Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | Notes | References

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

Strain of Origin:

C57BL/6By

Allele Type:    Spontaneous Mutation:    Nucleotide substitutions   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)

View phenotypes and curated references for all genotypes (concatenated display).

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

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:	99 reference(s)