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H2-Kbm1
Spontaneous Allele Detail
Nomenclature
Symbol: H2-Kbm1
Name: histocompatibility 2, K region; b haplotype mutation 1
MGI ID: MGI:3618114
Synonyms: bm1, H-2ba, H-2bm1, H(z1), Kbm1
Gene: H2-K  Location: unknown  Genetic Position: Chr17, Syntenic
Mutation
origin
Strain of Origin:  C57BL/6By
Mutation
description
Allele Type:    Spontaneous
Mutation:    Nucleotide substitutions
 
Mutation detailsThe 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)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 10 strains available      Cell Lines: 0 lines available
Carrying any H2-K Mutation:  31 strains or lines available
Notes
Genbank ID for this allele: X56624
References
Original:  J:164063 Bailey DW, et al., Complementation and Serolgical Analysis of an H-2 Mutant, in Proc Symp Immunogenetics of the H-2 System, Liblice-Prague 1970. 1971:155-162.
All:  93 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/05/2019
MGI 6.14
The Jackson Laboratory