|  Help  |  About  |  Contact Us

Allele : H2-K<bm1> histocompatibility 2, K region; b haplotype mutation 1

Primary Identifier  MGI:3618114 Allele Type  Spontaneous
Gene  H2-K Strain of Origin  C57BL/6By
Is Recombinase  false Is Wild Type  false
description  Genbank ID for this allele: X56624
molecularNote  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).
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • H-2<ba>,
  • H-2<ba>,
  • H(z1),
  • K<bm1>,
  • bm1,
  • bm1,
  • K<bm1>,
  • H-2<bm1>,
  • H-2<bm1>,
  • H(z1)
Quick Links:
 
Quick Links:
 

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

9 Carried By

0 Driven By

100 Publication categories