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| Nomenclature |
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Symbol:
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Slc4a1wan
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Name:
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solute carrier family 4 (anion exchanger), member 1;
wan
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MGI ID: |
MGI:1857347 |
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Synonyms: |
wan |
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Gene:
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Slc4a1
Location:
Chr11:102348824-102366203 bp, - strand
Genetic Position: Chr11,
66.29 cM, cytoband D
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Mutation
origin |
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Strain of Origin:
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C3H/HeJ
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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 wan mutation was shown to be a C-to-T transition in nucleotide 3998 that results in a premature stop codon at amino acid 45. (J:85321)
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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:85321
Peters LL,
"Failure of effective reticulocytosis in a new spontaneous band 3 deficient mouse strain (C3H/HeJ-wan) and in a subset of targeted band 3 null mice (B6,129 AE1-/-) suggests the presence of genetic modifiers of band 3 function in red blood cells."
Blood 1998;92(Suppl 1):301
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All: |
3 reference(s)
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Analysis Tools
