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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cryba1
crystallin, beta A1
MGI:88518
22 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cryba1Po1/Cryba1+
C3HeB/FeJ
total cataracts J:58912
Cryba1Po1/Cryba1Po1
C3HeB/FeJ
microphthalmia J:58912
total cataracts J:58912
Cryba1tm1.1Dbsa/Cryba1tm1.1Dbsa
Tg(BEST1-cre)1Jdun/0
involves: 129S6/SvEvTac * C57BL/6
abnormal autophagy J:215838
abnormal lysosome morphology J:215838
abnormal lysosome physiology J:215838
abnormal retinal pigment epithelium morphology J:215531, J:215838
abnormal retinal pigmentation J:215838
decreased a wave amplitude J:215838
decreased b wave amplitude J:215838
gliosis J:215531
lysosomal protein accumulation J:215531
retinal degeneration J:215531
Cryba1tm1a(EUCOMM)Hmgu/Cryba1tm1a(EUCOMM)Hmgu
involves: C57BL/6J * C57BL/6N
abnormal autophagy J:235696
abnormal calcium ion homeostasis J:235696
abnormal cell cytoskeleton morphology J:235696
abnormal enzyme/coenzyme activity J:235696
abnormal lens epithelium morphology J:235696
abnormal lens fiber morphology J:235696
abnormal lens morphology J:235696
abnormal lysosome morphology J:235696
abnormal lysosome physiology J:235696
increased mitochondria number J:235696
microphthalmia J:235696
nuclear cataracts J:235696
persistent hyaloid artery J:235696
small lens J:235696

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/13/2017
MGI 6.11
The Jackson Laboratory