Tyrc-26DVT
Radiation induced Allele Detail
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| Nomenclature |
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Symbol:
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Tyrc-26DVT
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Name:
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tyrosinase;
albino deletion 26DVT, Oak Ridge
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MGI ID: |
MGI:2153742 |
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Synonyms: |
c26DVT, cFp1, Df(c Mod-2 sh-1)26DVT, Tyrc-49R, Tyrc-Fp1 |
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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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(101/Rl x C3H/Rl)F1
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Deletion |
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Mutation details: This multi-locus deletion, induced by X-ray irradiation of a male mouse, encompasses G-bands 7D3-7E3 and includes, proximally, Fah (fumarylacetoacetate hydrolase) and distally, Aqp11 (aquaporin 11; formerly sjds). The deletion is flanked proximally by Mesdc2, mesoderm development candidate 2, and distally by Hbb, the hemoglobin beta chain complex. (J:54592, J:100221)
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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:23420
Russell LB et al.,
"Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies."
Genetics 1982 Mar;100(3):427-53
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All: |
13 reference(s)
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Analysis Tools
