Phenotypes Associated with This Genotype

Genotype
MGI:6272871

• Allelic Composition: Nmnat1^tm1Ruch/Nmnat1^tm1Ruch
• Genetic Background: involves: 129S7/SvEvBrd

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

normal phenotype

no abnormal phenotype detected ( J:267630 )

• mice are viable and fertile, show no retinal degeneration and normal retinal function, and mice subjected to strong white light for 4 hours show unaffected retinal morphology 2 weeks after exposure to the light damage

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
NOT	Leber congenital amaurosis 9	DOID:0110005	OMIM:608553	J:267630