ATP5J

ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6
OMIM: 603152, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber ATP5J in Mitochondrial disorder with complex V deficiency Version 2.16 Latest signed off version: v2.0 (22 Mar 2023)	review	Unknown	Sources Expert Review Amber NHS GMS Phenotypes No OMIM phenotype Tags new-gene-name
Red ATP5J in Likely inborn error of metabolism - targeted testing not possible Version 4.137 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders Unexplained death in infancy and sudden unexplained death in childhood	review	Unknown	Sources Expert Review Red Phenotypes No OMIM phenotype Tags new-gene-name
Amber ATP5J in Possible mitochondrial disorder - nuclear genes Version 3.105 Latest signed off version: v3.0 (22 Mar 2023)	review	Unknown	Sources Expert Review Amber NHS GMS Phenotypes No OMIM phenotype Tags new-gene-name
Red ATP5J in Mitochondrial disorders Level 3: Mitochondrial Level 2: Metabolic disorders Version 4.168 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Childhood onset leukodystrophy	review	Not set	Sources Expert Review Red Radboud University Medical Center, Nijmegen Phenotypes No OMIM phenotype Tags new-gene-name