HFE
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 6[11]
- Cytogenetic location
- 6p22.2[17]
- Expressed in
- stromal cell of endometrium, Epithelium of choroid plexus, monocyte, right adrenal cortex, smooth muscle tissue, cervix epithelium, seminal vesicula, left adrenal gland, Achilles tendon, gallbladder[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- cardiovascular disease, arterial hypertension, variegate porphyria, hemochromatosis type 1[12][13][14][15]
- HomoloGene ID
- 88330[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en hemochromatosis
en HFE
en HFE1
en HFE gene
en HH
en HLA-H
en homeostatic iron regulator
en MVCD7
en TFQTL2
es gen HFE
fr gène HFE
zh HFE (基因)
🔖 Identifiers · 10
- Image (Wikimedia Commons)
- Protein HFE PDB 1a6z.png ↗
- Ensembl gene ID
- ENSG00000010704
- Ensembl transcript ID
- ENST00000488199, ENST00000309234, ENST00000317896, ENST00000336625, ENST00000349999, ENST00000352392, ENST00000353147, ENST00000357618, ENST00000397022, ENST00000461397, ENST00000470149, ENST00000483782, ENST00000485729, ENST00000486147
- Entrez Gene ID
- 3077
- Exact match
- identifiers.org
- HGNC ID
- 4886
- HGNC gene symbol
- HFE
- OMIM ID
- 613609
- RefSeq RNA ID
- XR_241893, NM_000410, NM_001300749, NM_139002, NM_139003, NM_139004, NM_139005, NM_139006, NM_139007, NM_139008, NM_139009, NM_139010, NM_139011, NM_001384164
- UMLS CUI
- C1384665
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Summary
HFE is a gene[1].