Isolation and chromosomal mapping of a mouse homolog of the Batten disease gene CLN3

Genomics. 1996 Aug 1;35(3):617-9. doi: 10.1006/geno.1996.0410.

Abstract

We describe the isolation and chromosomal mapping of a mouse homolog of the Batten disease gene, CLN3. Like its human counterpart, the mouse cDNA contains an open reading frame of 1314 bp encoding a predicted protein product of 438 amino acids. The mouse and human coding regions are 82 and 85% identical at the nucleic acid and amino acid levels, respectively. The mouse gene maps to distal Chromosome 7, in a region containing genes whose homologs are on human chromosome 16p12, where CLN3 maps. Isolation of a mouse CLN3 homolog will facilitate the creation of a mouse model of Batten disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Chromosome Mapping*
  • DNA, Complementary
  • Female
  • Humans
  • Male
  • Membrane Glycoproteins*
  • Mice
  • Mice, Inbred C57BL
  • Molecular Chaperones*
  • Molecular Sequence Data
  • Neuronal Ceroid-Lipofuscinoses / genetics*
  • Proteins / genetics*

Substances

  • CLN3 protein, mouse
  • DNA, Complementary
  • Membrane Glycoproteins
  • Molecular Chaperones
  • Proteins

Associated data

  • GENBANK/U32680
  • GENBANK/U47106