PTPRZ1 (protein tyrosine phosphatase receptor type Z1) - Rat Genome Database

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Gene: PTPRZ1 (protein tyrosine phosphatase receptor type Z1) Homo sapiens
Analyze
Symbol: PTPRZ1
Name: protein tyrosine phosphatase receptor type Z1
RGD ID: 731607
HGNC Page HGNC
Description: Exhibits integrin binding activity and protein tyrosine phosphatase activity. Predicted to be involved in several processes, including oligodendrocyte differentiation; peptidyl-tyrosine dephosphorylation; and regulation of nervous system development. Localizes to plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: HPTPZ; HPTPzeta; phosphacan; protein tyrosine phosphatase, receptor-type, zeta polypeptide 1; protein-tyrosine phosphatase receptor type Z polypeptide 1; protein-tyrosine phosphatase receptor type Z polypeptide 2; PTP-ZETA; PTP18; PTPRZ; PTPZ; R-PTP-zeta; R-PTP-zeta-2; receptor-type tyrosine phosphatase beta/zeta; receptor-type tyrosine-protein phosphatase zeta; RPTPB; RPTPbeta
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 Ensembl7121,873,089 - 122,062,036 (+)EnsemblGRCh38hg38GRCh38
GRCh387121,873,161 - 122,062,036 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377121,513,215 - 121,702,090 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367121,300,395 - 121,489,326 (+)NCBINCBI36hg18NCBI36
Build 347121,107,357 - 121,296,039NCBI
Celera7116,322,385 - 116,511,311 (+)NCBI
Cytogenetic Map7q31.32NCBI
HuRef7115,876,018 - 116,065,533 (+)NCBIHuRef
CHM1_17121,446,481 - 121,635,390 (+)NCBICHM1_1
CRA_TCAGchr7v27120,907,807 - 121,096,757 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-pilocarpine  (ISO)
(+)-schisandrin B  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-hydroxypropanoic acid  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,4-dichloroaniline  (EXP)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acetaldehyde  (ISO)
acetamide  (ISO)
acrylamide  (EXP,ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (ISO)
bisphenol F  (ISO)
cadmium dichloride  (ISO)
calcitriol  (EXP)
carbamazepine  (EXP,ISO)
carbon nanotube  (ISO)
chrysene  (ISO)
ciguatoxin CTX1B  (ISO)
cisplatin  (ISO)
cobalt atom  (EXP)
cobalt dichloride  (EXP)
cyclosporin A  (ISO)
cytarabine  (EXP)
dimethylarsinous acid  (EXP)
diuron  (EXP)
dorsomorphin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
fenvalerate  (ISO)
flutamide  (ISO)
furan  (ISO)
genistein  (ISO)
iron(III) nitrilotriacetate  (ISO)
lead(0)  (EXP)
lead(2+)  (EXP)
manganese(II) chloride  (ISO)
methyl beta-cyclodextrin  (EXP)
methylmercury chloride  (EXP)
miconazole  (ISO)
oxaliplatin  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (EXP,ISO)
rac-lactic acid  (EXP)
SB 431542  (EXP)
sodium arsenite  (EXP)
sodium dodecyl sulfate  (EXP)
tacrolimus hydrate  (ISO)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
triclosan  (EXP)
Tungsten carbide  (EXP)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:1323835   PMID:2169617   PMID:2170109   PMID:7736789   PMID:8387522   PMID:9441757   PMID:9507007   PMID:9653645   PMID:9847074   PMID:10212223   PMID:10521598   PMID:10706604  
PMID:11381105   PMID:11520897   PMID:11707406   PMID:12355066   PMID:12477932   PMID:12690205   PMID:12700241   PMID:14555979   PMID:15523497   PMID:15797857   PMID:15833863   PMID:15908427  
PMID:15925565   PMID:15998549   PMID:16105548   PMID:16335952   PMID:16338072   PMID:16344560   PMID:16513268   PMID:16814777   PMID:17030583   PMID:17098867   PMID:17368428   PMID:17579610  
PMID:17681947   PMID:17706593   PMID:17727841   PMID:17823238   PMID:18003890   PMID:18186075   PMID:18713734   PMID:18838383   PMID:19058221   PMID:19141530   PMID:19167335   PMID:19604403  
PMID:20133774   PMID:20201926   PMID:20224786   PMID:20738847   PMID:21454675   PMID:21873635   PMID:21890632   PMID:21969550   PMID:21976490   PMID:22682003   PMID:22832403   PMID:23060448  
PMID:23100427   PMID:23161541   PMID:23170925   PMID:23226095   PMID:23570448   PMID:23588815   PMID:23744080   PMID:23777859   PMID:24242166   PMID:25135958   PMID:25238264   PMID:25644401  
PMID:25935522   PMID:26186194   PMID:26851024   PMID:27445335   PMID:28319085   PMID:28504721   PMID:28514442   PMID:28569747   PMID:28717188   PMID:29651006   PMID:29791485   PMID:29987050  
PMID:30497491   PMID:31364003   PMID:31381204  


Genomics

Comparative Map Data
PTPRZ1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7121,873,089 - 122,062,036 (+)EnsemblGRCh38hg38GRCh38
GRCh387121,873,161 - 122,062,036 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377121,513,215 - 121,702,090 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367121,300,395 - 121,489,326 (+)NCBINCBI36hg18NCBI36
Build 347121,107,357 - 121,296,039NCBI
Celera7116,322,385 - 116,511,311 (+)NCBI
Cytogenetic Map7q31.32NCBI
HuRef7115,876,018 - 116,065,533 (+)NCBIHuRef
CHM1_17121,446,481 - 121,635,390 (+)NCBICHM1_1
CRA_TCAGchr7v27120,907,807 - 121,096,757 (+)NCBI
Ptprz1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39622,875,302 - 23,052,915 (+)NCBIGRCm39mm39
GRCm39 Ensembl622,875,501 - 23,052,915 (+)Ensembl
GRCm38622,875,315 - 23,052,916 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl622,875,502 - 23,052,916 (+)EnsemblGRCm38mm10GRCm38
MGSCv37622,825,502 - 23,002,916 (+)NCBIGRCm37mm9NCBIm37
MGSCv36622,825,503 - 23,002,917 (+)NCBImm8
Celera622,923,288 - 23,100,277 (+)NCBICelera
Cytogenetic Map6A3.1NCBI
Ptprz1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2451,397,316 - 51,595,220 (+)NCBI
Rnor_6.0 Ensembl449,941,304 - 50,140,762 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0449,941,046 - 50,140,764 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0449,730,302 - 49,927,328 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4449,267,521 - 49,468,692 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1449,498,094 - 49,699,266 (+)NCBI
Celera446,598,237 - 46,787,500 (+)NCBICelera
Cytogenetic Map4q22NCBI
Ptprz1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554793,624,993 - 3,733,183 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554793,611,658 - 3,734,225 (+)NCBIChiLan1.0ChiLan1.0
PTPRZ1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.17126,569,630 - 126,758,155 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7126,569,630 - 126,758,155 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v07113,882,557 - 114,073,283 (+)NCBIMhudiblu_PPA_v0panPan3
PTPRZ1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11459,769,553 - 59,944,111 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1459,827,650 - 59,943,315 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1459,203,408 - 59,361,617 (+)NCBI
ROS_Cfam_1.01459,825,102 - 59,979,392 (+)NCBI
UMICH_Zoey_3.11459,916,795 - 60,071,051 (+)NCBI
UNSW_CanFamBas_1.01459,543,462 - 59,698,673 (+)NCBI
UU_Cfam_GSD_1.01459,919,950 - 60,076,006 (+)NCBI
Ptprz1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511848,835,842 - 49,007,255 (+)NCBI
SpeTri2.0NW_0049366053,195,893 - 3,368,102 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PTPRZ1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1825,045,727 - 25,228,247 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11825,046,027 - 25,228,276 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21826,650,579 - 26,832,837 (-)NCBISscrofa10.2Sscrofa10.2susScr3
PTPRZ1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12190,686,091 - 90,877,538 (+)NCBI
ChlSab1.1 Ensembl2190,686,167 - 90,877,649 (+)Ensembl
Ptprz1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462478313,911,525 - 14,105,403 (-)NCBI

Position Markers
SHGC-36248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,550,519 - 121,550,629UniSTSGRCh37
Build 367121,337,755 - 121,337,865RGDNCBI36
Celera7116,359,732 - 116,359,842RGD
Cytogenetic Map7q31.3UniSTS
HuRef7115,913,427 - 115,913,537UniSTS
CRA_TCAGchr7v27120,945,183 - 120,945,293UniSTS
TNG Radiation Hybrid Map754584.0UniSTS
Stanford-G3 RH Map75961.0UniSTS
NCBI RH Map7995.0UniSTS
GeneMap99-G3 RH Map75961.0UniSTS
D7S466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,680,656 - 121,680,906UniSTSGRCh37
Build 367121,467,892 - 121,468,142RGDNCBI36
Celera7116,489,877 - 116,490,121RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,043,708 - 116,043,956UniSTS
CRA_TCAGchr7v27121,075,323 - 121,075,567UniSTS
D7S2737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,701,356 - 121,701,461UniSTSGRCh37
Build 367121,488,592 - 121,488,697RGDNCBI36
Celera7116,510,577 - 116,510,682RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,064,799 - 116,064,904UniSTS
CRA_TCAGchr7v27121,096,023 - 121,096,128UniSTS
Stanford-G3 RH Map75928.0UniSTS
NCBI RH Map71114.5UniSTS
GeneMap99-G3 RH Map75928.0UniSTS
RH26920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,652,778 - 121,652,870UniSTSGRCh37
Build 367121,440,014 - 121,440,106RGDNCBI36
Celera7116,461,991 - 116,462,083RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,015,793 - 116,015,885UniSTS
CRA_TCAGchr7v27121,047,438 - 121,047,530UniSTS
RH122873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,544,899 - 121,545,238UniSTSGRCh37
Build 367121,332,135 - 121,332,474RGDNCBI36
Celera7116,354,112 - 116,354,451RGD
Cytogenetic Map7q31.3UniSTS
HuRef7115,907,786 - 115,908,125UniSTS
CRA_TCAGchr7v27120,939,563 - 120,939,902UniSTS
TNG Radiation Hybrid Map754577.0UniSTS
RH122881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,676,383 - 121,676,709UniSTSGRCh37
Build 367121,463,619 - 121,463,945RGDNCBI36
Celera7116,485,606 - 116,485,932RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,039,437 - 116,039,763UniSTS
CRA_TCAGchr7v27121,071,052 - 121,071,378UniSTS
TNG Radiation Hybrid Map754604.0UniSTS
RH47696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,678,820 - 121,678,944UniSTSGRCh37
Build 367121,466,056 - 121,466,180RGDNCBI36
Celera7116,488,041 - 116,488,165RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,041,872 - 116,041,996UniSTS
CRA_TCAGchr7v27121,073,487 - 121,073,611UniSTS
GeneMap99-GB4 RH Map7564.16UniSTS
NCBI RH Map71123.7UniSTS
PTPRZ1_2426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,701,386 - 121,702,274UniSTSGRCh37
Build 367121,488,622 - 121,489,510RGDNCBI36
Celera7116,510,607 - 116,511,495RGD
HuRef7116,064,829 - 116,065,717UniSTS
CRA_TCAGchr7v27121,096,053 - 121,096,941UniSTS
D7S601E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,652,931 - 121,653,032UniSTSGRCh37
Build 367121,440,167 - 121,440,268RGDNCBI36
Celera7116,462,144 - 116,462,245RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,015,946 - 116,016,047UniSTS
CRA_TCAGchr7v27121,047,591 - 121,047,692UniSTS
PTPRZ  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,701,887 - 121,702,038UniSTSGRCh37
Build 367121,489,123 - 121,489,274RGDNCBI36
Celera7116,511,108 - 116,511,259RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,065,330 - 116,065,481UniSTS
CRA_TCAGchr7v27121,096,554 - 121,096,705UniSTS
SHGC-30278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377121,701,931 - 121,702,064UniSTSGRCh37
Build 367121,489,167 - 121,489,300RGDNCBI36
Celera7116,511,152 - 116,511,285RGD
Cytogenetic Map7q31.3UniSTS
HuRef7116,065,374 - 116,065,507UniSTS
CRA_TCAGchr7v27121,096,598 - 121,096,731UniSTS
TNG Radiation Hybrid Map754612.0UniSTS
GeneMap99-GB4 RH Map7564.16UniSTS
Whitehead-RH Map7509.6UniSTS
GeneMap99-G3 RH Map75928.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:921
Count of miRNA genes:620
Interacting mature miRNAs:689
Transcripts:ENST00000393386, ENST00000449182, ENST00000468641, ENST00000470504, ENST00000471837, ENST00000474500, ENST00000483028, ENST00000483995, ENST00000489114
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
High 9 1
Medium 223 19 27 5 15 3 1437 26 2805 8 35 91 3 24 718
Low 1832 1404 491 176 258 16 1316 922 850 50 823 724 167 569 985
Below cutoff 258 1386 1041 319 835 322 1573 1186 25 171 459 683 3 1 611 1059 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_023266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC073095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC131736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX868991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX872418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA101746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA454064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M93426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U88967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X54135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000393386   ⟹   ENSP00000377047
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,161 - 122,062,036 (+)Ensembl
RefSeq Acc Id: ENST00000449182   ⟹   ENSP00000410000
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,361 - 122,061,361 (+)Ensembl
RefSeq Acc Id: ENST00000468641
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,033,858 - 122,036,632 (+)Ensembl
RefSeq Acc Id: ENST00000470504
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,034,013 - 122,039,584 (+)Ensembl
RefSeq Acc Id: ENST00000471837
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,161 - 121,967,023 (+)Ensembl
RefSeq Acc Id: ENST00000474500
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,059,374 - 122,061,692 (+)Ensembl
RefSeq Acc Id: ENST00000483028
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,011,208 - 122,013,312 (+)Ensembl
RefSeq Acc Id: ENST00000483995
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,028,434 - 122,032,080 (+)Ensembl
RefSeq Acc Id: ENST00000489114
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,028,218 - 122,034,340 (+)Ensembl
RefSeq Acc Id: ENST00000650681   ⟹   ENSP00000498708
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,182 - 122,061,871 (+)Ensembl
RefSeq Acc Id: ENST00000650728   ⟹   ENSP00000499152
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,161 - 122,061,637 (+)Ensembl
RefSeq Acc Id: ENST00000650826   ⟹   ENSP00000498356
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,152 - 122,061,877 (+)Ensembl
RefSeq Acc Id: ENST00000651065   ⟹   ENSP00000499073
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,089 - 122,061,957 (+)Ensembl
RefSeq Acc Id: ENST00000651320   ⟹   ENSP00000498388
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,481 - 122,061,979 (+)Ensembl
RefSeq Acc Id: ENST00000651390   ⟹   ENSP00000498965
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,166 - 122,061,828 (+)Ensembl
RefSeq Acc Id: ENST00000651841   ⟹   ENSP00000499061
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,013,706 - 122,061,840 (+)Ensembl
RefSeq Acc Id: ENST00000651842   ⟹   ENSP00000499098
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,166 - 122,061,828 (+)Ensembl
RefSeq Acc Id: ENST00000651863   ⟹   ENSP00000498439
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,327 - 122,061,822 (+)Ensembl
RefSeq Acc Id: ENST00000652054   ⟹   ENSP00000498722
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,161 - 122,061,669 (+)Ensembl
RefSeq Acc Id: ENST00000652298   ⟹   ENSP00000499137
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7121,873,357 - 122,062,016 (+)Ensembl
RefSeq Acc Id: ENST00000652708   ⟹   ENSP00000499039
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7122,013,313 - 122,061,994 (+)Ensembl
RefSeq Acc Id: NM_001206838   ⟹   NP_001193767
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 122,062,036 (+)NCBI
GRCh377121,513,159 - 121,702,090 (+)ENTREZGENE
HuRef7115,876,018 - 116,065,533 (+)ENTREZGENE
CHM1_17121,446,481 - 121,635,390 (+)NCBI
CRA_TCAGchr7v27120,907,807 - 121,096,757 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001206839   ⟹   NP_001193768
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 122,062,036 (+)NCBI
GRCh377121,513,159 - 121,702,090 (+)ENTREZGENE
HuRef7115,876,018 - 116,065,533 (+)ENTREZGENE
CHM1_17121,446,481 - 121,635,390 (+)NCBI
CRA_TCAGchr7v27120,907,807 - 121,096,757 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001369395   ⟹   NP_001356324
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 122,062,036 (+)NCBI
RefSeq Acc Id: NM_001369396   ⟹   NP_001356325
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 122,062,036 (+)NCBI
RefSeq Acc Id: NM_002851   ⟹   NP_002842
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 122,062,036 (+)NCBI
GRCh377121,513,159 - 121,702,090 (+)ENTREZGENE
GRCh377121,513,159 - 121,702,090 (+)NCBI
Build 367121,300,395 - 121,489,326 (+)NCBI Archive
HuRef7115,876,018 - 116,065,533 (+)ENTREZGENE
CHM1_17121,446,481 - 121,635,390 (+)NCBI
CRA_TCAGchr7v27120,907,807 - 121,096,757 (+)ENTREZGENE
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002842   ⟸   NM_002851
- Peptide Label: isoform 1 precursor
- UniProtKB: P23471 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001193767   ⟸   NM_001206838
- Peptide Label: isoform 2 precursor
- UniProtKB: P23471 (UniProtKB/Swiss-Prot),   B4DFE7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001193768   ⟸   NM_001206839
- Peptide Label: isoform 3 precursor
- UniProtKB: P23471 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001356325   ⟸   NM_001369396
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001356324   ⟸   NM_001369395
- Peptide Label: isoform 4 precursor
RefSeq Acc Id: ENSP00000498356   ⟸   ENST00000650826
RefSeq Acc Id: ENSP00000499152   ⟸   ENST00000650728
RefSeq Acc Id: ENSP00000498708   ⟸   ENST00000650681
RefSeq Acc Id: ENSP00000498439   ⟸   ENST00000651863
RefSeq Acc Id: ENSP00000499098   ⟸   ENST00000651842
RefSeq Acc Id: ENSP00000499061   ⟸   ENST00000651841
RefSeq Acc Id: ENSP00000498388   ⟸   ENST00000651320
RefSeq Acc Id: ENSP00000498965   ⟸   ENST00000651390
RefSeq Acc Id: ENSP00000499073   ⟸   ENST00000651065
RefSeq Acc Id: ENSP00000499137   ⟸   ENST00000652298
RefSeq Acc Id: ENSP00000498722   ⟸   ENST00000652054
RefSeq Acc Id: ENSP00000499039   ⟸   ENST00000652708
RefSeq Acc Id: ENSP00000377047   ⟸   ENST00000393386
RefSeq Acc Id: ENSP00000410000   ⟸   ENST00000449182
Promoters
RGD ID:7211803
Promoter ID:EPDNEW_H11647
Type:initiation region
Name:PTPRZ1_1
Description:protein tyrosine phosphatase, receptor type Z1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387121,873,161 - 121,873,221EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q31.1-31.33(chr7:113799835-124899218)x1 copy number loss See cases [RCV000054160] Chr7:113799835..124899218 [GRCh38]
Chr7:113439890..124539272 [GRCh37]
Chr7:113227126..124326508 [NCBI36]
Chr7:7q31.1-31.33
pathogenic
NM_002851.2(PTPRZ1):c.266C>T (p.Ser89Leu) single nucleotide variant Malignant melanoma [RCV000067603] Chr7:121968092 [GRCh38]
Chr7:121608146 [GRCh37]
Chr7:121395382 [NCBI36]
Chr7:7q31.32
not provided
NM_002851.2(PTPRZ1):c.4535C>T (p.Ser1512Phe) single nucleotide variant Malignant melanoma [RCV000061545] Chr7:122013581 [GRCh38]
Chr7:121653635 [GRCh37]
Chr7:121440871 [NCBI36]
Chr7:7q31.32
not provided
NM_002851.3(PTPRZ1):c.663G>T (p.Leu221=) single nucleotide variant not provided [RCV000087204] Chr7:121983708 [GRCh38]
Chr7:121623762 [GRCh37]
Chr7:7q31.32
uncertain significance
GRCh38/hg38 7q31.1-31.33(chr7:114142477-125840381)x1 copy number loss See cases [RCV000135311] Chr7:114142477..125840381 [GRCh38]
Chr7:113782532..125480435 [GRCh37]
Chr7:113569768..125267671 [NCBI36]
Chr7:7q31.1-31.33
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q31.32(chr7:121461314-122882795)x1 copy number loss See cases [RCV000137140] Chr7:121461314..122882795 [GRCh38]
Chr7:121101368..122522849 [GRCh37]
Chr7:120888604..122310085 [NCBI36]
Chr7:7q31.32
uncertain significance
GRCh38/hg38 7q31.2-33(chr7:117326805-134790689)x1 copy number loss See cases [RCV000138226] Chr7:117326805..134790689 [GRCh38]
Chr7:116966859..134475440 [GRCh37]
Chr7:116754095..134125980 [NCBI36]
Chr7:7q31.2-33
pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3
pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3
pathogenic
GRCh38/hg38 7q31.32-32.1(chr7:122018122-128907727)x1 copy number loss See cases [RCV000142521] Chr7:122018122..128907727 [GRCh38]
Chr7:121658176..128547780 [GRCh37]
Chr7:121445412..128335016 [NCBI36]
Chr7:7q31.32-32.1
pathogenic
GRCh37/hg19 7q31.1-32.1(chr7:111613396-127897316)x1 copy number loss See cases [RCV000240177] Chr7:111613396..127897316 [GRCh37]
Chr7:7q31.1-32.1
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_002851.3(PTPRZ1):c.552+9T>C single nucleotide variant not provided [RCV000900624] Chr7:121976277 [GRCh38]
Chr7:121616331 [GRCh37]
Chr7:7q31.32
likely benign
NM_002851.3(PTPRZ1):c.3864T>C (p.Ser1288=) single nucleotide variant not provided [RCV000968886] Chr7:122012910 [GRCh38]
Chr7:121652964 [GRCh37]
Chr7:7q31.32
benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_002851.3(PTPRZ1):c.6169A>G (p.Ile2057Val) single nucleotide variant Severe Myopia [RCV000785673] Chr7:122051512 [GRCh38]
Chr7:121691566 [GRCh37]
Chr7:7q31.32
uncertain significance
NM_002851.3(PTPRZ1):c.4899C>T (p.Ser1633=) single nucleotide variant not provided [RCV000923227] Chr7:122019179 [GRCh38]
Chr7:121659233 [GRCh37]
Chr7:7q31.32
likely benign
NM_002851.3(PTPRZ1):c.879T>C (p.Ser293=) single nucleotide variant not provided [RCV000917504] Chr7:121984068 [GRCh38]
Chr7:121624122 [GRCh37]
Chr7:7q31.32
benign
GRCh37/hg19 7q31.32(chr7:121467966-121532823)x3 copy number gain not provided [RCV000847152] Chr7:121467966..121532823 [GRCh37]
Chr7:7q31.32
uncertain significance
GRCh37/hg19 7q31.32-32.2(chr7:121480906-129389003)x1 copy number loss not provided [RCV000847911] Chr7:121480906..129389003 [GRCh37]
Chr7:7q31.32-32.2
pathogenic
GRCh37/hg19 7q22.3-31.32(chr7:106617406-123217914)x1 copy number loss not provided [RCV001005991] Chr7:106617406..123217914 [GRCh37]
Chr7:7q22.3-31.32
pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3
pathogenic
GRCh37/hg19 7q31.32(chr7:121467966-121532823)x3 copy number gain not provided [RCV000846737] Chr7:121467966..121532823 [GRCh37]
Chr7:7q31.32
uncertain significance
NM_002851.3(PTPRZ1):c.5081-4G>A single nucleotide variant not provided [RCV000914896] Chr7:122031470 [GRCh38]
Chr7:121671524 [GRCh37]
Chr7:7q31.32
benign
NM_002851.3(PTPRZ1):c.3070G>C (p.Val1024Leu) single nucleotide variant not provided [RCV000953254] Chr7:122012116 [GRCh38]
Chr7:121652170 [GRCh37]
Chr7:7q31.32
benign
NM_002851.3(PTPRZ1):c.3238A>C (p.Lys1080Gln) single nucleotide variant not provided [RCV000953255] Chr7:122012284 [GRCh38]
Chr7:121652338 [GRCh37]
Chr7:7q31.32
benign
NM_002851.3(PTPRZ1):c.1098T>C (p.Asp366=) single nucleotide variant not provided [RCV000904226] Chr7:121996551 [GRCh38]
Chr7:121636605 [GRCh37]
Chr7:7q31.32
likely benign
NM_002851.3(PTPRZ1):c.3498G>A (p.Gln1166=) single nucleotide variant not provided [RCV000954039] Chr7:122012544 [GRCh38]
Chr7:121652598 [GRCh37]
Chr7:7q31.32
benign
NM_002851.3(PTPRZ1):c.2121T>C (p.Asp707=) single nucleotide variant not provided [RCV000890712] Chr7:122011167 [GRCh38]
Chr7:121651221 [GRCh37]
Chr7:7q31.32
benign
NC_000007.14:g.122004613_122004618del deletion Spastic paraparesis [RCV001253051] Chr7:122004613..122004618 [GRCh38]
Chr7:121644667..121644672 [GRCh37]
Chr7:7q31.32
uncertain significance
GRCh37/hg19 7q31.2-31.33(chr7:116297277-126370694) copy number loss Global developmental delay [RCV001352642] Chr7:116297277..126370694 [GRCh37]
Chr7:7q31.2-31.33
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9685 AgrOrtholog
COSMIC PTPRZ1 COSMIC
Ensembl Genes ENSG00000106278 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000377047 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000410000 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000498356 UniProtKB/TrEMBL
  ENSP00000498388 UniProtKB/TrEMBL
  ENSP00000498439 UniProtKB/TrEMBL
  ENSP00000498708 UniProtKB/TrEMBL
  ENSP00000498722 UniProtKB/TrEMBL
  ENSP00000498965 UniProtKB/TrEMBL
  ENSP00000499039 UniProtKB/TrEMBL
  ENSP00000499061 UniProtKB/TrEMBL
  ENSP00000499073 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000499098 UniProtKB/TrEMBL
  ENSP00000499137 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000499152 UniProtKB/TrEMBL
Ensembl Transcript ENST00000393386 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000449182 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000650681 UniProtKB/TrEMBL
  ENST00000650728 UniProtKB/TrEMBL
  ENST00000650826 UniProtKB/TrEMBL
  ENST00000651065 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000651320 UniProtKB/TrEMBL
  ENST00000651390 UniProtKB/TrEMBL
  ENST00000651841 UniProtKB/TrEMBL
  ENST00000651842 UniProtKB/TrEMBL
  ENST00000651863 UniProtKB/TrEMBL
  ENST00000652054 UniProtKB/TrEMBL
  ENST00000652298 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000652708 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.10.200.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.90.190.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000106278 GTEx
HGNC ID HGNC:9685 ENTREZGENE
Human Proteome Map PTPRZ1 Human Proteome Map
InterPro alpha_CARP_receptor-type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CA_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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
  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:5803 UniProtKB/Swiss-Prot
NCBI Gene 5803 ENTREZGENE
OMIM 176891 OMIM
Pfam Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  fn3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Y_phosphatase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34029 PharmGKB
PRINTS PRTYPHPHTASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ALPHA_CA_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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 Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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
  SSF51069 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52799 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A494C036_HUMAN UniProtKB/TrEMBL
  A0A494C055_HUMAN UniProtKB/TrEMBL
  A0A494C087_HUMAN UniProtKB/TrEMBL
  A0A494C0U4_HUMAN UniProtKB/TrEMBL
  A0A494C0V2_HUMAN UniProtKB/TrEMBL
  A0A494C1B4_HUMAN UniProtKB/TrEMBL
  A0A494C1F0_HUMAN UniProtKB/TrEMBL
  A0A494C1H9_HUMAN UniProtKB/TrEMBL
  A0A494C1J5_HUMAN UniProtKB/TrEMBL
  A0A494C1R4_HUMAN UniProtKB/TrEMBL
  B4DFE7 ENTREZGENE, UniProtKB/TrEMBL
  P23471 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A4D0W5 UniProtKB/Swiss-Prot
  C9JFM0 UniProtKB/Swiss-Prot
  O76043 UniProtKB/Swiss-Prot
  Q9UDR6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-02-19 PTPRZ1  protein tyrosine phosphatase receptor type Z1  PTPRZ1  protein tyrosine phosphatase, receptor type Z1  Symbol and/or name change 5135510 APPROVED
2016-01-12 PTPRZ1  protein tyrosine phosphatase, receptor type Z1  PTPRZ1  protein tyrosine phosphatase, receptor-type, Z polypeptide 1  Symbol and/or name change 5135510 APPROVED