1. Panels
  2. Common Variable Immunodeficiency
  3. NFKBID
STRs in panel
Prev Next
Regions in panel
Prev Next

Common Variable Immunodeficiency

Gene: NFKBID

Red List (low evidence)
NFKBID (NFKB inhibitor delta)
EnsemblGeneIds (GRCh38): ENSG00000167604
EnsemblGeneIds (GRCh37): ENSG00000167604
NFKBID is in 4 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for Mendelian gene-disease association in humans; mouse model data only.
Created: 11 Apr 2020, 4:40 a.m. | Last Modified: 11 Apr 2020, 4:40 a.m.
Panel Version: 0.21

Publications

Created: 11 Apr 2020, 4:40 a.m.
Last Modified: 11 Apr 2020, 4:40 a.m.
Panel version: 0.21

Details

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

History Filter Activity

11 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

11 Apr 2020, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: NFKBID were set to

11 Apr 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: nfkbid 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: NFKBID was added gene: NFKBID was added to Common Variable Immunodeficiency_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: NFKBID was set to Unknown