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Phenotypes Associated with This Genotype
Genotype
MGI:3767206
Allelic
Composition		 Ocrltm2Nbm/Y
Genetic
Background		 either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ocrltm2Nbm mutation (0 available); any Ocrl mutation (9 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
mortality/aging ( J:47884 )
N
• no prenatal mortality
• no evidence of perinatal morbidity

reproductive system
reproductive system phenotype ( J:47884 )
N
• normal development and fertility

vision/eye
vision/eye phenotype ( J:47884 )
N
• no congenital cataracts

homeostasis/metabolism
homeostasis/metabolism phenotype ( J:47884 )
N
• phosphate excretion is normal

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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Funding Information
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory