1. Panels
  2. Monogenic Diabetes
  3. HAMP
STRs in panel
Prev Next
Regions in panel
Prev Next

Monogenic Diabetes

Gene: HAMP

Green List (high evidence)
HAMP (hepcidin antimicrobial peptide)
EnsemblGeneIds (GRCh38): ENSG00000105697
EnsemblGeneIds (GRCh37): ENSG00000105697
OMIM: 606464, Gene2Phenotype
HAMP is in 9 panels

1 review

Hali Van Niel (University of Melbourne)

Green List (high evidence)

established gene disease associated for hemochromatosis type 2B (severe inherited iron-loading disorder, juvenile presentation), typical manifestation includes diabetes.
Created: 2 May 2024, 2:48 a.m. | Last Modified: 2 May 2024, 2:48 a.m.
Panel Version: 0.58

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
hemochromatosis type 2B MONDO:0013220

Publications

Created: 2 May 2024, 2:48 a.m.
Last Modified: 2 May 2024, 2:48 a.m.
Panel version: 0.58

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Hemochromatosis, type 2B 613313
OMIM
606464
Clinvar variants
Variants in HAMP
Penetrance
None
Publications
Panels with this gene

History Filter Activity

2 May 2024, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

2 May 2024, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: HAMP were set to

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: HAMP was added gene: HAMP was added to Monogenic diabetes. Sources: Expert Review,Expert Review Green Mode of inheritance for gene: HAMP was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: HAMP were set to Hemochromatosis, type 2B 613313