Isolation and mapping of a polymorphic CA repeat sequence at the human VRK1 locus

J Hum Genet. 1999;44(2):133-4. doi: 10.1007/s100380050127.

Abstract

VRK1 is a novel human putative serine/threonine kinase, and is located on chromosome 14 at band q32 where an autosomal recessive congenital microphthalmia (CMIC) is mapped. We isolated a polymorphic dinucleotide CA repeat marker from a genomic clone containing the human VRK1 gene. This polymorphism will be useful in genetic studies of disorders localized at the 14q32 region, such as CMIC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 14
  • DNA Primers
  • Dinucleotide Repeats*
  • Eye Abnormalities / genetics
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Protein Serine-Threonine Kinases / genetics*
  • Proteins*
  • Viral Proteins / genetics*

Substances

  • DNA Primers
  • Intracellular Signaling Peptides and Proteins
  • Proteins
  • Viral Proteins
  • Protein Serine-Threonine Kinases
  • VRK1 protein, human

Associated data

  • GENBANK/AB025785