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Symbol
Name
ID

Mfsd8
major facilitator superfamily domain containing 8
MGI:1919425

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Pigmentary retinopathy	Retinopathy	Blindness	Visual loss
Disease(s) Associated with MFSD8
neuronal ceroid lipofuscinosis 7

Mouse Phenotypes		impaired pupillary reflex	abnormal retina vasculature morphology	retina photoreceptor degeneration	abnormal retina morphology
Availability	Mouse Genotype	impaired pupillary reflex	abnormal retina vasculature morphology	retina photoreceptor degeneration	abnormal retina morphology
	Mfsd8^{tm1a(EUCOMM)Hmgu}/Mfsd8^{tm1a(EUCOMM)Hmgu}
	Mfsd8^{tm1b(EUCOMM)Hmgu}/Mfsd8^{tm1b(EUCOMM)Hmgu}

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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