Phenotypes Associated with This Genotype

Genotype
MGI:5490868

• Allelic Composition: Rho^{tm4.1(RHO*/EGFP)Jhw}/Rho⁺
• Genetic Background: B6.129S7-Rho^{tm4.1(RHO*/EGFP)Jhw}

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

vision/eye

vision/eye phenotype ( J:196863 )

N • responses of eyes to flashes of light of varying intensities at 1 month of age are similar to controls

abnormal retina morphology ( J:196863 )

• mislocalization of mutant rhodopsin to the inner segments and outer nuclear layer of the retina

retina degeneration ( J:196863 )

• very slow, similar to mice heterozygous for Rho^tm2Jhw

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
retinitis pigmentosa 4		DOID:0110372	OMIM:613731	J:196863