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Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.

H ShinoY Otsuka-YamasakiT SatoK OoiO InanamiR SatoYayoi Otsuka
Published in: Journal of veterinary internal medicine (2018)
This dog family had familial congenital methemoglobinemia caused by b5R deficiency, which resulted from a nonsynonymous variant in the CYB5R3 gene. This variation (c.580A>C) led to an amino acid substitution (p.Ile194Leu), and Ile194 was located in the proximal region of the NADH-binding motif. Our data suggested that this variant in the canine CYB5R3 gene would affect function of the b5R in erythrocytes.
Keyphrases
  • copy number
  • genome wide
  • amino acid
  • genome wide identification
  • early onset
  • dna methylation
  • gene expression
  • intellectual disability
  • machine learning
  • dna binding
  • smoking cessation