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| Nomenclature |
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Symbol:
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Hps5ru2-mr
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Name:
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Hermansky-Pudlak syndrome 5 homolog (human);
maroon
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MGI ID: |
MGI:1856146 |
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Synonyms: |
mr |
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Gene:
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Hps5
Location:
Chr7:46760466-46796064 bp, - strand
Genetic Position: Chr7,
30.56 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: | |
Spontaneous |
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Mutation: | |
Undefined |
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Mutation details: A spontaneous mutation that arose in a "lactation" stock. Maroon was shown to be allelic to ru2 by complementation testing.
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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 Hps5 Mutation:
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57 strains or lines available |
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| References |
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Original: |
J:15003
Bateman N,
"Maroon - allele of silver?"
Mouse News Lett 1957;16():7
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All: |
7 reference(s)
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Analysis Tools
