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| Nomenclature |
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Symbol:
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Hbath-J
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Name:
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hemoglobin alpha chain complex;
alpha thalassemia Jackson
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MGI ID: |
MGI:1858115 |
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Synonyms: |
alphaMD |
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Gene:
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Hba
Location:
unknown
Genetic Position: Chr11,
cytoband A
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Mutation
origin |
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Strain of Origin:
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C57BL/6J x Triethyllenemelamine-treated male
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Mutation
description |
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Allele
Type: | |
Chemically induced (other) |
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Mutation: | |
Intergenic deletion |
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Mutation details: This mutation was shown to be a deletion that included the Hba-x, Hba-a1 and Hba-a2 genes (J:32654). The Mpg, Rhbdf1 and Phg genes are also included in the deletion region (J:29665). (J:29665, J:32654)
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Inheritance: | |
Codominant |
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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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Notes |
The mutation was induced in a male mouse by triethyllenemelamine.
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| References |
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Original: |
J:45721
Whitney JB et al.,
"New mutants and biochemical variants: Alpha thalassemia"
Mouse News Lett 1978;58():47-48
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All: |
11 reference(s)
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Analysis Tools
