PTPRJ (protein tyrosine phosphatase receptor type J) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: PTPRJ (protein tyrosine phosphatase receptor type J) Homo sapiens
Analyze
Symbol: PTPRJ
Name: protein tyrosine phosphatase receptor type J
RGD ID: 736433
HGNC Page HGNC
Description: Enables several functions, including beta-catenin binding activity; delta-catenin binding activity; and gamma-catenin binding activity. Involved in several processes, including negative regulation of signal transduction; positive regulation of focal adhesion assembly; and positive regulation of protein kinase B signaling. Located in cell surface; cell-cell junction; and immunological synapse. Implicated in colorectal cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CD148; CD148 antigen; density-enhanced phosphatase 1; DEP-1; DEP1; HPTP eta; HPTPeta; human density enhanced phosphatase-1; protein tyrosine phosphatase, receptor type, J polypeptide; protein-tyrosine phosphatase eta; protein-tyrosine phosphatase receptor type J; R-PTP-ETA; R-PTP-J; receptor-type tyrosine-protein phosphatase eta; SCC1; susceptibility to colon cancer 1, mouse, homolog of
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 Ensembl1147,980,559 - 48,170,839 (+)EnsemblGRCh38hg38GRCh38
GRCh381147,980,504 - 48,170,839 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371148,002,111 - 48,192,391 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361147,958,686 - 48,148,970 (+)NCBINCBI36hg18NCBI36
Build 341147,958,688 - 48,146,246NCBI
Celera1148,154,504 - 48,344,533 (+)NCBI
Cytogenetic Map11p11.2NCBI
HuRef1147,683,384 - 47,903,543 (+)NCBIHuRef
CHM1_11148,001,881 - 48,191,974 (+)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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
B cell differentiation  (ISS)
blood coagulation  (ISO)
calcium-mediated signaling using intracellular calcium source  (ISS)
contact inhibition  (NAS)
cytokine-mediated signaling pathway  (TAS)
dephosphorylation  (IEA)
glucose homeostasis  (ISO)
heart development  (ISO)
negative regulation of cell growth  (IDA)
negative regulation of cell migration  (IDA)
negative regulation of cell population proliferation  (IDA)
negative regulation of epidermal growth factor receptor signaling pathway  (IMP)
negative regulation of insulin receptor signaling pathway  (ISO)
negative regulation of MAP kinase activity  (IBA,IDA)
negative regulation of platelet-derived growth factor receptor signaling pathway  (IDA)
negative regulation of protein kinase B signaling  (IMP)
negative regulation of signaling receptor activity  (ISO)
negative regulation of T cell receptor signaling pathway  (IDA,IMP)
negative regulation of vascular permeability  (IDA)
oligodendrocyte differentiation  (ISO)
peptidyl-tyrosine dephosphorylation  (IDA,IEA,IMP)
peptidyl-tyrosine dephosphorylation involved in inactivation of protein kinase activity  (ISO)
platelet-derived growth factor receptor signaling pathway  (IMP)
positive chemotaxis  (IDA)
positive regulation of cell adhesion  (IMP)
positive regulation of cell-matrix adhesion  (ISO)
positive regulation of Fc-gamma receptor signaling pathway involved in phagocytosis  (ISS)
positive regulation of focal adhesion assembly  (IMP)
positive regulation of macrophage chemotaxis  (ISO)
positive regulation of MAPK cascade  (ISS)
positive regulation of peptidyl-tyrosine phosphorylation  (ISS)
positive regulation of platelet activation  (ISO)
positive regulation of protein kinase B signaling  (IMP)
positive regulation of tumor necrosis factor production  (ISS)
protein dephosphorylation  (IBA,IEA)
regulation of cell adhesion  (IMP)
T cell receptor signaling pathway  (TAS)
vasculogenesis  (ISO)

Cellular Component

References

Additional References at PubMed
PMID:7937872   PMID:7994032   PMID:9115287   PMID:9531590   PMID:9759839   PMID:9780142   PMID:10473595   PMID:10599888   PMID:10648410   PMID:10821867   PMID:10914487   PMID:11259588  
PMID:11526512   PMID:12062403   PMID:12089527   PMID:12370829   PMID:12403354   PMID:12475979   PMID:12477932   PMID:12685844   PMID:12771128   PMID:12913111   PMID:14709717   PMID:15123617  
PMID:15231692   PMID:15378013   PMID:15384144   PMID:15978577   PMID:16000320   PMID:16335952   PMID:16582570   PMID:16682945   PMID:16893970   PMID:18029348   PMID:18348712   PMID:18603590  
PMID:18843023   PMID:18854154   PMID:18936167   PMID:19056867   PMID:19122201   PMID:19124506   PMID:19167335   PMID:19332538   PMID:19413345   PMID:19494114   PMID:19672627   PMID:19836242  
PMID:19922411   PMID:20139419   PMID:20301390   PMID:20379614   PMID:20823296   PMID:20881960   PMID:21036128   PMID:21091576   PMID:21262971   PMID:21304107   PMID:21502573   PMID:21543337  
PMID:21706016   PMID:21813734   PMID:21873635   PMID:22076464   PMID:22268729   PMID:22308318   PMID:22438257   PMID:22564856   PMID:22677127   PMID:22815804   PMID:23341091   PMID:23376485  
PMID:23533145   PMID:23563607   PMID:23650535   PMID:24016860   PMID:24027763   PMID:24357727   PMID:24412244   PMID:24583284   PMID:25173106   PMID:25386896   PMID:25412306   PMID:25468996  
PMID:25634668   PMID:25640309   PMID:25672645   PMID:25772245   PMID:25791119   PMID:26063811   PMID:26186194   PMID:26248682   PMID:26694178   PMID:26760575   PMID:26871468   PMID:27309885  
PMID:27880917   PMID:28052032   PMID:28316102   PMID:28319085   PMID:28514442   PMID:28611215   PMID:28823811   PMID:28926625   PMID:29117863   PMID:29507755   PMID:29762926   PMID:30021884  
PMID:30591527   PMID:30639242   PMID:30661225   PMID:31715329   PMID:32513696   PMID:33455071   PMID:33784491   PMID:33845483   PMID:33961781   PMID:34079125   PMID:34709727  


Genomics

Comparative Map Data
PTPRJ
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1147,980,559 - 48,170,839 (+)EnsemblGRCh38hg38GRCh38
GRCh381147,980,504 - 48,170,839 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371148,002,111 - 48,192,391 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361147,958,686 - 48,148,970 (+)NCBINCBI36hg18NCBI36
Build 341147,958,688 - 48,146,246NCBI
Celera1148,154,504 - 48,344,533 (+)NCBI
Cytogenetic Map11p11.2NCBI
HuRef1147,683,384 - 47,903,543 (+)NCBIHuRef
CHM1_11148,001,881 - 48,191,974 (+)NCBICHM1_1
Ptprj
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39290,260,100 - 90,411,102 (-)NCBIGRCm39mm39
GRCm39 Ensembl290,260,098 - 90,410,991 (-)Ensembl
GRCm38290,429,756 - 90,580,694 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl290,429,754 - 90,580,647 (-)EnsemblGRCm38mm10GRCm38
MGSCv37290,269,913 - 90,420,804 (-)NCBIGRCm37mm9NCBIm37
MGSCv36290,233,731 - 90,381,407 (-)NCBImm8
Celera291,810,313 - 91,967,158 (-)NCBICelera
Cytogenetic Map2E1NCBI
cM Map250.19NCBI
Ptprj
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2376,405,917 - 76,561,842 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl376,405,927 - 76,562,260 (-)Ensembl
Rnor_6.0379,233,519 - 79,390,956 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl379,233,525 - 79,390,956 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0385,947,682 - 86,099,287 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4374,796,764 - 74,935,540 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1374,693,135 - 74,831,912 (-)NCBI
Celera375,621,921 - 75,777,388 (-)NCBICelera
Cytogenetic Map3q24NCBI
Ptprj
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955422399,357 - 443,054 (-)EnsemblChiLan1.0
ChiLan1.0NW_004955422396,266 - 438,792 (-)NCBIChiLan1.0ChiLan1.0
PTPRJ
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11148,518,844 - 48,672,844 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1148,613,761 - 48,670,494 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01147,941,134 - 48,130,538 (+)NCBIMhudiblu_PPA_v0panPan3
PTPRJ
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11841,586,262 - 41,635,386 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1841,586,112 - 41,635,308 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1840,315,308 - 40,366,352 (-)NCBI
ROS_Cfam_1.01842,238,579 - 42,289,675 (-)NCBI
ROS_Cfam_1.0 Ensembl1842,238,586 - 42,285,426 (-)Ensembl
UMICH_Zoey_3.11841,727,516 - 41,778,615 (-)NCBI
UNSW_CanFamBas_1.01841,280,105 - 41,331,461 (-)NCBI
UU_Cfam_GSD_1.01842,009,997 - 42,061,288 (-)NCBI
Ptprj
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494719,050,113 - 19,123,158 (-)NCBI
SpeTri2.0NW_0049365621,161,764 - 1,234,800 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PTPRJ
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl214,548,425 - 14,726,715 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1214,548,489 - 14,724,823 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2215,632,255 - 16,007,397 (-)NCBISscrofa10.2Sscrofa10.2susScr3
PTPRJ
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1117,137,896 - 17,328,836 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl117,135,907 - 17,328,590 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666038114,433,977 - 114,653,560 (-)NCBIVero_WHO_p1.0
Ptprj
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624767942,786 - 1,051,112 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
D11S1350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,180,657 - 48,180,820UniSTSGRCh37
GRCh371148,180,632 - 48,180,820UniSTSGRCh37
Build 361148,137,208 - 48,137,396RGDNCBI36
Celera1148,332,727 - 48,332,906UniSTS
Celera1148,332,700 - 48,332,906RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,891,752 - 47,891,966UniSTS
HuRef1147,891,779 - 47,891,966UniSTS
Marshfield Genetic Map1158.4RGD
Marshfield Genetic Map1158.4UniSTS
Genethon Genetic Map1162.6UniSTS
deCODE Assembly Map1163.81UniSTS
Whitehead-RH Map11182.8UniSTS
NCBI RH Map11367.8UniSTS
D11S1784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,022,843 - 48,022,987UniSTSGRCh37
Build 361147,979,419 - 47,979,563RGDNCBI36
Celera1148,175,237 - 48,175,381RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,733,033 - 47,733,177UniSTS
Marshfield Genetic Map1158.4RGD
Marshfield Genetic Map1158.4UniSTS
Genethon Genetic Map1163.1UniSTS
deCODE Assembly Map1163.81UniSTS
Whitehead-YAC Contig Map11 UniSTS
SHGC-17236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,134,437 - 48,134,566UniSTSGRCh37
Build 361148,091,013 - 48,091,142RGDNCBI36
Celera1148,286,517 - 48,286,646RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,845,362 - 47,845,491UniSTS
Stanford-G3 RH Map112220.0UniSTS
NCBI RH Map11348.5UniSTS
GeneMap99-G3 RH Map112220.0UniSTS
D11S1225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,080,970 - 48,081,245UniSTSGRCh37
Build 361148,037,546 - 48,037,821RGDNCBI36
Celera1148,233,363 - 48,233,638RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,791,146 - 47,791,421UniSTS
RH17993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,189,266 - 48,189,422UniSTSGRCh37
Build 361148,145,842 - 48,145,998RGDNCBI36
Celera1148,341,407 - 48,341,563RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,900,420 - 47,900,576UniSTS
RH79671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,062,801 - 48,062,997UniSTSGRCh37
Build 361148,019,377 - 48,019,573RGDNCBI36
Celera1148,215,178 - 48,215,374RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,772,987 - 47,773,183UniSTS
RH45248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,132,170 - 48,132,390UniSTSGRCh37
Build 361148,088,746 - 48,088,966RGDNCBI36
Celera1148,284,252 - 48,284,472RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,843,099 - 47,843,319UniSTS
PMC151692P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,185,065 - 48,185,168UniSTSGRCh37
Build 361148,141,641 - 48,141,744RGDNCBI36
Celera1148,337,158 - 48,337,261RGD
HuRef1147,896,218 - 47,896,321UniSTS
PTPRJ_2541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,189,028 - 48,189,866UniSTSGRCh37
Build 361148,145,604 - 48,146,442RGDNCBI36
Celera1148,341,169 - 48,342,007RGD
HuRef1147,900,182 - 47,901,020UniSTS
SHGC-34210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,191,989 - 48,192,117UniSTSGRCh37
Build 361148,148,565 - 48,148,693RGDNCBI36
Celera1148,344,127 - 48,344,255RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,903,137 - 47,903,265UniSTS
TNG Radiation Hybrid Map1122998.0UniSTS
Stanford-G3 RH Map112229.0UniSTS
Whitehead-RH Map11169.3UniSTS
NCBI RH Map11350.5UniSTS
GeneMap99-G3 RH Map112229.0UniSTS
D11S4682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,152,163 - 48,152,302UniSTSGRCh37
Build 361148,108,739 - 48,108,878RGDNCBI36
Celera1148,304,247 - 48,304,386RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,863,092 - 47,863,231UniSTS
Stanford-G3 RH Map112242.0UniSTS
NCBI RH Map11355.9UniSTS
GeneMap99-G3 RH Map112242.0UniSTS
WI-18182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,013,285 - 48,013,434UniSTSGRCh37
Build 361147,969,861 - 47,970,010RGDNCBI36
Celera1148,165,680 - 48,165,829RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,723,475 - 47,723,624UniSTS
Whitehead-RH Map11170.5UniSTS
NCBI RH Map11345.6UniSTS
D11S4544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371148,105,526 - 48,105,686UniSTSGRCh37
Build 361148,062,102 - 48,062,262RGDNCBI36
Celera1148,257,919 - 48,258,079RGD
Cytogenetic Map11p11.2UniSTS
HuRef1147,815,679 - 47,815,839UniSTS
Stanford-G3 RH Map112216.0UniSTS
NCBI RH Map11347.8UniSTS
ha1563  
Human AssemblyChrPosition (strand)SourceJBrowse
HuRef1147,805,284 - 47,805,431UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR328hsa-miR-328-3pMirtarbaseexternal_infoqRT-PCR//Western blotFunctional MTI22564856
MIR328hsa-miR-328-3pOncomiRDBexternal_infoNANA22564856

Predicted Target Of
Summary Value
Count of predictions:1179
Count of miRNA genes:756
Interacting mature miRNAs:855
Transcripts:ENST00000418331, ENST00000440289, ENST00000526550, ENST00000527026, ENST00000527952, ENST00000534219
Prediction methods:Miranda, Rnahybrid, Targetscan
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
Medium 709 711 1040 196 1296 87 885 53 1172 191 343 1376 118 31 598 2
Low 1730 2223 681 426 622 376 3408 2018 2555 223 1115 233 56 1 1173 2127 4 2
Below cutoff 57 5 2 30 2 63 126 7 5 2 4 1 63

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001098503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_930883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC026975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI218139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL359057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC019824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D37781 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR007037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF219146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U10886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000418331   ⟹   ENSP00000400010
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,559 - 48,170,839 (+)Ensembl
RefSeq Acc Id: ENST00000440289   ⟹   ENSP00000409733
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,580 - 48,132,720 (+)Ensembl
RefSeq Acc Id: ENST00000526550
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1148,044,804 - 48,121,147 (+)Ensembl
RefSeq Acc Id: ENST00000527026
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1148,145,078 - 48,149,866 (+)Ensembl
RefSeq Acc Id: ENST00000527952   ⟹   ENSP00000435618
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,727 - 48,123,700 (+)Ensembl
RefSeq Acc Id: ENST00000534219   ⟹   ENSP00000432686
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,727 - 48,121,247 (+)Ensembl
RefSeq Acc Id: ENST00000613246   ⟹   ENSP00000477933
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,558 - 48,170,841 (+)Ensembl
RefSeq Acc Id: ENST00000615445   ⟹   ENSP00000479342
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1147,980,569 - 48,167,762 (+)Ensembl
RefSeq Acc Id: NM_001098503   ⟹   NP_001091973
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,559 - 48,132,720 (+)NCBI
GRCh371148,002,101 - 48,192,394 (+)NCBI
Build 361147,958,686 - 48,110,844 (+)NCBI Archive
HuRef1147,683,384 - 47,903,543 (+)ENTREZGENE
CHM1_11148,001,881 - 48,153,874 (+)NCBI
Sequence:
RefSeq Acc Id: NM_002843   ⟹   NP_002834
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,559 - 48,170,839 (+)NCBI
GRCh371148,002,101 - 48,192,394 (+)NCBI
Build 361147,958,686 - 48,148,970 (+)NCBI Archive
HuRef1147,683,384 - 47,903,543 (+)ENTREZGENE
CHM1_11148,001,881 - 48,191,974 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018083   ⟹   XP_016873572
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,563 - 48,170,839 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018084   ⟹   XP_016873573
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381148,013,118 - 48,170,839 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018085   ⟹   XP_016873574
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,556 - 48,170,839 (+)NCBI
Sequence:
RefSeq Acc Id: XR_930883
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,504 - 48,163,553 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002834   ⟸   NM_002843
- Peptide Label: isoform 1 precursor
- UniProtKB: Q12913 (UniProtKB/Swiss-Prot),   Q9NPR5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001091973   ⟸   NM_001098503
- Peptide Label: isoform 2 precursor
- UniProtKB: Q12913 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016873574   ⟸   XM_017018085
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016873572   ⟸   XM_017018083
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016873573   ⟸   XM_017018084
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000409733   ⟸   ENST00000440289
RefSeq Acc Id: ENSP00000432686   ⟸   ENST00000534219
RefSeq Acc Id: ENSP00000477933   ⟸   ENST00000613246
RefSeq Acc Id: ENSP00000400010   ⟸   ENST00000418331
RefSeq Acc Id: ENSP00000479342   ⟸   ENST00000615445
RefSeq Acc Id: ENSP00000435618   ⟸   ENST00000527952
Promoters
RGD ID:6789280
Promoter ID:HG_KWN:12827
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001098503,   NM_002843
Position:
Human AssemblyChrPosition (strand)Source
Build 361147,958,586 - 47,959,086 (+)MPROMDB
RGD ID:7220285
Promoter ID:EPDNEW_H15888
Type:initiation region
Name:PTPRJ_1
Description:protein tyrosine phosphatase, receptor type J
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15889  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,559 - 47,980,619EPDNEW
RGD ID:7220287
Promoter ID:EPDNEW_H15889
Type:initiation region
Name:PTPRJ_2
Description:protein tyrosine phosphatase, receptor type J
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15888  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381147,980,678 - 47,980,738EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_002843.4(PTPRJ):c.640C>T (p.Arg214Cys) single nucleotide variant Carcinoma of colon [RCV000009226] Chr11:48123636 [GRCh38]
Chr11:48145188 [GRCh37]
Chr11:11p11.2
pathogenic|other
NM_002843.4(PTPRJ):c.827A>C (p.Gln276Pro) single nucleotide variant Carcinoma of colon [RCV000009227]|not specified [RCV001777134] Chr11:48123823 [GRCh38]
Chr11:48145375 [GRCh37]
Chr11:11p11.2
pathogenic|benign|other
GRCh38/hg38 11p11.2(chr11:46840454-48643003)x1 copy number loss See cases [RCV000051014] Chr11:46840454..48643003 [GRCh38]
Chr11:46862005..48664555 [GRCh37]
Chr11:46818581..48621131 [NCBI36]
Chr11:11p11.2
pathogenic
GRCh38/hg38 11p11.2(chr11:47743903-48643003)x3 copy number gain See cases [RCV000051907] Chr11:47743903..48643003 [GRCh38]
Chr11:47765455..48664555 [GRCh37]
Chr11:47722031..48621131 [NCBI36]
Chr11:11p11.2
uncertain significance
GRCh38/hg38 11p12-11.2(chr11:36508280-48643003)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]|See cases [RCV000052680] Chr11:36508280..48643003 [GRCh38]
Chr11:36529830..48664555 [GRCh37]
Chr11:36486406..48621131 [NCBI36]
Chr11:11p12-11.2
pathogenic
NM_002843.3:c.3874+3G>T single nucleotide variant Malignant melanoma of skin [RCV000149742] Chr11:11p11.2 not provided
NM_002843.3:c.1258-1274delGTCATCCCCGGACTCCG deletion Malignant melanoma of skin [RCV000149743] Chr11:11p11.2 not provided
NM_002843.3(PTPRJ):c.2155C>T (p.Pro719Ser) single nucleotide variant Malignant melanoma of skin [RCV000149746] Chr11:48139488 [GRCh38]
Chr11:48161040 [GRCh37]
not provided
GRCh38/hg38 11p12-11.2(chr11:41118322-48643003)x1 copy number loss See cases [RCV000135405] Chr11:41118322..48643003 [GRCh38]
Chr11:41139872..48664555 [GRCh37]
Chr11:41096448..48621131 [NCBI36]
Chr11:11p12-11.2
pathogenic
GRCh38/hg38 11p12-11.12(chr11:39179252-49135735)x1 copy number loss See cases [RCV000137391] Chr11:39179252..49135735 [GRCh38]
Chr11:39200802..49157287 [GRCh37]
Chr11:39157378..49113863 [NCBI36]
Chr11:11p12-11.12
pathogenic
GRCh38/hg38 11p11.2(chr11:48067028-48761561)x3 copy number gain See cases [RCV000138155] Chr11:48067028..48761561 [GRCh38]
Chr11:48088580..48783113 [GRCh37]
Chr11:48045156..48739689 [NCBI36]
Chr11:11p11.2
conflicting data from submitters
GRCh38/hg38 11p11.2(chr11:47992987-48761561)x3 copy number gain See cases [RCV000137937] Chr11:47992987..48761561 [GRCh38]
Chr11:48014539..48783113 [GRCh37]
Chr11:47971115..48739689 [NCBI36]
Chr11:11p11.2
conflicting data from submitters
GRCh38/hg38 11p12-11.12(chr11:42727555-49135735)x3 copy number gain See cases [RCV000139422] Chr11:42727555..49135735 [GRCh38]
Chr11:42749105..49157287 [GRCh37]
Chr11:42705681..49113863 [NCBI36]
Chr11:11p12-11.12
likely pathogenic
GRCh38/hg38 11p11.2-11.12(chr11:47992987-49135735)x3 copy number gain See cases [RCV000139453] Chr11:47992987..49135735 [GRCh38]
Chr11:48014539..49157287 [GRCh37]
Chr11:47971115..49113863 [NCBI36]
Chr11:11p11.2-11.12
likely benign|uncertain significance
GRCh38/hg38 11p11.2(chr11:48110126-48623909)x3 copy number gain See cases [RCV000139996] Chr11:48110126..48623909 [GRCh38]
Chr11:48131678..48645461 [GRCh37]
Chr11:48088254..48602037 [NCBI36]
Chr11:11p11.2
likely benign
NM_002843.3(PTPRJ):c.1561C>A (p.Pro521Thr) single nucleotide variant Malignant melanoma of skin [RCV000149744] Chr11:48130662 [GRCh38]
Chr11:48152214 [GRCh37]
not provided
NM_002843.3(PTPRJ):c.1562C>T (p.Pro521Leu) single nucleotide variant Malignant melanoma of skin [RCV000149745] Chr11:48130663 [GRCh38]
Chr11:48152215 [GRCh37]
not provided
NM_002843.4(PTPRJ):c.1253G>A (p.Arg418His) single nucleotide variant not specified [RCV000194149] Chr11:48127939 [GRCh38]
Chr11:48149491 [GRCh37]
Chr11:11p11.2
likely benign
GRCh37/hg19 11p11.2-11.12(chr11:47711244-48976284)x3 copy number gain See cases [RCV000449235] Chr11:47711244..48976284 [GRCh37]
Chr11:11p11.2-11.12
uncertain significance
GRCh37/hg19 11p12-11.2(chr11:42475897-48372559)x1 copy number loss See cases [RCV000446383] Chr11:42475897..48372559 [GRCh37]
Chr11:11p12-11.2
pathogenic
GRCh37/hg19 11p11.2-11.12(chr11:48083277-48913631)x3 copy number gain See cases [RCV000446685] Chr11:48083277..48913631 [GRCh37]
Chr11:11p11.2-11.12
uncertain significance
GRCh37/hg19 11p11.2(chr11:48086949-48593349)x3 copy number gain See cases [RCV000448171] Chr11:48086949..48593349 [GRCh37]
Chr11:11p11.2
uncertain significance
GRCh37/hg19 11p11.2(chr11:48044621-48588884)x3 copy number gain See cases [RCV000448316] Chr11:48044621..48588884 [GRCh37]
Chr11:11p11.2
likely benign
GRCh37/hg19 11p14.2-11.12(chr11:26574629-50508019)x3 copy number gain See cases [RCV000448603] Chr11:26574629..50508019 [GRCh37]
Chr11:11p14.2-11.12
pathogenic
GRCh37/hg19 11p11.2-11.12(chr11:48095885-48913631)x3 copy number gain See cases [RCV000510398] Chr11:48095885..48913631 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p11.2-11.12(chr11:47748831-48985791)x3 copy number gain See cases [RCV000510265] Chr11:47748831..48985791 [GRCh37]
Chr11:11p11.2-11.12
uncertain significance
GRCh37/hg19 11p11.2(chr11:48007046-48721752)x3 copy number gain See cases [RCV000510600] Chr11:48007046..48721752 [GRCh37]
Chr11:11p11.2
uncertain significance
GRCh37/hg19 11p11.2-11.12(chr11:48116086-48913631)x3 copy number gain See cases [RCV000510344] Chr11:48116086..48913631 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p11.2-11.12(chr11:48086949-48925789)x3 copy number gain See cases [RCV000511498] Chr11:48086949..48925789 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p11.2-11.12(chr11:48149532-49434855)x3 copy number gain See cases [RCV000511753] Chr11:48149532..49434855 [GRCh37]
Chr11:11p11.2-11.12
uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p11.2-11.12(chr11:48087005-48925590)x3 copy number gain See cases [RCV000512518] Chr11:48087005..48925590 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p11.2(chr11:47773563-48403235)x3 copy number gain not provided [RCV000683344] Chr11:47773563..48403235 [GRCh37]
Chr11:11p11.2
uncertain significance
GRCh37/hg19 11p11.2-11.12(chr11:48065950-48893177)x3 copy number gain not provided [RCV000683350] Chr11:48065950..48893177 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p11.2-11.12(chr11:47720039-48891877)x3 copy number gain not provided [RCV000683356] Chr11:47720039..48891877 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p11.2-11.12(chr11:48116066-49170890)x3 copy number gain not provided [RCV000683353] Chr11:48116066..49170890 [GRCh37]
Chr11:11p11.2-11.12
likely benign
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p11.2(chr11:47760768-48518893)x3 copy number gain not provided [RCV000750031] Chr11:47760768..48518893 [GRCh37]
Chr11:11p11.2
benign
GRCh37/hg19 11p11.2(chr11:47825128-48601837)x3 copy number gain not provided [RCV000750032] Chr11:47825128..48601837 [GRCh37]
Chr11:11p11.2
benign
GRCh37/hg19 11p11.2(chr11:48068399-48558249)x3 copy number gain not provided [RCV000750033] Chr11:48068399..48558249 [GRCh37]
Chr11:11p11.2
benign
GRCh37/hg19 11p11.2-11.12(chr11:48068399-48878863)x3 copy number gain not provided [RCV000750034] Chr11:48068399..48878863 [GRCh37]
Chr11:11p11.2-11.12
benign
GRCh37/hg19 11p11.2(chr11:48146522-48588985)x0 copy number loss not provided [RCV000750035] Chr11:48146522..48588985 [GRCh37]
Chr11:11p11.2
benign
GRCh37/hg19 11p11.2(chr11:48190777-48388657)x0 copy number loss not provided [RCV000750036] Chr11:48190777..48388657 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.1352A>G (p.His451Arg) single nucleotide variant not provided [RCV000972485] Chr11:48128038 [GRCh38]
Chr11:48149590 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.877G>A (p.Ala293Thr) single nucleotide variant not provided [RCV000972121] Chr11:48124970 [GRCh38]
Chr11:48146522 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.3704T>C (p.Ile1235Thr) single nucleotide variant not provided [RCV000972122] Chr11:48163603 [GRCh38]
Chr11:48185155 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.100C>T (p.Leu34=) single nucleotide variant not provided [RCV000898727] Chr11:48110061 [GRCh38]
Chr11:48131613 [GRCh37]
Chr11:11p11.2
likely benign
NM_002843.4(PTPRJ):c.4008C>A (p.Ile1336=) single nucleotide variant not provided [RCV000954457] Chr11:48167356 [GRCh38]
Chr11:48188908 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.1411G>A (p.Gly471Ser) single nucleotide variant not provided [RCV000962139] Chr11:48130512 [GRCh38]
Chr11:48152064 [GRCh37]
Chr11:11p11.2
likely benign
NM_002843.4(PTPRJ):c.3042-6A>G single nucleotide variant not provided [RCV000892704] Chr11:48149984 [GRCh38]
Chr11:48171536 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.2444-7G>C single nucleotide variant not provided [RCV000908191] Chr11:48142912 [GRCh38]
Chr11:48164464 [GRCh37]
Chr11:11p11.2
likely benign
NM_002843.4(PTPRJ):c.1905T>A (p.Ser635Arg) single nucleotide variant not provided [RCV000891469] Chr11:48137034 [GRCh38]
Chr11:48158586 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.575A>G (p.Asn192Ser) single nucleotide variant not provided [RCV000956939] Chr11:48121225 [GRCh38]
Chr11:48142777 [GRCh37]
Chr11:11p11.2
benign
NM_002843.4(PTPRJ):c.2876G>A (p.Arg959His) single nucleotide variant not provided [RCV001579681] Chr11:48145089 [GRCh38]
Chr11:48166641 [GRCh37]
Chr11:11p11.2
likely benign
GRCh37/hg19 11p11.2(chr11:47997461-48142707)x3 copy number gain Aortic valve stenosis [RCV001250257] Chr11:47997461..48142707 [GRCh37]
Chr11:11p11.2
uncertain significance
GRCh37/hg19 11p11.2(chr11:47852329-48010053)x1 copy number loss not provided [RCV001006410] Chr11:47852329..48010053 [GRCh37]
Chr11:11p11.2
uncertain significance
NM_002843.4(PTPRJ):c.3373C>T (p.Arg1125Cys) single nucleotide variant not provided [RCV001355541] Chr11:48156054 [GRCh38]
Chr11:48177606 [GRCh37]
Chr11:11p11.2
uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9673 AgrOrtholog
COSMIC PTPRJ COSMIC
Ensembl Genes ENSG00000149177 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000400010 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000409733 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000432686 UniProtKB/TrEMBL
  ENSP00000435618 UniProtKB/TrEMBL
  ENSP00000477933 UniProtKB/TrEMBL
  ENSP00000479342 UniProtKB/TrEMBL
Ensembl Transcript ENST00000418331 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000440289 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000527952 UniProtKB/TrEMBL
  ENST00000534219 UniProtKB/TrEMBL
  ENST00000613246 UniProtKB/TrEMBL
  ENST00000615445 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.90.190.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000149177 GTEx
HGNC ID HGNC:9673 ENTREZGENE
Human Proteome Map PTPRJ Human Proteome Map
InterPro FN3_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FN3_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot-tyrosine_phosphatase-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTPase_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTPRJ_TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tyr_Pase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tyr_Pase_cat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TYR_PHOSPHATASE_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5795 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 5795 ENTREZGENE
OMIM 114500 OMIM
  600925 OMIM
Pfam fn3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTP_tm UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Y_phosphatase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34018 PharmGKB
PRINTS PRTYPHPHTASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE FN3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TYR_PHOSPHATASE_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TYR_PHOSPHATASE_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TYR_PHOSPHATASE_PTP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART FN3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTPc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTPc_motif UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49265 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52799 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTK0_HUMAN UniProtKB/TrEMBL
  A0A087WVC6_HUMAN UniProtKB/TrEMBL
  E9PJ83_HUMAN UniProtKB/TrEMBL
  E9PPH3_HUMAN UniProtKB/TrEMBL
  PTPRJ_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q9NPR5 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary E9PG76 UniProtKB/TrEMBL
  Q15255 UniProtKB/Swiss-Prot
  Q6P4H4 UniProtKB/Swiss-Prot
  Q8NHM2 UniProtKB/Swiss-Prot
  Q9UDA9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-02-19 PTPRJ  protein tyrosine phosphatase receptor type J    protein tyrosine phosphatase, receptor type J  Symbol and/or name change 5135510 APPROVED
2016-01-12 PTPRJ  protein tyrosine phosphatase, receptor type J    protein tyrosine phosphatase, receptor type, J  Symbol and/or name change 5135510 APPROVED
2011-08-16 PTPRJ  protein tyrosine phosphatase, receptor type, J  PTPRJ  protein tyrosine phosphatase, receptor type, J  Symbol and/or name change 5135510 APPROVED