Symbol Name ID |
Crx
cone-rod homeobox MGI:1194883 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Disease(s) Associated with CRX | |
Leber congenital amaurosis 7 |
Mouse Phenotypes | decreased retina cone cell number |
abnormal retina bipolar cell morphology |
abnormal retina cone bipolar cell morphology |
abnormal retina rod bipolar cell morphology |
abnormal retina horizontal cell morphology |
abnormal retina photoreceptor morphology |
abnormal photoreceptor inner segment morphology |
absent photoreceptor inner segment |
short photoreceptor inner segment |
abnormal photoreceptor outer segment morphology |
absent photoreceptor outer segment |
short retina rod cell outer segment |
abnormal retina cone cell morphology |
retina photoreceptor degeneration |
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Availability | Mouse Genotype | ||||||||||||||
Crxem1Smgc/Crxem1Smgc | |||||||||||||||
Crxem2Smgc/Crxem2Smgc | |||||||||||||||
CrxRip/CrxRip | |||||||||||||||
Crxtm1.1Smgc/Crxtm1.1Smgc | |||||||||||||||
Crxtm1Clc/Crxtm1Clc | |||||||||||||||
Crxtm2.1Smgc/Crxtm2.1Smgc | |||||||||||||||
Crxtvrm65/Crxtvrm65 | |||||||||||||||
Crxem2Smgc/Crx+ | |||||||||||||||
CrxRip/Crx+ | |||||||||||||||
Crxtm1.1Smgc/Crx+ | |||||||||||||||
Crxtm1Clc/Crx+ | |||||||||||||||
Crxtm1Smgc/Crx+ | |||||||||||||||
Crxtm2.1Smgc/Crx+ |
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 05/21/2024 MGI 6.23 |
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