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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 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
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+

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
05/21/2024
MGI 6.23
The Jackson Laboratory