1. Panels
  2. Monogenic Diabetes
  3. HFE2
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Monogenic Diabetes

Gene: HFE2

Green List (high evidence)
HFE2 (hemochromatosis type 2 (juvenile))
EnsemblGeneIds (GRCh38): ENSG00000168509
EnsemblGeneIds (GRCh37): ENSG00000168509
OMIM: 608374, Gene2Phenotype
HFE2 is in 9 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Comment when marking as ready: HGNC approved name is HJV.
Created: 9 Aug 2020, 2:59 a.m. | Last Modified: 9 Aug 2020, 2:59 a.m.
Panel Version: 0.4
Created: 9 Aug 2020, 2:59 a.m.
Last Modified: 9 Aug 2020, 2:59 a.m.
Panel version: 0.4

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Hemochromatosis, type 2A, 602390
Tags
new gene name
OMIM
608374
Clinvar variants
Variants in HFE2
Penetrance
None
Panels with this gene

History Filter Activity

9 Aug 2020, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: hfe2 has been classified as Green List (High Evidence).

9 Aug 2020, Gel status: 3

Added Tag

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Tag new gene name tag was added to gene: HFE2.

17 Jan 2020, Gel status: 3

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: HFE2 was added gene: HFE2 was added to Monogenic diabetes. Sources: Expert Review,Expert Review Green Mode of inheritance for gene: HFE2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: HFE2 were set to Hemochromatosis, type 2A, 602390