HFE
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Homo sapiens |
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HFE is differentially expressed in 340 experiments: 184 organism parts: ovary, skin, ... (182 more);, 298 disease states: normal, breast carcinoma, ... (296 more);, 115 cell types 529 cell lines 50 compound treatments and 82 other conditions. |
| Synonyms |
HLA-H |
| Orthologs |
ENSGALG00000011014
(Gallus gallus)
CABZ01031754.1
(Danio rerio)
F1NH73_CHICK
(Gallus gallus)
ENSGALG00000012967
(Gallus gallus)
F1N816_CHICK
(Gallus gallus)
ENSGALG00000004617
(Gallus gallus)
mhc1ze
(Danio rerio)
CABZ01089980.1
(Danio rerio)
ENSGALG00000000180
(Gallus gallus)
F1NS77_CHICK
(Gallus gallus)
zgc:136614
(Danio rerio)
CABZ01029904.1
(Danio rerio)
mhc1uba
(Danio rerio)
ENSGALG00000005825
(Gallus gallus)
Q5EEZ1_BOVIN
(Bos taurus)
ENSGALG00000017674
(Gallus gallus)
si:ch211-287j19.6
(Danio rerio)
zgc:64115
(Danio rerio)
CABZ01031753.1
(Danio rerio)
Hfe
(Mus musculus)
ENSGALG00000024427
(Gallus gallus)
F1NFX9_CHICK
(Gallus gallus)
F1NKF8_CHICK
(Gallus gallus)
F1NED2_CHICK
(Gallus gallus)
F1NKE5_CHICK
(Gallus gallus)
F1NM79_CHICK
(Gallus gallus)
Hfe
(Rattus norvegicus)
ENSXETG00000002125
(Xenopus laevis)
LOC100494930
(Xenopus laevis)
XB-GENE-5873924
(Xenopus laevis)
XB-GENE-5894693
(Xenopus laevis)
mhc1a
(Xenopus laevis)
LOC100490553
(Xenopus laevis)
NP_001123818.1
(Xenopus laevis)
mhc1zel
(Danio rerio)
LOC100490728
(Xenopus laevis)
ENSXETG00000030515
(Xenopus laevis)
LOC100487860
(Xenopus laevis)
si:ch73-213j4.4
(Danio rerio)
XB-GENE-5757686
(Xenopus laevis)
ENSXETG00000033980
(Xenopus laevis)
LOC100495225
(Xenopus laevis)
LOC100493954
(Xenopus laevis)
ENSXETG00000032875
(Xenopus laevis)
NP_001123671.1
(Xenopus laevis)
ENSXETG00000017938
(Xenopus laevis)
ENSXETG00000009068
(Xenopus laevis)
LOC100494293
(Xenopus laevis)
LOC100495868
(Xenopus laevis)
LOC100495703
(Xenopus laevis)
LOC100495542
(Xenopus laevis)
ENSXETG00000033834
(Xenopus laevis)
ENSXETG00000009089
(Xenopus laevis)
ENSXETG00000031111
(Xenopus laevis)
mr1
(Xenopus laevis)
HFE
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
plasma membrane, protein binding, cytoplasm, basal part of cell, ion transport, membrane, receptor-mediated endocytosis, protein complex assembly, recycling endosome, iron ion transport, early endosome, cellular response to iron ion starvation, integral to plasma membrane, immune response, cytoplasmic vesicle, perinuclear region of cytoplasm, apical part of cell, integral to membrane, cellular iron ion homeostasis, female pregnancy, iron ion homeostasis, antigen processing and presentation of peptide antigen via MHC class I, MHC class I protein complex, hormone biosynthetic process, antigen processing and presentation, multicellular organismal iron ion homeostasis |
| Gene Ontology ID |
GO:0016020, GO:0016021, GO:0010106, GO:0048471, GO:0005515, GO:0006955, GO:0005737, GO:0006879, GO:0006898, GO:0005886, GO:0005887, GO:0005769, GO:0055037, GO:0006811, GO:0006826, GO:0006461, GO:0031410, GO:0045177, GO:0045178, GO:0060586, GO:0007565, GO:0042446, GO:0002474, GO:0042612, GO:0055072, GO:0019882 |
| InterPro Term |
Ig_C1-set, Ig-like, MHC_I_a_a1/a2 |
| InterPro ID |
IPR007110, IPR003597, IPR001039 |
| Ensembl Family |
ENSFM00400000131848 |
| Ensembl Family Description |
HEREDITARY HEMOCHROMATOSIS HOMOLOG PRECURSOR |
| Description |
hemochromatosis [Source:HGNC Symbol;Acc:4886] |
| UniProt Accession |
Q96KU6, Q9UK37, Q6B0J5, Q86WL1, Q9HC69, Q30201, Q8MH46, Q9BXI5, F5B2M9, F5H4B0, F8W7W8 |
| EMBL-Bank ID |
AF115265, AF115264, AF079407, AF079408, AF079409, U91328, AF149804, BC074721, AF525499, AF525359, AY205604, U60319, EU523119, Y09800, Y09801, Y09803, CH471087, AJ249338, AJ249335, AJ249337, AJ249336, AF331065, Y09799, AF144241, AF144242, AF144240, BC117201, BC117203, AJ250635, Z92910, AF184234, HQ602968 |
| Ensembl Protein ID |
ENSP00000315936, ENSP00000311698, ENSP00000337819, ENSP00000259699, ENSP00000313776, ENSP00000312342, ENSP00000419725, ENSP00000417534, ENSP00000417404, ENSP00000420559, ENSP00000420802, ENSP00000380217, ENSP00000445872, ENSP00000445098 |
| Gene-Disease Assocation |
PORPHYRIA CUTANEA TARDA, PORPHYRIA VARIEGATA, MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7; MVCD7, HEMOCHROMATOSIS; HFE, ALZHEIMER DISEASE; AD, TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2; TFQTL2 |
| Ensembl Gene ID |
ENSG00000010704 |
| RefSeq ID |
NP_620577, NP_620576, NP_620579, NP_620578, NP_620573, NP_620572, NP_620575, NP_620580, NP_000401, NM_000410, NM_139008, NM_139009, NM_139011, NM_139010, NM_139003, NM_139006, NM_139007, NM_139004 |
| UniGene ID |
Hs.233325 |
| Entrez Gene ID |
3077 |
| HGNC Symbol |
HFE |
| Ensembl Transcript ID |
ENST00000485729, ENST00000309234, ENST00000336625, ENST00000349999, ENST00000352392, ENST00000539147, ENST00000488199, ENST00000317896, ENST00000486147, ENST00000483782, ENST00000397022, ENST00000470149, ENST00000535098, ENST00000353147, ENST00000461397, ENST00000357618 |
| Design Element |
ENST00000483782, 211326_3p_x_at, 211863_x_at, 211330_s_at, g11094328_3p_x_at, 214647_s_at, 1553402_a_at, 211326_x_at, g11093525_3p_at, ENST00000349999, ENST00000353147, 38913_at, 211329_x_at, 235754_at, ENST00000357618, 211327_x_at, ENST00000539147, ENST00000486147, g11094326_3p_a_at, ENST00000309234, ENST00000317896, g11094324_3p_a_at, 210864_x_at, U60319_at, ENST00000470149, 206087_x_at, g3695110_3p_a_at, g4504376_3p_x_at, Hs.20019.12.S2_3p_a_at, g11094322_3p_x_at, g11094326_3p_x_at, g11093523_3p_x_at, 211866_x_at, Hs.107216.0.A1_3p_at, 80609_at, ENST00000535098, 50508_at, 211328_x_at, ENST00000397022, g11094320_3p_x_at, 211332_x_at, ENST00000336625, 211331_x_at, g11094314_3p_a_at, g3695108_3p_a_at, 211866_3p_x_at, 211863_3p_x_at, 50664_at, g11093525_3p_x_at, ENST00000488199, 206086_3p_x_at, 206086_x_at, ENST00000352392, g11093525_3p_a_at, ENST00000485729, g11094320_3p_a_at, ENST00000461397, g11093523_3p_s_at |
| Search EB-eye |
ENSG00000010704
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