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Mouse Models of Lowe Oculocerebrorenal Syndrome; OCRL
Mouse Models All mouse models of Lowe Oculocerebrorenal Syndrome; OCRL (OMIM ID: 309000)

        Allelic Composition Genetic Background Reference Phenotypes
      Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Tg(INPP5B)CNbm/0
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N J:185879 View
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Y
Tg(INPP5B)CNbm/0
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N J:185879 View
Disease phenotype
not observed
No similarity to the expected human disease phenotype was found.

        Allelic Composition Genetic Background Reference Phenotypes
NOT Models     Ocrltm1Nbm/Ocrltm1Nbm either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss) J:47884 View

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
08/12/2014
MGI 5.19
The Jackson Laboratory