Genome Browser


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Gene Information

Gene Symbol HFE
Gene Aliases HFE1|HH|HLA-H|MGC103790|dJ221C16.10.1
Gene Name hemochromatosis
Gene ID 3077
Cytogenetic Band 6p21.3
Gene Type protein-coding
mitoDat ID  

Disease Information

Disease Hit 34
Disease Name Hemochromatosis
Variegate Porphyria
Colorectal Cancer
Arthritis
Cirrhosis
AZALEKO TUMORE GAIZTOA
Alzheimer's Disease
Hepatitis C
Porphyria Cutanea Tarda
UGATZ TUMORE GAIZTOA
Rheumatoid Arthritis
Malignant neoplasm of liver
Hepatitis C, Chronic
Chronic Fatigue Syndrome
Diabetic Retinopathy
Jaundice, Chronic Idiopathic
Diabetes
Iron Overload
Coronary heart disease
Diabetes Mellitus, Non-Insulin-Dependent
Insulin Resistance
Hereditary hemochromatosis
Myocardial Ischemia
Parkinson Disease
Malignant tumor of colon
Cystic Fibrosis
Genetic Markers
Longevity
Life Expectancy
Cardiomyopathies
Atherosclerosis
Cardiovascular Diseases
Coronary Arteriosclerosis
Myocardial Infarction
Others no cui diseases

Transcription Information

No mRNA Accession Chromosome Position Strand Exon Count Promoter
SNP
Count		 5'UTR SNP Count CDS SNP Count 3'UTR SNP Count Intron SNP Count
1 NM_000410 chr6:26195488~
26203448		 + 1 11 0 9 2 22
2 NM_139002 chr6:26195488~
26205035		 + 1 11 0 6 1 38
3 NM_139003 chr6:26195488~
26203448		 + 1 11 0 7 2 24
4 NM_139004 chr6:26195488~
26203448		 + 1 11 0 8 2 23
5 NM_139005 chr6:26195488~
26205035		 + 1 11 0 7 3 35
6 NM_139006 chr6:26195488~
26203448		 + 1 11 0 8 2 23
7 NM_139007 chr6:26195488~
26203448		 + 1 11 0 4 2 27
8 NM_139008 chr6:26195488~
26203448		 + 1 11 0 3 2 28
9 NM_139009 chr6:26195488~
26203448		 + 1 11 0 8 2 23
10 NM_139010 chr6:26195488~
26203448		 + 1 11 0 3 2 28
11 NM_139011 chr6:26195488~
26203448		 + 1 11 0 1 2 30

SNP Information

SNP ID Chromosome Chromosome Position Strand Allele Fuction Class
rs12528294 6 26192509 + G/T Promoter
rs12526555 6 26192515 + A/G Promoter
rs1090949 6 26193375 - A/G Promoter
rs1971509 6 26193756 - A/G Promoter
rs1971508 6 26193786 - G/T Promoter
rs7741769 6 26193788 + A/G Promoter
rs2006736 6 26193996 - A/G Promoter
rs35646118 6 26194394..26194395 + -/G Promoter
rs1800702 6 26194442 + C/G Promoter
rs1061482 6 26194678 - A/C Promoter
rs2794720 6 26195181 - C/G Promoter
rs2858993 6 26195835 + A/T Intron
rs807206 6 26196268 - A/T Intron
rs3799374 6 26196386 + A/G Intron
rs2794719 6 26196869 - A/C Intron
rs9366637 6 26197077 + C/T Intron
rs807207 6 26197315 - A/C Intron
rs34555420 6 26198249 + G/T Intron
rs2858994 6 26198372 + A/T Intron
rs13196986 6 26198431 + C/T Intron
rs2227837 6 26198982 + C/T Intron
rs2242956 6 26199075 + C/T CDS-nonsynonymous, Intron
rs1799945 6 26199158 + C/G CDS-nonsynonymous, Intron
rs1800730 6 26199164 + A/T CDS-nonsynonymous, Intron
rs28934597 6 26199248 + C/G CDS-nonsynonymous, Intron
rs28934596 6 26199285 + C/T CDS-nonsynonymous, Intron
rs2071303 6 26199315 - A/G Intron
rs28934595 6 26199561 + A/C CDS-nonsynonymous, Intron
rs2227838 6 26199827 + C/T Intron
rs807208 6 26200126 - A/G Intron
rs2032451 6 26200149 - A/C Intron
rs34225963 6 26200403 + -/A Intron
rs807209 6 26200844 - C/G Intron
rs4986950 6 26200925 + C/T CDS-nonsynonymous, Intron
rs1800562 6 26201120 + A/G CDS-nonsynonymous, Intron
rs1800758 6 26201215 + A/G Intron
rs2794717 6 26201276 - C/T Intron
rs1800708 6 26201282 + C/T Intron
rs2858996 6 26202005 + G/T Intron
rs2071302 6 26202109 - A/G Intron
rs1572982 6 26202346 + A/G Intron
rs35201683 6 26202412 + C/T CDS-synonymous, Intron
rs3177318 6 26202948 + C/T 3UTR, Intron
rs1045533 6 26203007 + A/G 3UTR, Intron
rs13210399 6 26203622 + A/G Intron
rs7762959 6 26203644 + C/T Intron
rs1132675 6 26203678 + A/G Intron
rs11465177 6 26203715..26203716 + -/A Intron
rs28655685 6 26203715 + A/T Intron
rs34409072 6 26203725 + -/A Intron
rs707889 6 26203910 - C/T Intron
rs35321356 6 26203942 + -/A Intron
rs11415491 6 26204363..26204364 + -/T Intron
rs11545102 6 26204709 - A/G 3UTR, Intron
rs1045537 6 26204727 + C/G 3UTR, Intron
rs12346 6 26205025 - A/G 3UTR

Selected Disease


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