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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Crx
cone-rod homeobox
MGI:1194883
58 phenotypes from 9 alleles in 10 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Crxem1(IMPC)Ccpcz/Crxem1(IMPC)Ccpcz
C57BL/6N-Crxem1(IMPC)Ccpcz/Ccpcz
abnormal heart morphology J:211773
abnormal retina morphology J:211773
abnormal seminal vesicle morphology J:211773
abnormal skin morphology J:211773
abnormal testis morphology J:211773
abnormal thymus morphology J:211773
abnormal urinary bladder morphology J:211773
decreased exploration in new environment J:211773
enlarged heart J:211773
enlarged thymus J:211773
enlarged urinary bladder J:211773
increased fasting circulating glucose level J:211773
increased NK cell number J:211773
short tibia J:211773
small testis J:211773
small thymus J:211773
Crxem1Smgc/Crx+
C57BL/6J-Crxem1Smgc
abnormal cone electrophysiology J:343281
abnormal retina progenitor cell morphology J:343281
abnormal rod electrophysiology J:343281
decreased a-wave amplitude J:343281
decreased b-wave amplitude J:343281
disorganized retina outer nuclear layer J:343281
normal vision/eye phenotype J:343281
Crxem1Smgc/Crxem1Smgc
C57BL/6J-Crxem1Smgc
abnormal retina progenitor cell morphology J:343281
absent photoreceptor outer segment J:343281
absent visual evoked potential J:343281
binocular blindness J:343281
disorganized retina outer nuclear layer J:343281
normal vision/eye phenotype J:343281
Crxem2Smgc/Crx+
C57BL/6J-Crxem2Smgc
absent photoreceptor outer segment J:343281
absent visual evoked potential J:343281
binocular blindness J:343281
disorganized retina outer nuclear layer J:343281
vision/eye phenotype J:343281
Crxem2Smgc/Crxem2Smgc
C57BL/6J-Crxem2Smgc
absent photoreceptor outer segment J:343281
absent visual evoked potential J:343281
binocular blindness J:343281
disorganized retina outer nuclear layer J:343281
vision/eye phenotype J:343281
CrxRip/Crx+
C57BL/6J-CrxRip
abnormal blood circulation J:203337
abnormal cone electrophysiology J:203337
abnormal retina blood vessel morphology J:203337
abnormal retina photoreceptor morphology J:203337
abnormal rod electrophysiology J:203337
absent photoreceptor outer segment J:203337
blindness J:203337
retina spots J:203337
short photoreceptor inner segment J:203337
normal vision/eye phenotype J:203337
CrxRip/CrxRip
C57BL/6J-CrxRip
abnormal retina photoreceptor layer morphology J:203337
abnormal retina photoreceptor morphology J:203337
Crxtm1.1Smgc/Crx+
B6.129X1(CBA)-Crxtm1.1Smgc
abnormal electroretinogram waveform feature J:211011
abnormal retina cone cell morphology J:211011
abnormal retina layer morphology J:211011
abnormal retina outer nuclear layer morphology J:211011
abnormal retina outer nuclear layer thickness J:211011
decreased a-wave amplitude J:211011
decreased b-wave amplitude J:211011
decreased retina cone cell number J:211011
short retina rod cell outer segment J:211011
Crxtm1.1Smgc/Crxtm1.1Smgc
B6.129X1(CBA)-Crxtm1.1Smgc
abnormal electroretinogram waveform feature J:211011
abnormal retina layer morphology J:211011
absent photoreceptor outer segment J:211011
retina outer nuclear layer degeneration J:211011
normal vision/eye phenotype J:211011
Crxtm1Clc/Crx+
involves: 129S6/SvEvTac
abnormal photoreceptor outer segment morphology J:58796
abnormal retina morphology J:58796
thin retina outer nuclear layer J:58796
Crxtm1Clc/Crxtm1Clc
involves: 129S6/SvEvTac
abnormal circadian behavior J:58796
abnormal cone electrophysiology J:58796
abnormal electroretinogram waveform feature J:211011
abnormal eye electrophysiology J:58796
abnormal photoreceptor inner segment morphology J:95886
abnormal photoreceptor outer segment morphology J:95886
abnormal retina bipolar cell morphology J:88825
abnormal retina cone bipolar cell morphology J:88825
abnormal retina horizontal cell morphology J:88825
abnormal retina layer morphology J:211011
abnormal retina morphology J:58796
abnormal retina outer plexiform layer morphology J:95886
abnormal retina photoreceptor layer morphology J:58796
abnormal retina photoreceptor morphology J:58796
abnormal retina rod bipolar cell morphology J:88825
abnormal rod electrophysiology J:58796
absent photoreceptor outer segment J:58796, J:211011
delayed circadian behavior phase J:58796
retina outer nuclear layer degeneration J:211011
thin retina outer nuclear layer J:58796, J:88825
normal vision/eye phenotype J:211011
Crxtm1Clc/Crxtm1Clc
involves: 129S6/SvEvTac * C57BL/6J
abnormal retina photoreceptor layer morphology J:203337
Crxtm1Smgc/Crx+
involves: 129X1/SvJ
abnormal electroretinogram waveform feature J:211011
abnormal retina cone cell morphology J:211011
short retina rod cell outer segment J:211011
normal vision/eye phenotype J:211011
Crxtm2.1Smgc/Crx+
B6.129X1(CBA)-Crxtm2.1Smgc
abnormal retina cone cell morphology J:211011
decreased b-wave amplitude J:211011
normal vision/eye phenotype J:211011
Crxtm2.1Smgc/Crxtm2.1Smgc
B6.129X1(CBA)-Crxtm2.1Smgc
abnormal electroretinogram waveform feature J:211011
abnormal retina layer morphology J:211011
absent photoreceptor outer segment J:211011
retina outer nuclear layer degeneration J:211011
normal vision/eye phenotype J:211011
Crxtvrm65/Crxtvrm65
C57BL/6J-Crxtvrm65/J
abnormal ocular fundus morphology J:166679
abnormal retina pigmentation J:166679
absent photoreceptor inner segment J:166679
absent photoreceptor outer segment J:166679
retina outer nuclear layer degeneration J:166679
retina photoreceptor degeneration J:166679
thin retina outer plexiform layer J:166679

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
04/30/2024
MGI 6.23
The Jackson Laboratory