ATP7B
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Homo sapiens |
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ATP7B is differentially expressed in 241 experiments: 94 organism parts: liver, cerebellum, ... (92 more);, 140 disease states: normal, glioblastoma, ... (138 more);, 58 cell types 324 cell lines 30 compound treatments and 75 other conditions. |
| Synonyms |
WND |
| Orthologs |
Atp7b
(Rattus norvegicus)
F1MKI1_BOVIN
(Bos taurus)
ATP7B
(Danio rerio)
F1N8W2_CHICK
(Gallus gallus)
Atp7b
(Mus musculus)
ATP7
(Drosophila melanogaster)
CCC2
(Saccharomyces cerevisiae)
F6SW46_CIOIN
(Ciona intestinalis)
atp7b
(Xenopus laevis)
NP_001020438.1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008152, GO:0016020, GO:0016021, GO:0016023, GO:0003824, GO:0016323, GO:0051208, GO:0004008, GO:0016787, GO:0048471, GO:0005622, GO:0005624, GO:0005524, GO:0005507, GO:0005515, GO:0015677, GO:0015662, GO:0005737, GO:0005739, GO:0006878, GO:0005802, GO:0005887, GO:0005794, GO:0005770, GO:0006754, GO:0055085, GO:0006812, GO:0006825, GO:0000166, GO:0000139, GO:0046872, GO:0046688, GO:0030001, GO:0060003, GO:0007595, GO:0015680, GO:0043682, GO:0006882, GO:0006200, GO:0034220 |
| Gene Ontology Term |
ATPase activity, coupled to transmembrane movement of ions, phosphorylative mechanism, response to copper ion, protein binding, cytoplasm, copper-exporting ATPase activity, intracellular, metal ion transport, membrane, cellular copper ion homeostasis, Golgi membrane, Golgi apparatus, metabolic process, metal ion binding, cation transport, late endosome, membrane fraction, basolateral plasma membrane, ATP binding, sequestering of calcium ion, integral to plasma membrane, copper ion import, copper ion transport, cytoplasmic membrane-bounded vesicle, nucleotide binding, ATP biosynthetic process, perinuclear region of cytoplasm, integral to membrane, hydrolase activity, trans-Golgi network, transmembrane transport, catalytic activity, copper ion binding, mitochondrion, cellular zinc ion homeostasis, copper-transporting ATPase activity, lactation, ATP catabolic process, copper ion export, intracellular copper ion transport, ion transmembrane transport |
| InterPro Term |
Dehalogen-like_hydro, ATPase_P-typ_heavy-metal, ATPase_P-typ_H-transp, HAD-SF_hydro-like_3, ATPase_P-typ_ion-transptr, ATPase_P-typ_cat/Cu-transptr, ATPase_P-typ_ATPase-assoc-dom, HG_scavenger, HMA_Cu_ion-bd, HeavyMe-assoc_HMA |
| InterPro ID |
IPR005834, IPR001757, IPR006416, IPR006403, IPR000695, IPR008250, IPR006122, IPR006121, IPR013200, IPR001802 |
| Ensembl Family |
ENSFM00570000851002 |
| Ensembl Family Description |
COPPER TRANSPORTING ATPASE EC_3.6.3.4 COPPER PUMP DISEASE ASSOCIATED |
| EMBL-Bank ID |
GU471212, GU471213, GQ250097, DQ015922, U03464, EF643604, EF643606, EU047913, EF620914, L25442, FJ705811, L25591, AB209461, AF034838, AL139082, EU041762, S77450, S77446, S77447, AL162377, AL138821, U11700 |
| Gene-Disease Assocation |
WILSON DISEASE |
| RefSeq ID |
NM_001005918, NP_001005918, NP_000044, NM_000053, NM_001243182, NP_001230111 |
| Ensembl Protein ID |
ENSP00000342559, ENSP00000383221, ENSP00000383217, ENSP00000416738, ENSP00000242839, ENSP00000390360, ENSP00000393343, ENSP00000443128 |
| UniProt Accession |
D3KCZ0, A6N865, C0LF55, A7UAV8, P35670, A7UDR4, A6YQZ0, A6YQZ1, C8BMD5, E7EQQ2, E7ET55, F6XIH0, F5H748, F5H562 |
| UniGene ID |
Hs.492280 |
| HGNC Symbol |
ATP7B |
| Ensembl Gene ID |
ENSG00000123191 |
| Description |
ATPase, Cu++ transporting, beta polypeptide [Source:HGNC Symbol;Acc:870] |
| Entrez Gene ID |
540 |
| Ensembl Transcript ID |
ENST00000242839, ENST00000417240, ENST00000482841, ENST00000542656, ENST00000400366, ENST00000400370, ENST00000483772, ENST00000418097, ENST00000466629, ENST00000448424, ENST00000344297 |
| Design Element |
204624_at, ENST00000344297, g4502322_3p_at, ENST00000400370, ENST00000417240, 37930_at, ENST00000482841, ENST00000542656, ENST00000448424, ENST00000418097, ENST00000242839, ENST00000483772, ENST00000400366, ENST00000466629 |
| Search EB-eye |
ENSG00000123191
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