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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Crb1
crumbs family member 1, photoreceptor morphogenesis associated
MGI:2136343
25 phenotypes from 8 alleles in 9 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Crb1em1Jnk/Crb1em1Jnk
involves: C57BL/6J * SJL
abnormal retina outer limiting membrane morphology J:293375
Crb1em2Jnk/Crb1em2Jnk
involves: C57BL/6J * SJL
abnormal retina outer limiting membrane morphology J:293375
Crb1em3Jnk/Crb1em3Jnk
involves: C57BL/6J * SJL
abnormal photoreceptor inner segment morphology J:293375
abnormal retina outer limiting membrane morphology J:293375
retina photoreceptor degeneration J:293375
Crb1em4Jnk/Crb1em4Jnk
involves: C57BL/6J * SJL
abnormal photoreceptor inner segment morphology J:293375
abnormal retina outer limiting membrane morphology J:293375
retina photoreceptor degeneration J:293375
Crb1rd8+em1Mvw/Crb1rd8
C57BL/6NJ-Crb1rd8+em1Mvw
normal vision/eye phenotype J:206789
Crb1rd8/Crb1rd8
B6.Cg-Crb1rd8
normal vision/eye phenotype J:85459
Crb1rd8/Crb1rd8
B6.Cg-Crb1rd8 Jak3+/Boc
abnormal retina morphology J:265859
abnormal retina pigment epithelium morphology J:265859
abnormal retina pigmentation J:265859
abnormal retina vasculature morphology J:265859
retina neovascularization J:265859
retina spots J:265859
Crb1rd8/Crb1rd8
involves: C3HfB6/Ga * C57BL/6 * CAST/EiJ
abnormal retina morphology J:85459
Crb1rd8/Crb1rd8
involves: C57BL/6N
abnormal retina pigment epithelium morphology J:182353
retina degeneration J:182353
Crb1rd8/Crb1rd8
STOCK Crb1rd8/J
abnormal Muller cell morphology J:85459
abnormal ocular fundus morphology J:85459
abnormal photoreceptor inner segment morphology J:85459
abnormal retina morphology J:85459
abnormal retina outer limiting membrane morphology J:85459
abnormal retina photoreceptor morphology J:85459
decreased retina photoreceptor cell number J:85459
photoreceptor outer segment degeneration J:85459
short photoreceptor inner segment J:85459
short photoreceptor outer segment J:85459
thin retina outer nuclear layer J:85459
Crb1tm1Wij/Crb1tm1Wij
involves: 129P2/OlaHsd * C57BL/6
abnormal Muller cell morphology J:92068
abnormal retina photoreceptor morphology J:92068
photosensitivity J:92068
retina degeneration J:92068
Crb1tm1Wij/Crb1tm2Wij
involves: 129P2/OlaHsd * C57BL/6
abnormal retina inner nuclear layer morphology J:117415
abnormal retina morphology J:117415
abnormal retina outer nuclear layer morphology J:117415
abnormal retina photoreceptor layer morphology J:117415
retina fold J:117415
thin retina outer nuclear layer J:117415
Crb1tm2Wij/Crb1tm2Wij
either: B6.129P2-Crb1tm2Wij or (involves: 129P2/OlaHsd * C57BL/6)
preweaning lethality, complete penetrance J:117415

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
04/09/2024
MGI 6.23
The Jackson Laboratory