PanelApp
  1. Genes and Genomic Entities
  2. ATP5F1

ATP5F1

ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1
OMIM: 603270, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ATP5F1 in Mendeliome


Version 1.3520

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation-2 (HUMOP2), MIM#620085

Red ATP5F1 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.1085

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation-2 (HUMOP2), MIM#620085