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| Nomenclature |
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Symbol:
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Spta1sph-ha
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Name:
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spectrin alpha, erythrocytic 1;
hemolytic anemia
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MGI ID: |
MGI:1856181 |
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Synonyms: |
ha, sph1J, Sph-J |
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Gene:
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Spta1
Location:
Chr1:174172776-174248450 bp, + strand
Genetic Position: Chr1,
80.97 cM
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Mutation
origin |
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Single point mutation |
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Mutation details: The mutation in the sph-ha mouse (also known as sph-J) was identified as a C to A transversion in exon 52 that converts a tyrosine to a stop codon. This mutation truncates the protein by 13 amino acids. (J:81125)
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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:24729
Bernstein S,
"New mutant: Hemolytic anemia - ha"
Mouse News Lett 1960;23():33
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All: |
18 reference(s)
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Analysis Tools
