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Symbol
Name
ID

Slc7a14
solute carrier family 7 (cationic amino acid transporter, y+ system), member 14
MGI:3040688

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Bone spicule pigmentation of the retina	Retinal atrophy	Rod-cone dystrophy	Nyctalopia	Reduced visual acuity	Visual field defect
Disease(s) Associated with SLC7A14
retinitis pigmentosa 68

Mouse Phenotypes		short photoreceptor outer segment	thin retina outer nuclear layer	decreased total retina thickness	abnormal eye electrophysiology	abnormal rod electrophysiology
Availability	Mouse Genotype	short photoreceptor outer segment	thin retina outer nuclear layer	decreased total retina thickness	abnormal eye electrophysiology	abnormal rod electrophysiology
	Slc7a14^em1Jin/Slc7a14^em1Jin
	Slc7a14^em1Jqu/Slc7a14^em1Jqu

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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