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

Symbol:	H2-D1bm13
Name:	histocompatibility 2, D region locus 1; b haplotype mutation 13
MGI ID:	MGI:3618116
Synonyms:	H-2bn
Gene:	H2-D1  Location: Chr17:35482070-35486473 bp, + strand  Genetic Position: Chr17, 18.61 cM
Alliance:	H2-D1bm13 page

Strain of Origin:

(C57BL/6ByKh x BALB/cByKh)F1

Allele Type:    Spontaneous Mutation:    Nucleotide substitutions   Mutation details: The bm13 mutation consists of four nucleotide changes that result in amino acid changes in codons 114 (leucine to glycine), 116 (phenylalanine to tyrosine) and 119 (glutamate to aspartate). A mutation in codon 118 is silent. The mutation is thought to have arisen by a gene conversion event with the H-2Kb acting as the donor locus. (J:106337)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any H2-D1 Mutation:	45 strains or lines available

Original:	J:106349 Melvold RW, et al., Eight new histocompatibility mutations associated with the H-2 complex. Immunogenetics. 1976;3:185-191
All:	16 reference(s)