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  3. C8G
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Complement Deficiencies

Gene: C8G

Red List (low evidence)
C8G (complement C8 gamma chain)
EnsemblGeneIds (GRCh38): ENSG00000176919
EnsemblGeneIds (GRCh37): ENSG00000176919
OMIM: 120930, Gene2Phenotype
C8G is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for Mendelian gene-disease association.
Created: 10 Apr 2020, 2:02 a.m. | Last Modified: 10 Apr 2020, 2:02 a.m.
Panel Version: 0.7
Created: 10 Apr 2020, 2:02 a.m.
Last Modified: 10 Apr 2020, 2:02 a.m.
Panel version: 0.7

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Victorian Clinical Genetics Services
OMIM
120930
Clinvar variants
Variants in C8G
Penetrance
None
Panels with this gene

History Filter Activity

10 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: c8g has been classified as Red List (Low Evidence).

10 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: c8g 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: C8G was added gene: C8G was added to Complement deficiencies_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: C8G was set to Unknown