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Allele : H2-K<bm29> histocompatibility 2, K region; b haplotype mutation 29

Primary Identifier  MGI:3618265 Allele Type  Spontaneous
Gene  H2-K Strain of Origin  (C3.CAS3(R4) x C57BL/6)F2
Is Recombinase  false Is Wild Type  false
description  Genbank ID for this allele: M34542
molecularNote  The bm29 sequence differs from the parental sequence by two nucleotide substitutions at codon 89, resulting in a lysine to alanine substitution. This mutation is thought to have arised by a gene conversion-like event.
  • mutations:
  • Nucleotide substitutions
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories

Trail: Allele