Ocrl^tm1Nbm/Ocrl^tm1Nbm
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

no abnormal phenotype detected ( J:47884 )

(J:47884)

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