H2-K^bm1
Spontaneous Allele Detail

Summary

• Symbol: H2-K^bm1
• Name: histocompatibility 2, K region; b haplotype mutation 1
• MGI ID: MGI:3618114
• Synonyms: bm1, H-2^ba, H-2^bm1, H(z1), K^bm1
• 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 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)

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: 99 reference(s)