A novel KIR2DL3 variant allele, KIR2DL3*032, which has arisen by a missense mutation in codon 231

Tissue Antigens. 2015 Feb;85(2):150-1. doi: 10.1111/tan.12499.

Abstract

The novel 2DL3*032 allele differs from the closest allele KIR2DL3*0010101 by a non-synonymous mutation in exon 7.

Keywords: 2DL3*032; novel allele; sequence-based typing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Base Sequence
  • Codon / genetics*
  • Humans
  • Molecular Sequence Data
  • Mutation, Missense / genetics*
  • Receptors, KIR2DL3 / genetics*
  • Sequence Alignment

Substances

  • Codon
  • KIR2DL3 protein, human
  • Receptors, KIR2DL3

Associated data

  • GENBANK/KF849248