Atp7b (ATPase copper transporting beta) - Rat Genome Database

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Gene: Atp7b (ATPase copper transporting beta) Chinchilla lanigera
Analyze
Symbol: Atp7b
Name: ATPase copper transporting beta
RGD ID: 8922156
Description: ENCODES a protein that exhibits ATP binding (ortholog); copper ion binding (ortholog); copper ion transmembrane transporter activity (ortholog); INVOLVED IN cellular response to copper ion (ortholog); cellular response to manganese ion (ortholog); circadian rhythm (ortholog); PARTICIPATES IN cisplatin drug pathway; ASSOCIATED WITH Acute Liver Failure (ortholog); Anhaptoglobinemia (ortholog); Animal Disease Models (ortholog); FOUND IN apical part of cell (ortholog); basolateral plasma membrane (ortholog); bicellular tight junction (ortholog)
Type: protein-coding
RefSeq Status: MODEL
Previously known as: ATPase, Cu++ transporting, beta polypeptide; copper-transporting ATPase 2
RGD Orthologs
Human
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: ChiLan1.0 - Chinchilla ChiLan1.0 Assembly
Position:
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554315,229,126 - 5,269,616 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554315,228,395 - 5,297,120 (-)NCBIChiLan1.0ChiLan1.0
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
1 to 18 of 18 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillaAnhaptoglobinemia  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: AnhaptoglobinemiaClinVarPMID:25741868
Atp7bChinchillachromosome 13q14 deletion syndrome  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Chromosome 13q14 deletion syndromeClinVar 
Atp7bChinchillacongenital disorder of glycosylation  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Congenital disorder of glycosylationClinVarPMID:25741868 and PMID:28492532
Atp7bChinchillacongenital disorder of glycosylation Ip  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: ALG11-congenital disorder of glycosylationClinVarPMID:10441329 more ...
Atp7bChinchillaessential tremor 1  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Hand tremorClinVarPMID:25741868
Atp7bChinchillageneralized epilepsy  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Epileptic encephalopathyClinVarPMID:10790207 more ...
Atp7bChinchillagenetic disease  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:32284880 more ...
Atp7bChinchillagenetic disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:1000228 more ...
Atp7bChinchillagenetic disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:32685348 more ...
Atp7bChinchillagenetic disease  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:1000228 more ...
Atp7bChinchillahereditary breast ovarian cancer syndrome  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Breast-ovarian cancer more ...ClinVarPMID:17264425 more ...
Atp7bChinchillaintellectual disability  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
Atp7bChinchillaMental Retardation Wolff Type  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Wolff Zimmermann syndromeClinVarPMID:10441329 more ...
Atp7bChinchillaspastic ataxia  ISOATP7B (Homo sapiens)8554872ClinVar Annotator: match by term: Spastic ataxiaClinVarPMID:10441329 more ...
Atp7bChinchillaWilson disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:26207595 more ...
Atp7bChinchillaWilson disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:893844 more ...
Atp7bChinchillaWilson disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:25333069 more ...
Atp7bChinchillaWilson disease  ISOATP7B (Homo sapiens)8554872ClinVar more ...ClinVarPMID:1000228 more ...
1 to 18 of 18 rows
1 to 20 of 21 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillaAcute Liver Failure  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:25134866
Atp7bChinchillaAnimal Disease Models  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:11803042 more ...
Atp7bChinchillaBreast Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:11802810
Atp7bChinchillacarcinoma  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:11802810 and PMID:12216079
Atp7bChinchillaColorectal Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:19296535
Atp7bChinchillaDisease Progression  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:12216079 more ...
Atp7bChinchillaDyslipidemias  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:17303181
Atp7bChinchillaExperimental Liver Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:23792645
Atp7bChinchillahead and neck squamous cell carcinoma  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:12509969
Atp7bChinchillahepatitis  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:14574444 and PMID:15135151
Atp7bChinchillaInflammation  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:22945834
Atp7bChinchillaKidney Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:11509115
Atp7bChinchillaliver cirrhosis  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:25134866
Atp7bChinchillaliver disease  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:21364284
Atp7bChinchillaLiver Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:11509115
Atp7bChinchillaMouth Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:12509969
Atp7bChinchillaOvarian Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:12216079
Atp7bChinchillaProstatic Neoplasms  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:25320179
Atp7bChinchillasteatotic liver disease  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:17303181
Atp7bChinchillatesticular disease  ISOATP7B (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:38761876
1 to 20 of 21 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillaWilson disease  ISOATP7B (Homo sapiens)7240710 OMIM 


Biological Process
1 to 20 of 24 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillacellular response to copper ion  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:24614235 and REF_RGD_ID:11341682
Atp7bChinchillacellular response to manganese ion  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:24614235 and REF_RGD_ID:11341682
Atp7bChinchillacircadian rhythm  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:9920665 and REF_RGD_ID:1599396
Atp7bChinchillacopper ion export  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:24614235 and REF_RGD_ID:11341682
Atp7bChinchillacopper ion import involved_inISOATP7B (Homo sapiens)9068941 PMID:16472602UniProtPMID:16472602
Atp7bChinchillacopper ion transport involved_inISOATP7B (Homo sapiens)9068941 PMID:9837819UniProtPMID:9837819
Atp7bChinchillacopper ion transport acts_upstream_of_or_withinISOAtp7b (Mus musculus)9068941 PMID:11237756 and PMID:15634671MGIPMID:11237756 and PMID:15634671
Atp7bChinchillacopper ion transport acts_upstream_of_or_withinISOMGI:18562209068941 PMID:11085952 and PMID:11237756MGIPMID:11085952 and PMID:11237756
Atp7bChinchillacopper ion transport involved_inISOATP7B (Homo sapiens)9068941 PMID:26004889UniProtPMID:26004889
Atp7bChinchillacopper ion transport involved_inISOUniProtKB:P389959068941 PMID:12572677 and PMID:26004889UniProtPMID:12572677 and PMID:26004889
Atp7bChinchillaestablishment of localization in cell acts_upstream_of_or_withinISOMGI:18562209068941 PMID:11085952MGIPMID:11085952
Atp7bChinchillaintracellular copper ion homeostasis acts_upstream_of_or_withinISOMGI:18562209068941 PMID:11085952 more ...MGIPMID:11085952 more ...
Atp7bChinchillaintracellular copper ion homeostasis acts_upstream_of_or_withinISOMGI:21582539068941 PMID:10441329MGIPMID:10441329
Atp7bChinchillaintracellular zinc ion homeostasis acts_upstream_of_or_withinISOMGI:18562209068941 PMID:8040371 more ...MGIPMID:8040371 more ...
Atp7bChinchillalactation  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:16741141 more ...
Atp7bChinchillalactation acts_upstream_of_or_withinISOMGI:18562209068941 PMID:1588441 and PMID:6863890MGIPMID:1588441 and PMID:6863890
Atp7bChinchillalactation acts_upstream_of_or_withinISOMGI:18562219068941 MGIMGI:71982
Atp7bChinchillaprotein maturation acts_upstream_of_or_withinISOMGI:21582539068941 PMID:16436657MGIPMID:16436657
Atp7bChinchillaresponse to cAMP  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:9920665 and REF_RGD_ID:1599396
Atp7bChinchillaresponse to copper ion involved_inISOATP7B (Homo sapiens)9068941 PMID:15269005 more ...UniProtPMID:15269005 more ...
1 to 20 of 24 rows

Cellular Component
1 to 17 of 17 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillaapical part of cell  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:15994426 and REF_RGD_ID:1581816
Atp7bChinchillabasolateral plasma membrane  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:24614235 and REF_RGD_ID:11341682
Atp7bChinchillabasolateral plasma membrane located_inISOATP7B (Homo sapiens)9068941 PMID:15269005UniProtPMID:15269005
Atp7bChinchillabicellular tight junction  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:18395099 and REF_RGD_ID:2292671
Atp7bChinchillacytoplasmic vesicle located_inISOATP7B (Homo sapiens)9068941 PMID:16472602UniProtPMID:16472602
Atp7bChinchillaGolgi apparatus located_inISOATP7B (Homo sapiens)9068941 HPAGO_REF:0000052
Atp7bChinchillalate endosome located_inISOATP7B (Homo sapiens)9068941 PMID:15681833UniProtPMID:15681833
Atp7bChinchillalate endosome  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:16741141 and REF_RGD_ID:1599391
Atp7bChinchillamembrane located_inISOAtp7b (Mus musculus)9068941 PMID:10441329 and PMID:15634671MGIPMID:10441329 and PMID:15634671
Atp7bChinchillamitochondrion located_inISOATP7B (Homo sapiens)9068941 PMID:34800366FlyBasePMID:34800366
Atp7bChinchillaperinuclear region of cytoplasm  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:24614235 and REF_RGD_ID:11341682
Atp7bChinchillaperinuclear region of cytoplasm located_inISOATP7B (Homo sapiens)9068941 PMID:16939419UniProtPMID:16939419
Atp7bChinchillatight junction  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:18395099 and REF_RGD_ID:2292671
Atp7bChinchillatrans-Golgi network  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:15994426 and REF_RGD_ID:1581816
Atp7bChinchillatrans-Golgi network located_inISOAtp7b (Mus musculus)9068941 PMID:11085952MGIPMID:11085952
Atp7bChinchillatrans-Golgi network located_inISOATP7B (Homo sapiens)9068941 PMID:15269005 and PMID:16472602UniProtPMID:15269005 and PMID:16472602
Atp7bChinchillatrans-Golgi network membrane located_inISOATP7B (Homo sapiens)9068941 PMID:9837819UniProtPMID:9837819
1 to 17 of 17 rows

Molecular Function
1 to 15 of 15 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillaATP binding enablesISOATP7B (Homo sapiens)9068941 PMID:15205462 and PMID:16567646UniProtPMID:15205462 and PMID:16567646
Atp7bChinchillacopper ion binding enablesISOATP7B (Homo sapiens)9068941 PMID:12029094 and PMID:14709553HGNC-UCLPMID:12029094 and PMID:14709553
Atp7bChinchillacopper ion binding  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:14732483 and REF_RGD_ID:1581812
Atp7bChinchillacopper ion transmembrane transporter activity  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:9920665 and REF_RGD_ID:1599396
Atp7bChinchillacopper ion transmembrane transporter activity enablesISOATP7B (Homo sapiens)9068941 PMID:26004889UniProtPMID:26004889
Atp7bChinchillaP-type divalent copper transporter activity enablesISOATP7B (Homo sapiens)9068941 PMID:9837819UniProtPMID:9837819
Atp7bChinchillaP-type divalent copper transporter activity enablesISOAtp7b (Mus musculus)9068941 PMID:11237756 and PMID:15634671MGIPMID:11237756 and PMID:15634671
Atp7bChinchillaP-type divalent copper transporter activity enablesISOMGI:18562209068941 PMID:11237756MGIPMID:11237756
Atp7bChinchillaP-type divalent copper transporter activity enablesISOMGI:21582539068941 PMID:16436657MGIPMID:16436657
Atp7bChinchillaprotein binding enablesISOUniProtKB:P357549068941 PMID:16884690UniProtPMID:16884690
Atp7bChinchillaprotein binding enablesISOUniProtKB:Q8N6689068941 PMID:17919502IntActPMID:17919502
Atp7bChinchillaprotein binding enablesISOUniProtKB:O00244 and UniProtKB:Q8N6689068941 PMID:12968035IntActPMID:12968035
Atp7bChinchillaprotein binding enablesISOUniProtKB:Q9UJW09068941 PMID:16554302UniProtPMID:16554302
Atp7bChinchillaprotein binding enablesISOUniProtKB:Q055169068941 PMID:16676348UniProtPMID:16676348
Atp7bChinchillazinc ion binding  ISOAtp7b (Rattus norvegicus)9068941 RGDPMID:14732483 and REF_RGD_ID:1581812
1 to 15 of 15 rows

RGD Manual Annotations


  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Atp7bChinchillacisplatin drug pathway   ISOATP7B (Homo sapiens)9068941 RGDPMID:22796517 and REF_RGD_ID:8548473

#
Reference Title
Reference Citation
1. Transitive Annotation Pipeline Automated assignment of GO, PW and RDO ISO annotations across species
2. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
PMID:22301074  



Atp7b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554315,229,126 - 5,269,616 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554315,228,395 - 5,297,120 (-)NCBIChiLan1.0ChiLan1.0
ATP7B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381351,932,669 - 52,012,132 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1351,930,436 - 52,012,125 (-)EnsemblGRCh38hg38GRCh38
GRCh371352,506,805 - 52,586,268 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361351,404,806 - 51,483,631 (-)NCBINCBI36Build 36hg18NCBI36
Build 341351,404,805 - 51,483,631NCBI
Celera1333,555,444 - 33,634,269 (-)NCBICelera
Cytogenetic Map13q14.3NCBI
HuRef1333,295,317 - 33,374,147 (-)NCBIHuRef
CHM1_11352,473,433 - 52,553,190 (-)NCBICHM1_1
T2T-CHM13v2.01351,147,339 - 51,226,948 (-)NCBIT2T-CHM13v2.0
Atp7b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39822,482,799 - 22,550,347 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl822,482,801 - 22,550,321 (-)EnsemblGRCm39 Ensembl
GRCm38821,992,783 - 22,060,074 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl821,992,785 - 22,060,305 (-)EnsemblGRCm38mm10GRCm38
MGSCv37823,104,820 - 23,170,546 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36823,459,893 - 23,525,619 (-)NCBIMGSCv36mm8
Celera823,490,671 - 23,556,555 (-)NCBICelera
Cytogenetic Map8A2NCBI
cM Map810.78NCBI
Atp7b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81676,654,725 - 76,726,092 (+)NCBIGRCr8
mRatBN7.21669,952,286 - 70,024,404 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1669,951,778 - 70,023,636 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1675,225,956 - 75,297,317 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01678,664,533 - 78,736,202 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01673,913,825 - 73,985,530 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01674,865,516 - 74,944,935 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1674,865,516 - 74,945,286 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01674,495,179 - 74,575,822 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41674,607,988 - 74,680,080 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11674,608,239 - 74,679,614 (+)NCBI
Celera1667,837,288 - 67,908,140 (+)NCBICelera
RH 3.4 Map16664.21RGD
Cytogenetic Map16q12.5NCBI
ATP7B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21453,366,970 - 53,447,808 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11352,012,774 - 52,091,309 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01333,063,698 - 33,144,528 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11351,808,491 - 51,888,488 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1351,810,555 - 51,851,839 (-)Ensemblpanpan1.1panPan2
ATP7B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.122162,474 - 225,599 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl22191,888 - 225,266 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha22227,530 - 260,908 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.022144,381 - 208,578 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl22163,718 - 208,552 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12295,838 - 129,431 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.022145,387 - 179,042 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.022163,429 - 197,022 (+)NCBIUU_Cfam_GSD_1.0
Atp7b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945161,210,231 - 161,278,988 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365654,694,281 - 4,763,773 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365654,694,294 - 4,763,661 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ATP7B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1115,876,612 - 15,942,064 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11115,892,549 - 15,942,070 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21116,218,277 - 16,263,614 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ATP7B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1329,817,712 - 29,899,302 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl329,816,860 - 29,899,077 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605713,915,907 - 13,997,411 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Atp7b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247482,113,094 - 2,205,856 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247482,112,574 - 2,183,994 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Ensembl Acc Id: ENSCLAT00000007000   ⟹   ENSCLAP00000006888
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0 EnsemblNW_0049554315,229,126 - 5,269,616 (-)Ensembl
RefSeq Acc Id: XM_005387611   ⟹   XP_005387668
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0NW_0049554315,228,395 - 5,277,923 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005387612   ⟹   XP_005387669
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0NW_0049554315,229,126 - 5,297,120 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005387614   ⟹   XP_005387671
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0NW_0049554315,229,126 - 5,271,523 (-)NCBI
Sequence:
Protein RefSeqs XP_005387668 (Get FASTA)   NCBI Sequence Viewer  
  XP_005387669 (Get FASTA)   NCBI Sequence Viewer  
  XP_005387671 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSCLAP00000006888
  ENSCLAP00000006888.1
RefSeq Acc Id: XP_005387669   ⟸   XM_005387612
- Peptide Label: isoform X2
- UniProtKB: A0A8C2YL85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005387668   ⟸   XM_005387611
- Peptide Label: isoform X1
- UniProtKB: A0A8C2YL85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005387671   ⟸   XM_005387614
- Peptide Label: isoform X2
- UniProtKB: A0A8C2YL85 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSCLAP00000006888   ⟸   ENSCLAT00000007000
HMA



1 to 36 of 36 rows
Database
Acc Id
Source(s)
Ensembl Genes ENSCLAG00000004851 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENSCLAT00000007000 ENTREZGENE
  ENSCLAT00000007000.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.70.100 UniProtKB/TrEMBL
  3.40.1110.10 UniProtKB/TrEMBL
  3.40.50.1000 UniProtKB/TrEMBL
  Calcium-transporting ATPase, cytoplasmic transduction domain A UniProtKB/TrEMBL
InterPro ATPase_P-typ_cyto_dom_N UniProtKB/TrEMBL
  ATPase_P-typ_P_site UniProtKB/TrEMBL
  ATPase_P-typ_TM_dom_sf UniProtKB/TrEMBL
  ATPase_P-typ_transduc_dom_A_sf UniProtKB/TrEMBL
  HAD-like_sf UniProtKB/TrEMBL
  HAD_sf UniProtKB/TrEMBL
  Heavy-metal-associated_CS UniProtKB/TrEMBL
  HMA_Cu_ion-bd UniProtKB/TrEMBL
  HMA_dom UniProtKB/TrEMBL
  HMA_dom_sf UniProtKB/TrEMBL
  P-typ_ATPase_IB UniProtKB/TrEMBL
  P_typ_ATPase UniProtKB/TrEMBL
  P_typ_ATPase_HD_dom UniProtKB/TrEMBL
NCBI Gene Atp7b ENTREZGENE
PANTHER P-TYPE CATION-TRANSPORTING ATPASE UniProtKB/TrEMBL
  P-TYPE CU(+) TRANSPORTER UniProtKB/TrEMBL
Pfam E1-E2_ATPase UniProtKB/TrEMBL
  HMA UniProtKB/TrEMBL
  Hydrolase UniProtKB/TrEMBL
PRINTS CATATPASE UniProtKB/TrEMBL
  CUATPASEI UniProtKB/TrEMBL
PROSITE ATPASE_E1_E2 UniProtKB/TrEMBL
  HMA_1 UniProtKB/TrEMBL
  HMA_2 UniProtKB/TrEMBL
Superfamily-SCOP SSF55008 UniProtKB/TrEMBL
  SSF56784 UniProtKB/TrEMBL
  SSF81653 UniProtKB/TrEMBL
  SSF81665 UniProtKB/TrEMBL
UniProt A0A8C2YL85 ENTREZGENE, UniProtKB/TrEMBL
1 to 36 of 36 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-08-03 Atp7b  ATPase copper transporting beta    ATPase, Cu++ transporting, beta polypeptide  Symbol and/or name change 5135510 APPROVED