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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(z1), H-2ba, H-2bm1, Kbm1 |
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Gene:
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H2-K
Location:
unknown
Genetic Position: Chr17,
18.65 cM
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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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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:109263, J:109268, J:109270) |
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms
(show or
hide all annotated terms)
Genotypes are listed in the next section.
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Key:
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| hm |
homozygous |
ht |
heterozygous |
| cn |
conditional genotype |
cx |
complex: > 1 genome feature |
| tg |
involves transgenes |
ot |
other: hemizygous, indeterminate,... |
| N |
normal phenotype |
 |
expected model not found |
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Phenotypic
data by
genotype
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Phenotypic Data by Genotype
(show or
hide all phenotypic details)
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Notes |
Genbank ID for this allele: X56624
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| References |
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