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Symbol
Name
ID
Crx
cone-rod homeobox
MGI:1194883
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Photophobia
Disease(s) Associated with CRX
Leber congenital amaurosis 7

Mouse Phenotypes
decreased retinal cone cell number
abnormal horizontal cell morphology
abnormal retinal bipolar cell morphology
abnormal retinal cone bipolar cell morphology
abnormal retinal rod bipolar cell morphology
abnormal retinal photoreceptor morphology
abnormal photoreceptor inner segment morphology
absent photoreceptor inner segment
short photoreceptor inner segment
abnormal photoreceptor outer segment morphology
absent photoreceptor outer segment
abnormal retinal rod cell outer segment morphology
abnormal retinal cone cell morphology
retinal photoreceptor degeneration
Availability Mouse Genotype
CrxRip/CrxRip
Crxtm1.1Smgc/Crxtm1.1Smgc
Crxtm1Clc/Crxtm1Clc
Crxtm2.1Smgc/Crxtm2.1Smgc
Crxtvrm65/Crxtvrm65
CrxRip/Crx+
Crxtm1.1Smgc/Crx+
Crxtm1Clc/Crx+
Crxtm1Smgc/Crx+
Crxtm2.1Smgc/Crx+

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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last database update
03/24/2020
MGI 6.15
The Jackson Laboratory