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| Nomenclature |
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Symbol:
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Spta1ihj
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Name:
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spectrin alpha, erythrocytic 1;
Iasi hereditary jaundice
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MGI ID: |
MGI:3615021 |
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Synonyms: |
SphIhj |
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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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Strain of Origin:
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(HRS/J x LAH)F1
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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: This spontaneous mutation has a cytosine to thymine transition in exon 38 that changes a glutamine in repeat 18 to a stop codon (Q1853Stop). (J:157766)
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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:105409
Cirlan M et al.,
"A new type of mouse hemolytic anemia named "Iasi hereditary jaundice""
Eumorphia 3rd Annual Meeting. Barcelona, Spain 2006;(Abstracts))():105-106
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All: |
2 reference(s)
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Analysis Tools
