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| Nomenclature |
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Symbol:
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Catb
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Name:
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catalase;
acatalasemia
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MGI ID: |
MGI:3053604 |
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Synonyms: |
Csb, M1 |
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Gene:
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Cat
Location:
Chr2:103453849-103485160 bp, - strand
Genetic Position: Chr2,
54.43 cM
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Mutation
origin |
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Strain of Origin:
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(101 x C3H)F1
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Nucleotide substitutions |
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Mutation details: This allele corresponds to a mutation located in the first alpha helix in the amino terminal arm of the catalase subunit. The substitution of G to T results in an amino acid substitution that replaces glutamine with histidine at position 11. (J:10926)
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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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| References |
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Original: |
J:5015
Feinstein RN et al.,
"Acatalasemic and hypocatalasemic mouse mutants."
Genetics 1966 May;53(5):923-33
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All: |
18 reference(s)
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Analysis Tools
