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| Nomenclature |
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Symbol:
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CrygbS11R
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Name:
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crystallin, gamma B;
S11R
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MGI ID: |
MGI:3777015 |
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Gene:
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Crygb
Location:
Chr1:65080228-65082267 bp, - strand
Genetic Position: Chr1,
32.82 cM
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Mutation
origin |
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Single point mutation |
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Mutation details: Mice possess an A to C point mutation in codon 11 that results in the amino acid substitution of arginine for serine at position 11 (S11R). (J:132502)
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Inheritance: | |
Recessive |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Crygb Mutation:
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3 strains or lines available |
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| References |
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Original: |
J:132502
Li L et al.,
"Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation."
Invest Ophthalmol Vis Sci 2008 Jan;49(1):304-9
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All: |
2 reference(s)
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Analysis Tools
