Symbol Name ID |
Cln3
CLN3 lysosomal/endosomal transmembrane protein, battenin MGI:107537 |
Darker colors indicate more annotations |
Human Phenotypes | Cataract |
Optic atrophy |
Macular degeneration |
Retinal degeneration |
Rod-cone dystrophy |
Undetectable electroretinogram |
Reduced visual acuity |
Blindness |
Progressive visual loss |
Glaucoma |
Disease(s) Associated with CLN3 | ||||||||||
neuronal ceroid lipofuscinosis 3 |
Mouse Phenotypes | decreased retina photoreceptor cell number |
abnormal retina ganglion cell morphology |
abnormal retina morphology |
abnormal retina neuronal layer morphology |
abnormal retina ganglion layer morphology |
abnormal retina inner nuclear layer morphology |
retina degeneration |
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Availability | Mouse Genotype | |||||||
Cln3tm1.1Mem/Cln3tm1.1Mem | ||||||||
Cln3tm1Nbm/Cln3tm1Nbm |
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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last database update 04/16/2024 MGI 6.23 |
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