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| Nomenclature |
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Symbol:
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Tyrc-25H
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Name:
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tyrosinase;
albino 25 Harwell
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MGI ID: |
MGI:1856306 |
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Synonyms: |
c25H, Del(7)c-25H |
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Gene:
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Tyr
Location:
Chr7:87427405-87493411 bp, - strand
Genetic Position: Chr7,
49.01 cM
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Mutation
origin |
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Strain of Origin:
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Not Specified
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Intergenic deletion |
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Mutation details: This allele comprises a cytologically visible intergenic deletion estimated to be less than 6 cM. Minimally Tyr and Mod2 are deleted. (J:5520)
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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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| 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:5435
Gluecksohn-Waelsch S et al.,
"Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase."
Proc Natl Acad Sci U S A 1974 Mar;71(3):825-9
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All: |
6 reference(s)
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Analysis Tools
