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| Nomenclature |
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Symbol:
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H2-Kbm1
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Name:
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histocompatibility 2, K region;
b haplotype mutation 1
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MGI ID: |
MGI:3618114 |
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Synonyms: |
bm1, H-2ba, H-2bm1, H(z1), Kbm1 |
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Gene:
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H2-K
Location:
unknown
Genetic Position: Chr17,
Syntenic
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Mutation
origin |
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Strain of Origin:
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BALB/cBy
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Nucleotide substitutions |
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Mutation details: The bm1 mutation contains 7 nucleotide differences resulting in amino acid substitutions at codon 152 (glutamate to alanine), codon 155 (arginine to tyrosine) and codon 156 (leucine to tyrosine). (J:35731, J:109263, J:109268, J:109270, J:164061)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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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 |
Genbank ID for this allele: X56624
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| References |
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Original: |
J:164063
Bailey DW et al.,
"Complementation and Serolgical Analysis of an H-2 Mutant"
1971;():155-162
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All: |
67 reference(s)
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Analysis Tools
