PanelApp (staging)
  1. Genes and Genomic Entities
  2. NDUFB10

NDUFB10

NADH:ubiquinone oxidoreductase subunit B10
OMIM: 603843, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green NDUFB10 in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • fatal infantile lactic acidosis
  • cardiomyopathy
  • Mitochondrial complex I deficiency nuclear type 35 (MC1DN35), MIM#619003

Green NDUFB10 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.969

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • fatal infantile lactic acidosis
    • cardiomyopathy
    • Mitochondrial complex I deficiency nuclear type 35 (MC1DN35), MIM#619003