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Mendeliome

Gene: NDUFS5

Red List (low evidence)

NDUFS5 (NADH:ubiquinone oxidoreductase subunit S5)
EnsemblGeneIds (GRCh38): ENSG00000168653
EnsemblGeneIds (GRCh37): ENSG00000168653
OMIM: 603847, Gene2Phenotype
NDUFS5 is in 1 panel

1 review

Krithika Murali (Victorian Clinical Genetics Services)

Red List (low evidence)

No Mendelian gene disease association reported.
Created: 21 Mar 2022, 5:30 a.m. | Last Modified: 21 Mar 2022, 5:30 a.m.
Panel Version: 0.11667

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
603847
Clinvar variants
Variants in NDUFS5
Penetrance
None
Panels with this gene

History Filter Activity

22 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ndufs5 has been classified as Red List (Low Evidence).

22 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ndufs5 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: NDUFS5 was added gene: NDUFS5 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: NDUFS5 was set to Unknown