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Basic information of HAMP :

Official Symbol of Gene HAMP
Species Homo sapiens
Entrez Gene ID 57817
Official Full Name hepcidin antimicrobial peptide
Also known as HEPC; PLTR; HFE2B; LEAP1
Gene Type protein coding
dbXrefs Ensembl:ENSG00000105697 MIM:606464; AllianceGenome:HGNC:15598
Map Location 19q13.12
Variation Type SNP
refSNP ID rs10421768

Sample information of multiple sclerosis:

Detected Sample peripheral blood leukocytes
Sample Detail N/A
Detected Method Real-time PCR
Disease MS
Disease subtype RRMS, PPMS, SPMS
Population N/A
Sample Size 176 MS patients

Literature information of multiple sclerosis :

Pubmed ID 35682458
Year 2022
Title Hepcidin (rs10421768), Transferrin (rs3811647, rs1049296) and Transferrin Receptor 2 (rs7385804) Gene Polymorphism Might Be Associated with the Origin of Multiple Sclerosis

Results of multiple sclerosis :

Risk Type Phenotypic risk
Main Result Positive
Result A statistical trend has been shown regarding the tendency to occur primary relapses more frequently among persons with the AA + AG genotype compared with GG patients in the recessive HAMP rs10421768 inheritance model.
Mechanism/Pathway The mechanism of iron regulation in the cell by HAMP is mainly based on the control of FPN expression at the level of its translation.The presence of polymorphisms in the genes of iron metabolism may modulate iron deposition in the body and thus affect the clinical course of the disease.