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Molecular autopsy

Gene: NDUFB8

Red List (low evidence)
NDUFB8 (NADH:ubiquinone oxidoreductase subunit B8)
EnsemblGeneIds (GRCh38): ENSG00000166136
EnsemblGeneIds (GRCh37): ENSG00000166136
OMIM: 602140, Gene2Phenotype
NDUFB8 is in 6 panels

0 reviews

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
Phenotypes
  • No OMIM phenotype
  • Isolated complex I deficiency
OMIM
602140
Clinvar variants
Variants in NDUFB8
Penetrance
None
Panels with this gene

History Filter Activity

20 Dec 2018, Gel status: 1

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes No OMIM phenotype; Isolated complex I deficiency for gene: NDUFB8

20 Dec 2018, Gel status: 1

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes No OMIM phenotype; Isolated complex I deficiency for gene: NDUFB8

20 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: NDUFB8 was added gene: NDUFB8 was added to Molecular autopsy. Sources: Expert Review Red Mode of inheritance for gene: NDUFB8 was set to Unknown Phenotypes for gene: NDUFB8 were set to No OMIM phenotype; Isolated complex I deficiency