ATP2B4 (ATPase plasma membrane Ca2+ transporting 4) - Rat Genome Database

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Gene: ATP2B4 (ATPase plasma membrane Ca2+ transporting 4) Homo sapiens
Analyze
Symbol: ATP2B4
Name: ATPase plasma membrane Ca2+ transporting 4
RGD ID: 1348952
HGNC Page HGNC
Description: Enables several functions, including calmodulin binding activity; enzyme binding activity; and nitric-oxide synthase inhibitor activity. Involved in several processes, including negative regulation of cellular amino acid metabolic process; negative regulation of signal transduction; and positive regulation of protein phosphorylation. Located in T-tubule and Z disc.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ATP2B2; ATPase, Ca++ transporting, plasma membrane 4; DKFZp686G08106; DKFZp686M088; matrix-remodeling-associated protein 1; matrix-remodelling associated 1; MXRA1; plasma membrane calcium ATPase; plasma membrane calcium pump; plasma membrane calcium-transporting ATPase 4; PMCA4; PMCA4b; PMCA4x; sarcolemmal calcium pump
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1203,626,787 - 203,744,081 (+)EnsemblGRCh38hg38GRCh38
GRCh381203,626,832 - 203,744,081 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371203,595,960 - 203,713,209 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361201,862,551 - 201,979,832 (+)NCBINCBI36hg18NCBI36
Build 341200,327,584 - 200,444,864NCBI
Celera1176,726,268 - 176,843,554 (+)NCBI
Cytogenetic Map1q32.1NCBI
HuRef1174,761,519 - 174,878,762 (+)NCBIHuRef
CHM1_11205,019,430 - 205,136,718 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-demecolcine  (EXP)
(-)-epigallocatechin 3-gallate  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-hydroxypropanoic acid  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
4,4'-sulfonyldiphenol  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
acrolein  (EXP)
acrylamide  (EXP)
aflatoxin B1  (EXP)
alpha-pinene  (EXP)
ammonium acetate  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
atrazine  (EXP,ISO)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (ISO)
butan-1-ol  (EXP)
calcium atom  (EXP)
calcium(0)  (EXP)
chlorpyrifos  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper atom  (EXP)
copper(0)  (EXP)
cyclosporin A  (EXP)
dexamethasone  (EXP)
dicrotophos  (EXP)
dioxygen  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
elemental selenium  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
fenofibrate  (EXP)
fenvalerate  (ISO)
flavonoids  (ISO)
formaldehyde  (EXP)
irinotecan  (EXP)
isotretinoin  (EXP)
lead(0)  (EXP)
lead(2+)  (EXP)
lycopene  (ISO)
manganese(II) chloride  (ISO)
medroxyprogesterone acetate  (EXP)
methotrexate  (EXP)
methylseleninic acid  (EXP)
nickel sulfate  (EXP)
ozone  (EXP)
paracetamol  (EXP)
PCB138  (ISO)
perfluorononanoic acid  (EXP)
phenylephrine  (EXP)
pirinixic acid  (ISO)
potassium chromate  (EXP)
progesterone  (EXP)
prostaglandin F2alpha  (EXP)
rac-lactic acid  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
selenium atom  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (ISO)
sulforaphane  (EXP)
sunitinib  (EXP)
temozolomide  (EXP)
trichostatin A  (EXP)
triptonide  (ISO)
valproic acid  (EXP,ISO)
vincristine  (EXP)
zalcitabine  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
calcium ion export  (IDA,ISO)
calcium ion import across plasma membrane  (IC)
calcium ion transmembrane import into cytosol  (IC)
calcium ion transmembrane transport  (IEA,IMP,ISO)
calcium ion transport  (ISO)
cellular calcium ion homeostasis  (IBA,IC,IDA,ISS)
cellular response to acetylcholine  (ISS)
cellular response to epinephrine stimulus  (IDA)
flagellated sperm motility  (ISS)
hippocampus development  (IEA,ISO)
ion transmembrane transport  (TAS)
negative regulation of adenylate cyclase-activating adrenergic receptor signaling pathway involved in heart process  (IDA)
negative regulation of angiogenesis  (IDA)
negative regulation of arginine catabolic process  (IDA)
negative regulation of blood vessel endothelial cell migration  (IDA)
negative regulation of calcineurin-NFAT signaling cascade  (IDA,IMP)
negative regulation of cardiac muscle hypertrophy in response to stress  (IMP)
negative regulation of cellular response to vascular endothelial growth factor stimulus  (IDA)
negative regulation of citrulline biosynthetic process  (IDA)
negative regulation of gene expression  (IDA)
negative regulation of nitric oxide biosynthetic process  (IDA)
negative regulation of nitric oxide mediated signal transduction  (IDA)
negative regulation of nitric-oxide synthase activity  (IDA)
negative regulation of peptidyl-cysteine S-nitrosylation  (NAS)
negative regulation of the force of heart contraction  (IDA)
neural retina development  (IEA,ISO)
positive regulation of cAMP-dependent protein kinase activity  (IDA)
positive regulation of peptidyl-serine phosphorylation  (IDA)
positive regulation of protein localization to plasma membrane  (IDA)
regulation of cardiac conduction  (TAS)
regulation of cell cycle G1/S phase transition  (IMP)
regulation of cytosolic calcium ion concentration  (IBA)
regulation of sodium ion transmembrane transport  (IC)
regulation of transcription by RNA polymerase II  (IMP)
response to hydrostatic pressure  (IMP)
spermatogenesis  (IEA,ISO)
transport across blood-brain barrier  (NAS)
urinary bladder smooth muscle contraction  (ISS)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:1313367   PMID:1531651   PMID:1674727   PMID:2137451   PMID:2963820   PMID:2966397   PMID:7945253   PMID:7989379   PMID:8245032   PMID:8530416   PMID:8634322   PMID:8670083  
PMID:8700162   PMID:9105688   PMID:9182531   PMID:9430700   PMID:9880546   PMID:10737800   PMID:10748016   PMID:11076863   PMID:11152753   PMID:11230166   PMID:11274188   PMID:11591728  
PMID:11751908   PMID:12477932   PMID:12511555   PMID:12540962   PMID:12763866   PMID:12784250   PMID:12944246   PMID:15071553   PMID:15101689   PMID:15123239   PMID:15133509   PMID:15145946  
PMID:15292209   PMID:15489336   PMID:15955804   PMID:16080782   PMID:16216224   PMID:16381901   PMID:16412504   PMID:16735509   PMID:16973504   PMID:16978418   PMID:17242280   PMID:17393022  
PMID:17689535   PMID:17883705   PMID:17957572   PMID:18591664   PMID:18657858   PMID:19034380   PMID:19073225   PMID:19278978   PMID:19287093   PMID:19536175   PMID:19755660   PMID:19946888  
PMID:19996092   PMID:20211863   PMID:20301682   PMID:20379614   PMID:21073872   PMID:21139678   PMID:21167220   PMID:21873635   PMID:22084111   PMID:22480210   PMID:22525089   PMID:22747683  
PMID:22767601   PMID:22810586   PMID:22895189   PMID:23263863   PMID:23266958   PMID:23444010   PMID:23549614   PMID:23602568   PMID:23798571   PMID:23830917   PMID:24189400   PMID:24448801  
PMID:24583174   PMID:25119969   PMID:25147342   PMID:25233416   PMID:25468996   PMID:25690014   PMID:25798335   PMID:25906147   PMID:26116539   PMID:26186194   PMID:26344197   PMID:26448358  
PMID:26618866   PMID:26638075   PMID:26676968   PMID:26729804   PMID:27342126   PMID:27813079   PMID:27880917   PMID:28216081   PMID:28327142   PMID:28514442   PMID:28684310   PMID:28714864  
PMID:28787189   PMID:29042438   PMID:29117863   PMID:29467281   PMID:29487197   PMID:29507755   PMID:30021884   PMID:30194290   PMID:30280653   PMID:30442766   PMID:30639242   PMID:30997501  
PMID:31073040   PMID:31091453   PMID:31594854   PMID:32002807   PMID:32414111   PMID:32860837   PMID:32913203   PMID:32926932   PMID:33060197   PMID:33845483   PMID:33957083   PMID:33961781  
PMID:34079125   PMID:34093590  


Genomics

Comparative Map Data
ATP2B4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1203,626,787 - 203,744,081 (+)EnsemblGRCh38hg38GRCh38
GRCh381203,626,832 - 203,744,081 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371203,595,960 - 203,713,209 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361201,862,551 - 201,979,832 (+)NCBINCBI36hg18NCBI36
Build 341200,327,584 - 200,444,864NCBI
Celera1176,726,268 - 176,843,554 (+)NCBI
Cytogenetic Map1q32.1NCBI
HuRef1174,761,519 - 174,878,762 (+)NCBIHuRef
CHM1_11205,019,430 - 205,136,718 (+)NCBICHM1_1
Atp2b4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391133,630,411 - 133,728,797 (-)NCBIGRCm39mm39
GRCm39 Ensembl1133,627,195 - 133,728,779 (-)Ensembl
GRCm381133,702,674 - 133,801,059 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1133,699,457 - 133,801,041 (-)EnsemblGRCm38mm10GRCm38
MGSCv371135,600,842 - 135,650,098 (-)NCBIGRCm37mm9NCBIm37
MGSCv361135,523,068 - 135,569,692 (-)NCBImm8
Celera1136,319,758 - 136,369,233 (-)NCBICelera
Cytogenetic Map1E4NCBI
cM Map157.95NCBI
Atp2b4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21345,156,137 - 45,255,292 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl1345,156,146 - 45,255,246 (-)Ensembl
Rnor_6.01350,091,644 - 50,153,808 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1350,091,430 - 50,153,823 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01355,157,902 - 55,204,205 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41346,631,205 - 46,697,214 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11346,645,247 - 46,711,257 (-)NCBI
Celera1345,491,969 - 45,537,415 (-)NCBICelera
Cytogenetic Map13q13NCBI
Atp2b4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540639,552,019 - 39,645,694 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540639,552,034 - 39,645,694 (+)NCBIChiLan1.0ChiLan1.0
ATP2B4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11183,524,723 - 183,639,882 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1183,580,773 - 183,639,882 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01179,231,712 - 179,348,759 (+)NCBIMhudiblu_PPA_v0panPan3
ATP2B4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.138321,246 - 420,262 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl38366,656 - 416,952 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha38417,183 - 516,056 (+)NCBI
ROS_Cfam_1.038317,612 - 416,061 (+)NCBI
UMICH_Zoey_3.138309,836 - 412,983 (+)NCBI
UNSW_CanFamBas_1.038703,967 - 803,295 (+)NCBI
UU_Cfam_GSD_1.038918,139 - 1,017,502 (+)NCBI
Atp2b4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934471,711,968 - 71,805,329 (-)NCBI
SpeTri2.0NW_004936567944,825 - 1,039,920 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ATP2B4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl964,336,499 - 64,445,663 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1964,336,354 - 64,445,669 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2970,628,153 - 70,765,686 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ATP2B4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12525,602,857 - 25,716,385 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2525,602,715 - 25,661,553 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366605526,377,416 - 26,491,085 (-)NCBIVero_WHO_p1.0
Atp2b4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248077,201,924 - 7,292,010 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
D1S510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,595,357 - 203,595,547UniSTSGRCh37
GRCh371203,595,375 - 203,595,506UniSTSGRCh37
Build 361201,861,980 - 201,862,170RGDNCBI36
Celera1176,725,697 - 176,725,887RGD
Celera1176,725,715 - 176,725,846UniSTS
Cytogenetic Map1q32.1UniSTS
HuRef1174,760,965 - 174,761,151UniSTS
HuRef1174,760,983 - 174,761,110UniSTS
Marshfield Genetic Map1218.46UniSTS
Marshfield Genetic Map1218.46RGD
Genethon Genetic Map1223.0UniSTS
TNG Radiation Hybrid Map133371.0UniSTS
deCODE Assembly Map1204.35UniSTS
Stanford-G3 RH Map17866.0UniSTS
GeneMap99-GB4 RH Map1673.93UniSTS
Whitehead-RH Map1831.4UniSTS
Whitehead-YAC Contig Map1 UniSTS
GeneMap99-G3 RH Map17822.0UniSTS
D1S387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,686,680 - 203,686,859UniSTSGRCh37
Build 361201,953,303 - 201,953,482RGDNCBI36
Celera1176,817,024 - 176,817,203RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,852,226 - 174,852,405UniSTS
AL034138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,918 - 203,713,099UniSTSGRCh37
Build 361201,979,541 - 201,979,722RGDNCBI36
Celera1176,843,263 - 176,843,444RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,471 - 174,878,652UniSTS
SHGC-56960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,702,579 - 203,702,702UniSTSGRCh37
Build 361201,969,202 - 201,969,325RGDNCBI36
Celera1176,832,924 - 176,833,047RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,868,134 - 174,868,257UniSTS
TNG Radiation Hybrid Map133348.0UniSTS
RH64618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,711,301 - 203,711,440UniSTSGRCh37
Build 361201,977,924 - 201,978,063RGDNCBI36
Celera1176,841,646 - 176,841,785RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,876,854 - 174,876,993UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
NCBI RH Map11743.5UniSTS
RH63844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,621 - 203,712,772UniSTSGRCh37
Build 361201,979,244 - 201,979,395RGDNCBI36
Celera1176,842,966 - 176,843,117RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,174 - 174,878,325UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map11743.5UniSTS
G19696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,883 - 203,713,033UniSTSGRCh37
Build 361201,979,506 - 201,979,656RGDNCBI36
Celera1176,843,228 - 176,843,378RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,436 - 174,878,586UniSTS
A001V38  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,883 - 203,713,033UniSTSGRCh37
Build 361201,979,506 - 201,979,656RGDNCBI36
Celera1176,843,228 - 176,843,378RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,436 - 174,878,586UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
NCBI RH Map11743.5UniSTS
SHGC-76196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,711,140 - 203,711,255UniSTSGRCh37
Build 361201,977,763 - 201,977,878RGDNCBI36
Celera1176,841,485 - 176,841,600RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,876,693 - 174,876,808UniSTS
TNG Radiation Hybrid Map133326.0UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
NCBI RH Map11744.7UniSTS
SHGC-76187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,544 - 203,712,749UniSTSGRCh37
Build 361201,979,167 - 201,979,372RGDNCBI36
Celera1176,842,889 - 176,843,094RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,097 - 174,878,302UniSTS
TNG Radiation Hybrid Map133322.0UniSTS
GeneMap99-GB4 RH Map1673.73UniSTS
D1S2376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,712,867 - 203,713,150UniSTSGRCh37
Build 361201,979,490 - 201,979,773RGDNCBI36
Celera1176,843,212 - 176,843,495RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,878,420 - 174,878,703UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
Whitehead-RH Map1831.4UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map11744.7UniSTS
RH64645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,711,105 - 203,711,345UniSTSGRCh37
Build 361201,977,728 - 201,977,968RGDNCBI36
Celera1176,841,450 - 176,841,690RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,876,658 - 174,876,898UniSTS
GeneMap99-GB4 RH Map1674.01UniSTS
NCBI RH Map11743.5UniSTS
SHGC-12393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371203,709,056 - 203,709,399UniSTSGRCh37
Build 361201,975,679 - 201,976,022RGDNCBI36
Celera1176,839,401 - 176,839,744RGD
Cytogenetic Map1q32.1UniSTS
HuRef1174,874,609 - 174,874,952UniSTS
Stanford-G3 RH Map17857.0UniSTS
Whitehead-YAC Contig Map1 UniSTS
GeneMap99-G3 RH Map17813.0UniSTS
SHGC-76189  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q32.1UniSTS
TNG Radiation Hybrid Map133335.0UniSTS
GeneMap99-GB4 RH Map1673.83UniSTS
NCBI RH Map11743.5UniSTS
D1S510  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q32.1UniSTS
TNG Radiation Hybrid Map133371.0UniSTS
Stanford-G3 RH Map17866.0UniSTS
GeneMap99-G3 RH Map17822.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:9943
Count of miRNA genes:1112
Interacting mature miRNAs:1333
Transcripts:ENST00000341360, ENST00000356729, ENST00000357681, ENST00000367218, ENST00000367219, ENST00000391954, ENST00000458092, ENST00000466407, ENST00000484746
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1 2
Medium 2147 2693 1510 407 1283 266 3630 1389 3161 309 1428 1580 154 1204 2069 4
Low 290 298 215 216 617 199 726 807 570 109 30 33 21 1 719 2 1
Below cutoff 2 1 50 3 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001001396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC114402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL513343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL601702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL706212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW888226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC140774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF740130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF985985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537444 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR936708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DN997129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ201780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ201781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M25874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M83363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U42026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U42061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U42062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U42378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000341360   ⟹   ENSP00000340930
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,682,809 - 203,740,319 (+)Ensembl
RefSeq Acc Id: ENST00000356729   ⟹   ENSP00000349165
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,723,963 - 203,733,632 (+)Ensembl
RefSeq Acc Id: ENST00000357681   ⟹   ENSP00000350310
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,626,832 - 203,744,081 (+)Ensembl
RefSeq Acc Id: ENST00000367218   ⟹   ENSP00000356187
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,626,787 - 203,744,079 (+)Ensembl
RefSeq Acc Id: ENST00000458092   ⟹   ENSP00000391150
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,723,897 - 203,728,310 (+)Ensembl
RefSeq Acc Id: ENST00000466407
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,723,961 - 203,727,754 (+)Ensembl
RefSeq Acc Id: ENST00000484746   ⟹   ENSP00000433577
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1203,727,468 - 203,744,080 (+)Ensembl
RefSeq Acc Id: NM_001001396   ⟹   NP_001001396
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,626,832 - 203,744,081 (+)NCBI
GRCh371203,595,915 - 203,713,209 (+)NCBI
Build 361201,862,551 - 201,979,832 (+)NCBI Archive
HuRef1174,761,519 - 174,878,762 (+)NCBI
CHM1_11205,019,430 - 205,136,718 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001365783   ⟹   NP_001352712
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,626,832 - 203,733,629 (+)NCBI
RefSeq Acc Id: NM_001365784   ⟹   NP_001352713
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,627,937 - 203,733,629 (+)NCBI
RefSeq Acc Id: NM_001684   ⟹   NP_001675
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,626,832 - 203,744,081 (+)NCBI
GRCh371203,595,915 - 203,713,209 (+)NCBI
Build 361201,862,551 - 201,979,832 (+)NCBI Archive
HuRef1174,761,519 - 174,878,762 (+)NCBI
CHM1_11205,019,430 - 205,136,718 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001001396   ⟸   NM_001001396
- Peptide Label: isoform 4a
- UniProtKB: P23634 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001675   ⟸   NM_001684
- Peptide Label: isoform 4b
- UniProtKB: P23634 (UniProtKB/Swiss-Prot),   A0A024R968 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001352712   ⟸   NM_001365783
- Peptide Label: isoform 4c
RefSeq Acc Id: NP_001352713   ⟸   NM_001365784
- Peptide Label: isoform 4c
RefSeq Acc Id: ENSP00000391150   ⟸   ENST00000458092
RefSeq Acc Id: ENSP00000433577   ⟸   ENST00000484746
RefSeq Acc Id: ENSP00000356187   ⟸   ENST00000367218
RefSeq Acc Id: ENSP00000340930   ⟸   ENST00000341360
RefSeq Acc Id: ENSP00000349165   ⟸   ENST00000356729
RefSeq Acc Id: ENSP00000350310   ⟸   ENST00000357681
Promoters
RGD ID:6785140
Promoter ID:HG_KWN:6908
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000356729,   ENST00000357681,   ENST00000367218,   ENST00000367219,   ENST00000391954
Position:
Human AssemblyChrPosition (strand)Source
Build 361201,861,516 - 201,862,617 (+)MPROMDB
RGD ID:6785139
Promoter ID:HG_KWN:6909
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   K562
Transcripts:ENST00000341360,   UC009XAQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361201,917,881 - 201,918,772 (+)MPROMDB
RGD ID:6858688
Promoter ID:EPDNEW_H2484
Type:initiation region
Name:ATP2B4_1
Description:ATPase plasma membrane Ca2+ transporting 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2485  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,626,832 - 203,626,892EPDNEW
RGD ID:6858640
Promoter ID:EPDNEW_H2485
Type:initiation region
Name:ATP2B4_2
Description:ATPase plasma membrane Ca2+ transporting 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2484  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381203,627,105 - 203,627,165EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001001396.2(ATP2B4):c.-464-21082A>G single nucleotide variant Lung cancer [RCV000090370] Chr1:203661660 [GRCh38]
Chr1:203630788 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3 copy number gain See cases [RCV000051857] Chr1:187143981..224299417 [GRCh38]
Chr1:187113113..224487119 [GRCh37]
Chr1:185379736..222553742 [NCBI36]
Chr1:1q31.1-42.11
pathogenic
NM_001001396.2(ATP2B4):c.466C>T (p.Leu156Phe) single nucleotide variant Malignant melanoma [RCV000064465] Chr1:203699534 [GRCh38]
Chr1:203668662 [GRCh37]
Chr1:201935285 [NCBI36]
Chr1:1q32.1
not provided
NM_001001396.2(ATP2B4):c.2027C>T (p.Pro676Leu) single nucleotide variant Malignant melanoma [RCV000064466] Chr1:203711104 [GRCh38]
Chr1:203680232 [GRCh37]
Chr1:201946855 [NCBI36]
Chr1:1q32.1
not provided
NM_001001396.2(ATP2B4):c.2799C>T (p.Ile933=) single nucleotide variant Malignant melanoma [RCV000064467] Chr1:203721397 [GRCh38]
Chr1:203690525 [GRCh37]
Chr1:201957148 [NCBI36]
Chr1:1q32.1
not provided
NM_001001396.2(ATP2B4):c.760C>T (p.Pro254Ser) single nucleotide variant Malignant melanoma [RCV000060053] Chr1:203700316 [GRCh38]
Chr1:203669444 [GRCh37]
Chr1:201936067 [NCBI36]
Chr1:1q32.1
not provided
NM_001684.5(ATP2B4):c.999C>A (p.Asp333Glu) single nucleotide variant Malignant tumor of prostate [RCV000149010] Chr1:203703713 [GRCh38]
Chr1:203672841 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3 copy number gain See cases [RCV000240137] Chr1:197811907..228997888 [GRCh37]
Chr1:1q31.3-42.13
pathogenic
NM_001684.5(ATP2B4):c.2548G>A (p.Val850Ile) single nucleotide variant not provided [RCV000415896] Chr1:203720690 [GRCh38]
Chr1:203689818 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3 copy number gain See cases [RCV000449172] Chr1:195483439..249213000 [GRCh37]
Chr1:1q31.3-44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q32.1(chr1:203681085-203687130)x1 copy number loss not provided [RCV000736834] Chr1:203681085..203687130 [GRCh37]
Chr1:1q32.1
benign
GRCh37/hg19 1q32.1(chr1:203681255-203685886)x1 copy number loss not provided [RCV000736835] Chr1:203681255..203685886 [GRCh37]
Chr1:1q32.1
benign
GRCh37/hg19 1q32.1(chr1:203681255-203687130)x1 copy number loss not provided [RCV000736836] Chr1:203681255..203687130 [GRCh37]
Chr1:1q32.1
benign
GRCh37/hg19 1q25.3-41(chr1:185644663-221698833)x3 copy number gain not provided [RCV000749265] Chr1:185644663..221698833 [GRCh37]
Chr1:1q25.3-41
pathogenic
NM_001684.5(ATP2B4):c.3133-10T>C single nucleotide variant not provided [RCV000874024] Chr1:203727385 [GRCh38]
Chr1:203696513 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.1839A>T (p.Pro613=) single nucleotide variant not provided [RCV000874154] Chr1:203710916 [GRCh38]
Chr1:203680044 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.1025T>C (p.Val342Ala) single nucleotide variant not provided [RCV000873606] Chr1:203703739 [GRCh38]
Chr1:203672867 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.19C>T (p.Arg7Cys) single nucleotide variant not provided [RCV000873715] Chr1:203683224 [GRCh38]
Chr1:203652352 [GRCh37]
Chr1:1q32.1
likely benign
NM_001684.5(ATP2B4):c.1545C>T (p.Thr515=) single nucleotide variant not provided [RCV000873789] Chr1:203708092 [GRCh38]
Chr1:203677220 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.19C>A (p.Arg7Ser) single nucleotide variant not provided [RCV000875374] Chr1:203683224 [GRCh38]
Chr1:203652352 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.863G>T (p.Gly288Val) single nucleotide variant not provided [RCV000875375] Chr1:203700885 [GRCh38]
Chr1:203670013 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.2819A>G (p.Lys940Arg) single nucleotide variant not provided [RCV000876546] Chr1:203722484 [GRCh38]
Chr1:203691612 [GRCh37]
Chr1:1q32.1
likely benign
NM_001684.5(ATP2B4):c.1981G>A (p.Glu661Lys) single nucleotide variant not provided [RCV000877233] Chr1:203711058 [GRCh38]
Chr1:203680186 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.3291G>A (p.Leu1097=) single nucleotide variant not provided [RCV000878742] Chr1:203727553 [GRCh38]
Chr1:203696681 [GRCh37]
Chr1:1q32.1
likely benign
NM_001684.5(ATP2B4):c.1968T>C (p.Asn656=) single nucleotide variant not provided [RCV000873636] Chr1:203711045 [GRCh38]
Chr1:203680173 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.3291G>T (p.Leu1097=) single nucleotide variant not provided [RCV000876119] Chr1:203727553 [GRCh38]
Chr1:203696681 [GRCh37]
Chr1:1q32.1
benign
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44
pathogenic
GRCh37/hg19 1q32.1(chr1:203658206-203938853)x3 copy number gain not provided [RCV000848646] Chr1:203658206..203938853 [GRCh37]
Chr1:1q32.1
uncertain significance
GRCh37/hg19 1q31.3-32.2(chr1:194356425-210988710)x3 copy number gain not provided [RCV001249273] Chr1:194356425..210988710 [GRCh37]
Chr1:1q31.3-32.2
not provided
NM_001684.5(ATP2B4):c.2599-5G>T single nucleotide variant not provided [RCV000996108] Chr1:203721192 [GRCh38]
Chr1:203690320 [GRCh37]
Chr1:1q32.1
uncertain significance
NM_001684.5(ATP2B4):c.423T>C (p.Asp141=) single nucleotide variant not provided [RCV000910182] Chr1:203699491 [GRCh38]
Chr1:203668619 [GRCh37]
Chr1:1q32.1
likely benign
NM_001684.5(ATP2B4):c.3219C>T (p.Ala1073=) single nucleotide variant not provided [RCV000875240] Chr1:203727481 [GRCh38]
Chr1:203696609 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.3158C>T (p.Ser1053Phe) single nucleotide variant not provided [RCV000873563] Chr1:203727420 [GRCh38]
Chr1:203696548 [GRCh37]
Chr1:1q32.1
benign
NM_001684.5(ATP2B4):c.1665T>C (p.Asn555=) single nucleotide variant not provided [RCV000873635] Chr1:203709408 [GRCh38]
Chr1:203678536 [GRCh37]
Chr1:1q32.1
benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance
NM_001684.5(ATP2B4):c.1826G>C (p.Gly609Ala) single nucleotide variant not provided [RCV001491834] Chr1:203710903 [GRCh38]
Chr1:203680031 [GRCh37]
Chr1:1q32.1
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:817 AgrOrtholog
COSMIC ATP2B4 COSMIC
Ensembl Genes ENSG00000058668 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000340930 UniProtKB/Swiss-Prot
  ENSP00000349165 UniProtKB/TrEMBL
  ENSP00000350310 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000356187 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000391150 UniProtKB/TrEMBL
  ENSP00000433577 UniProtKB/TrEMBL
Ensembl Transcript ENST00000341360 UniProtKB/Swiss-Prot
  ENST00000356729 UniProtKB/TrEMBL
  ENST00000357681 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000367218 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000458092 UniProtKB/TrEMBL
  ENST00000484746 UniProtKB/TrEMBL
Gene3D-CATH 3.40.1110.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.1000 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000058668 GTEx
HGNC ID HGNC:817 ENTREZGENE
Human Proteome Map ATP2B4 Human Proteome Map
InterPro ATP2B2 UniProtKB/TrEMBL
  ATP_Ca_trans_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_cation-transptr_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_cation-transptr_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_cyto_dom_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_P_site UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_TM_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-typ_transduc_dom_A_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HAD-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HAD_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-type_ATPase_IIB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P_typ_ATPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P_typ_ATPase_HD_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:493 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 493 ENTREZGENE
OMIM 108732 OMIM
PANTHER PTHR24093:SF377 UniProtKB/TrEMBL
Pfam ATP_Ca_trans_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cation_ATPase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cation_ATPase_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25110 PharmGKB
PROSITE ATPASE_E1_E2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Cation_ATPase_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56784 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81653 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81660 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81665 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
TIGRFAMs ATPase-IIB_Ca UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_P-type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R968 ENTREZGENE, UniProtKB/TrEMBL
  A1X4Q1_HUMAN UniProtKB/TrEMBL
  A1X4Q2_HUMAN UniProtKB/TrEMBL
  A7E2D8_HUMAN UniProtKB/TrEMBL
  AT2B4_HUMAN UniProtKB/Swiss-Prot
  H0YDG5_HUMAN UniProtKB/TrEMBL
  H7BY13_HUMAN UniProtKB/TrEMBL
  H7BZS8_HUMAN UniProtKB/TrEMBL
  P23634 ENTREZGENE
UniProt Secondary B1APW5 UniProtKB/Swiss-Prot
  B1APW6 UniProtKB/Swiss-Prot
  Q13450 UniProtKB/Swiss-Prot
  Q13452 UniProtKB/Swiss-Prot
  Q13455 UniProtKB/Swiss-Prot
  Q16817 UniProtKB/Swiss-Prot
  Q7Z3S1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-01 ATP2B4  ATPase plasma membrane Ca2+ transporting 4  MXRA1~withdrawn  matrix-remodelling associated 1  Data Merged 737654 PROVISIONAL
2016-02-29 MXRA1~withdrawn  matrix-remodelling associated 1  MXRA1    Symbol and/or name change 5135510 APPROVED
2016-02-16 ATP2B4  ATPase plasma membrane Ca2+ transporting 4    ATPase, Ca++ transporting, plasma membrane 4  Symbol and/or name change 5135510 APPROVED
2011-08-16 ATP2B4  ATPase, Ca++ transporting, plasma membrane 4  ATP2B4  ATPase, Ca++ transporting, plasma membrane 4  Symbol and/or name change 5135510 APPROVED