotype
MGI:2668816
Allelic
Composition
Ocrltm1Nbm/Ocrltm1Nbm
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:
Ocrltm1Nbm mutation (0 available); any Ocrl mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype

Mouse Models of Human Disease
OMIM ID Ref(s)
NOT Lowe Oculocerebrorenal Syndrome; OCRL 309000 J:47884


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/19/2016
MGI 6.04
The Jackson Laboratory