Mouse Genome Informatics
hm
    Ocrltm1Nbm/Ocrltm1Nbm
either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       
normal phenotype

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