Symbol Name ID |
Crb2
crumbs family member 2 MGI:2679260 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | vision/eye phenotype |
abnormal retina blood vessel morphology |
retina neovascularization |
abnormal Muller cell morphology |
decreased retina photoreceptor cell number |
abnormal retina bipolar cell morphology |
short retina cone cell outer segment |
short retina rod cell outer segment |
abnormal retina cone cell outer segment morphology |
abnormal retina cone cell morphology |
abnormal retina pigment epithelium morphology |
abnormal ocular fundus morphology |
abnormal retina morphology |
abnormal retina layer morphology |
abnormal retina neuronal layer morphology |
abnormal retina ganglion layer morphology |
abnormal retina outer nuclear layer morphology |
thin retina outer nuclear layer |
abnormal retina outer plexiform layer morphology |
abnormal retina photoreceptor layer morphology |
abnormal retina outer limiting membrane morphology |
increased susceptibility to age-related retinal degeneration |
retina fold |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||
Crb2tm1a(KOMP)Wtsi/Crb2+ | |||||||||||||||||||||||||||||
Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (conditional) |
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Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Crx-cre)1Tfur/0 (conditional) |
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Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Pdgfra-cre)1Clc/0 (conditional) |
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Crb2tm1.1Wij/Crb2tm1.1Wij (conditional) | |||||||||||||||||||||||||||||
Crb2tm1.1Wij/Crb2+ Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (conditional) |
* |
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 04/23/2024 MGI 6.23 |
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