PTPRG (protein tyrosine phosphatase receptor type G) - Rat Genome Database

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Gene: PTPRG (protein tyrosine phosphatase receptor type G) Homo sapiens
Analyze
Symbol: PTPRG
Name: protein tyrosine phosphatase receptor type G
RGD ID: 735532
HGNC Page HGNC
Description: Exhibits identical protein binding activity and protein tyrosine phosphatase activity. Involved in negative regulation of epithelial cell migration. Localizes to extracellular exosome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: H_RG317H01.1; HPTPG; protein tyrosine phosphatase gamma; protein tyrosine phosphatase, receptor type, gamma polypeptide; protein-tyrosine phosphatase gamma; PTPG; R-PTP-GAMMA; receptor type protein tyrosine phosphatase gamma; receptor tyrosine phosphatase gamma; receptor-type protein phosphatase gamma; receptor-type tyrosine-protein phosphatase gamma; RPTPG
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 Ensembl361,561,569 - 62,297,609 (+)EnsemblGRCh38hg38GRCh38
GRCh38361,561,571 - 62,297,609 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37361,547,245 - 62,283,284 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36361,522,285 - 62,254,738 (+)NCBINCBI36hg18NCBI36
Build 34361,522,284 - 62,254,737NCBI
Celera361,560,149 - 62,297,663 (+)NCBI
Cytogenetic Map3p14.2NCBI
HuRef361,645,865 - 62,378,614 (+)NCBIHuRef
CHM1_1361,497,665 - 62,231,710 (+)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
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4-hydroxyphenyl retinamide  (ISO)
4-tert-Octylphenol  (ISO)
4-vinylcyclohexene dioxide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
7,12-dimethyltetraphene  (ISO)
acetamide  (ISO)
afimoxifene  (EXP)
aflatoxin B1  (EXP,ISO)
aflatoxin B2  (EXP)
all-trans-retinoic acid  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bis(2-chloroethyl) sulfide  (ISO)
bisphenol A  (ISO)
bromobenzene  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
carbon nanotube  (ISO)
chlordecone  (ISO)
chrysene  (ISO)
cisplatin  (EXP,ISO)
clofibrate  (ISO)
cobalt dichloride  (EXP)
copper atom  (ISO)
copper(0)  (ISO)
cyclosporin A  (EXP)
dexamethasone  (EXP)
dibenz[a,h]anthracene  (ISO)
diethylstilbestrol  (ISO)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
flutamide  (ISO)
folic acid  (ISO)
fonofos  (EXP)
fulvestrant  (EXP)
genistein  (ISO)
irinotecan  (EXP)
isotretinoin  (EXP)
lead(0)  (EXP)
lead(2+)  (EXP)
leflunomide  (EXP,ISO)
melphalan  (EXP)
methapyrilene  (ISO)
methotrexate  (EXP)
methoxychlor  (ISO)
methylmercury chloride  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (EXP)
N-nitrosomorpholine  (ISO)
nickel sulfate  (EXP)
p-tert-Amylphenol  (ISO)
paracetamol  (ISO)
parathion  (EXP)
phenobarbital  (ISO)
potassium chromate  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
sodium arsenite  (EXP)
sodium dichromate  (ISO)
sodium fluoride  (ISO)
sulforaphane  (ISO)
sunitinib  (EXP)
terbufos  (EXP)
Tesaglitazar  (ISO)
tetraphene  (ISO)
troglitazone  (ISO)
valproic acid  (EXP)
vinclozolin  (ISO)
zoledronic acid  (EXP)

References

Additional References at PubMed
PMID:1711217   PMID:2169617   PMID:2170109   PMID:7683956   PMID:8382771   PMID:8833149   PMID:10376795   PMID:10521598   PMID:11859871   PMID:12477932   PMID:12553013   PMID:14676845  
PMID:15897551   PMID:15978577   PMID:16335952   PMID:17963294   PMID:18646686   PMID:18829573   PMID:19167335   PMID:19567891   PMID:20031603   PMID:20125088   PMID:20133774   PMID:20201926  
PMID:20379614   PMID:20651337   PMID:20825314   PMID:20959494   PMID:21112398   PMID:21126580   PMID:21150880   PMID:21724833   PMID:21795790   PMID:21873635   PMID:21926974   PMID:22747683  
PMID:23319000   PMID:23376485   PMID:23532252   PMID:23533145   PMID:23758498   PMID:24496747   PMID:25158255   PMID:25196286   PMID:25299301   PMID:25624455   PMID:25775014   PMID:25970784  
PMID:26186194   PMID:26830138   PMID:27173435   PMID:27602768   PMID:27880917   PMID:28514442   PMID:28611215   PMID:28637510   PMID:29371290   PMID:29507755   PMID:29907679   PMID:30021884  
PMID:30639242   PMID:31012177   PMID:31980649   PMID:32225105   PMID:32955439  


Genomics

Comparative Map Data
PTPRG
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl361,561,569 - 62,297,609 (+)EnsemblGRCh38hg38GRCh38
GRCh38361,561,571 - 62,297,609 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37361,547,245 - 62,283,284 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36361,522,285 - 62,254,738 (+)NCBINCBI36hg18NCBI36
Build 34361,522,284 - 62,254,737NCBI
Celera361,560,149 - 62,297,663 (+)NCBI
Cytogenetic Map3p14.2NCBI
HuRef361,645,865 - 62,378,614 (+)NCBIHuRef
CHM1_1361,497,665 - 62,231,710 (+)NCBICHM1_1
Ptprg
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391410,227,722 - 10,916,341 (-)NCBIGRCm39mm39
GRCm381411,553,440 - 12,242,041 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1411,553,532 - 12,242,041 (+)EnsemblGRCm38mm10GRCm38
MGSCv371412,386,067 - 13,074,553 (+)NCBIGRCm37mm9NCBIm37
MGSCv361410,347,279 - 11,031,196 (+)NCBImm8
Celera147,168,551 - 7,867,137 (+)NCBICelera
Celera1415,457,844 - 15,462,854 (-)NCBICelera
Cytogenetic Map14A1NCBI
cM Map146.33NCBI
Ptprg
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21512,872,284 - 13,552,186 (-)NCBI
Rnor_6.0 Ensembl1512,926,167 - 13,228,607 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01512,926,056 - 13,633,839 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01516,953,275 - 17,647,626 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41514,449,352 - 15,130,760 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11514,449,351 - 14,966,931 (-)NCBI
Celera1512,868,965 - 13,547,381 (-)NCBICelera
Cytogenetic Map15p16NCBI
Ptprg
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049555173,676,342 - 4,352,909 (-)NCBIChiLan1.0ChiLan1.0
PTPRG
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1362,876,655 - 63,608,175 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl362,877,232 - 63,604,275 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0361,487,734 - 62,221,149 (+)NCBIMhudiblu_PPA_v0panPan3
PTPRG
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12028,777,306 - 29,481,097 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2028,778,386 - 29,481,145 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2028,705,294 - 29,408,229 (-)NCBI
ROS_Cfam_1.02029,011,902 - 29,715,647 (-)NCBI
UMICH_Zoey_3.12028,497,557 - 29,200,144 (-)NCBI
UNSW_CanFamBas_1.02028,855,762 - 29,559,818 (-)NCBI
UU_Cfam_GSD_1.02028,955,575 - 29,659,297 (-)NCBI
Ptprg
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118165,734,435 - 165,784,177 (-)NCBI
SpeTri2.0NW_0049366374,126,058 - 4,248,190 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PTPRG
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1343,548,770 - 43,869,270 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11343,132,786 - 43,869,843 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21347,543,401 - 47,873,302 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PTPRG
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12222,652,375 - 23,370,973 (+)NCBI
ChlSab1.1 Ensembl2223,061,935 - 23,370,960 (+)Ensembl
Ptprg
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248228,378,048 - 8,942,342 (+)NCBI

Position Markers
D3S1239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,059,768 - 62,059,952UniSTSGRCh37
Celera362,076,843 - 62,077,031UniSTS
Cytogenetic Map3p21-p14UniSTS
Marshfield Genetic Map382.24RGD
Marshfield Genetic Map382.24UniSTS
deCODE Assembly Map384.65UniSTS
Whitehead-YAC Contig Map3 UniSTS
SHGC-77036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,787,313 - 61,787,442UniSTSGRCh37
Build 36361,762,353 - 61,762,482RGDNCBI36
Celera361,800,193 - 61,800,322RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,886,243 - 61,886,372UniSTS
GeneMap99-GB4 RH Map3196.8UniSTS
SGC34642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,713,423 - 61,713,565UniSTSGRCh37
Build 36361,688,463 - 61,688,605RGDNCBI36
Celera361,726,331 - 61,726,473RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,812,416 - 61,812,558UniSTS
GeneMap99-GB4 RH Map3192.75UniSTS
Whitehead-RH Map3231.2UniSTS
NCBI RH Map3547.2UniSTS
D3S4059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,894,495 - 61,894,611UniSTSGRCh37
Build 36361,869,535 - 61,869,651RGDNCBI36
Celera361,911,508 - 61,911,624RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,992,989 - 61,993,105UniSTS
SHGC-77063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,663,234 - 61,663,360UniSTSGRCh37
Build 36361,638,274 - 61,638,400RGDNCBI36
Celera361,676,136 - 61,676,262RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,762,472 - 61,762,598UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
Whitehead-RH Map3231.5UniSTS
SHGC-32613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,783,423 - 61,783,572UniSTSGRCh37
Build 36361,758,463 - 61,758,612RGDNCBI36
Celera361,796,303 - 61,796,452RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,882,353 - 61,882,502UniSTS
Stanford-G3 RH Map32851.0UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
Whitehead-RH Map3229.7UniSTS
NCBI RH Map3596.4UniSTS
GeneMap99-G3 RH Map32749.0UniSTS
STS-T47142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,096,228 - 62,096,465UniSTSGRCh37
Build 36362,071,268 - 62,071,505RGDNCBI36
Celera362,113,300 - 62,113,537RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,194,285 - 62,194,522UniSTS
GeneMap99-GB4 RH Map3197.21UniSTS
RH11441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,109,559 - 62,109,661UniSTSGRCh37
GRCh3728,824,030 - 8,824,132UniSTSGRCh37
Build 3628,741,481 - 8,741,583RGDNCBI36
Celera28,737,820 - 8,737,922RGD
Celera362,126,632 - 62,126,734UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map3p21-p14UniSTS
Cytogenetic Map3p14.2UniSTS
HuRef28,670,214 - 8,670,316UniSTS
HuRef362,207,616 - 62,207,718UniSTS
SHGC-58561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,162,332 - 62,162,440UniSTSGRCh37
Build 36362,137,372 - 62,137,480RGDNCBI36
Celera362,179,402 - 62,179,510RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,260,378 - 62,260,486UniSTS
TNG Radiation Hybrid Map338423.0UniSTS
RH104179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,791,047 - 61,791,179UniSTSGRCh37
Build 36361,766,087 - 61,766,219RGDNCBI36
Celera361,803,927 - 61,804,059RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,889,977 - 61,890,109UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
SHGC-80756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,222,782 - 62,223,092UniSTSGRCh37
Build 36362,197,822 - 62,198,132RGDNCBI36
Celera362,239,860 - 62,240,170RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,320,812 - 62,321,122UniSTS
TNG Radiation Hybrid Map338477.0UniSTS
SHGC-86248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,909,781 - 61,910,051UniSTSGRCh37
Build 36361,884,821 - 61,885,091RGDNCBI36
Celera361,926,786 - 61,927,056RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,008,268 - 62,008,538UniSTS
RH123043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,197,898 - 62,198,204UniSTSGRCh37
Build 36362,172,938 - 62,173,244RGDNCBI36
Celera362,215,000 - 62,215,306RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,295,927 - 62,296,233UniSTS
TNG Radiation Hybrid Map338449.0UniSTS
G63034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,844,391 - 61,844,697UniSTSGRCh37
Build 36361,819,431 - 61,819,737RGDNCBI36
Celera361,861,329 - 61,861,635RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,942,958 - 61,943,264UniSTS
D2S208E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,109,221 - 62,109,366UniSTSGRCh37
GRCh3728,824,325 - 8,824,462UniSTSGRCh37
Build 3628,741,776 - 8,741,913RGDNCBI36
Celera28,738,115 - 8,738,252RGD
Celera362,126,294 - 62,126,439UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map3p21-p14UniSTS
Cytogenetic Map3p14.2UniSTS
HuRef28,670,509 - 8,670,646UniSTS
HuRef362,207,278 - 62,207,423UniSTS
SHGC-156251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,920,598 - 61,920,905UniSTSGRCh37
Build 36361,895,638 - 61,895,945RGDNCBI36
Celera361,937,670 - 61,937,977RGD
Cytogenetic Map3p21-p14UniSTS
SHGC-79619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,145,413 - 62,145,690UniSTSGRCh37
Build 36362,120,453 - 62,120,730RGDNCBI36
Celera362,162,487 - 62,162,764RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,243,470 - 62,243,747UniSTS
TNG Radiation Hybrid Map338400.0UniSTS
D3S4021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,048,104 - 62,048,256UniSTSGRCh37
Build 36362,023,144 - 62,023,296RGDNCBI36
Celera362,065,185 - 62,065,337RGD
HuRef362,146,553 - 62,146,705UniSTS
D3S4099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,666,902 - 61,667,173UniSTSGRCh37
Build 36361,641,942 - 61,642,213RGDNCBI36
Celera361,679,804 - 61,680,075RGD
HuRef361,765,870 - 61,766,141UniSTS
D3S4100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,794,425 - 61,794,681UniSTSGRCh37
Build 36361,769,465 - 61,769,721RGDNCBI36
Celera361,807,305 - 61,807,561RGD
HuRef361,893,355 - 61,893,611UniSTS
D3S4101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,103,406 - 62,103,609UniSTSGRCh37
Build 36362,078,446 - 62,078,649RGDNCBI36
Celera362,120,478 - 62,120,681RGD
HuRef362,201,464 - 62,201,667UniSTS
D3S4334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,040,204 - 62,040,303UniSTSGRCh37
Build 36362,015,244 - 62,015,343RGDNCBI36
Celera362,057,287 - 62,057,386RGD
HuRef362,138,657 - 62,138,756UniSTS
SHGC-77060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,665,966 - 61,666,061UniSTSGRCh37
Build 36361,641,006 - 61,641,101RGDNCBI36
Celera361,678,868 - 61,678,963RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,765,204 - 61,765,299UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
D3S4048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,005,330 - 62,005,434UniSTSGRCh37
Build 36361,980,370 - 61,980,474RGDNCBI36
Celera362,022,399 - 62,022,503RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,103,755 - 62,103,859UniSTS
STS-T78588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,784,341 - 61,784,576UniSTSGRCh37
Build 36361,759,381 - 61,759,616RGDNCBI36
Celera361,797,221 - 61,797,456RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,883,271 - 61,883,506UniSTS
GeneMap99-GB4 RH Map3196.7UniSTS
SHGC-77046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,279,450 - 62,279,623UniSTSGRCh37
Build 36362,254,490 - 62,254,663RGDNCBI36
Celera362,296,540 - 62,296,713RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,377,491 - 62,377,664UniSTS
TNG Radiation Hybrid Map338516.0UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
Whitehead-RH Map3229.7UniSTS
RH67912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,109,873 - 62,110,076UniSTSGRCh37
GRCh3728,822,502 - 8,823,034UniSTSGRCh37
Build 3628,739,953 - 8,740,485RGDNCBI36
Celera28,736,292 - 8,736,824RGD
Celera362,126,946 - 62,127,149UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map3p21-p14UniSTS
Cytogenetic Map3p14.2UniSTS
HuRef28,668,686 - 8,669,218UniSTS
HuRef362,207,930 - 62,208,133UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
D3S4045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,047,997 - 62,048,210UniSTSGRCh37
Build 36362,023,037 - 62,023,250RGDNCBI36
Celera362,065,078 - 62,065,291RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,146,446 - 62,146,659UniSTS
RH12127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,247,550 - 62,247,670UniSTSGRCh37
Build 36362,222,590 - 62,222,710RGDNCBI36
Celera362,264,626 - 62,264,746RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,345,579 - 62,345,699UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
NCBI RH Map3559.9UniSTS
SHGC-56789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,578,345 - 61,578,439UniSTSGRCh37
Build 36361,553,385 - 61,553,479RGDNCBI36
Celera361,591,247 - 61,591,341RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,676,937 - 61,677,031UniSTS
TNG Radiation Hybrid Map338170.0UniSTS
D3S3448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,048,072 - 62,048,250UniSTSGRCh37
Build 36362,023,112 - 62,023,290RGDNCBI36
Celera362,065,153 - 62,065,331RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,146,521 - 62,146,699UniSTS
D3S3934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,279,140 - 62,279,260UniSTSGRCh37
Build 36362,254,180 - 62,254,300RGDNCBI36
Celera362,296,230 - 62,296,350RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,377,181 - 62,377,301UniSTS
Whitehead-YAC Contig Map3 UniSTS
RH70195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,713,421 - 61,713,619UniSTSGRCh37
Build 36361,688,461 - 61,688,659RGDNCBI36
Celera361,726,329 - 61,726,527RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,812,414 - 61,812,612UniSTS
GeneMap99-GB4 RH Map3196.8UniSTS
G31070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,868,015 - 61,868,152UniSTSGRCh37
Build 36361,843,055 - 61,843,192RGDNCBI36
Celera361,884,948 - 61,885,085RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,966,575 - 61,966,712UniSTS
D3S4003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,109,535 - 62,109,943UniSTSGRCh37
Build 36362,084,575 - 62,084,983RGDNCBI36
Celera362,126,608 - 62,127,016RGD
Cytogenetic Map2p25UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p21-p14UniSTS
HuRef362,207,592 - 62,208,000UniSTS
TNG Radiation Hybrid Map338373.0UniSTS
Stanford-G3 RH Map32855.0UniSTS
Whitehead-YAC Contig Map3 UniSTS
NCBI RH Map3596.4UniSTS
GeneMap99-G3 RH Map32753.0UniSTS
D3S4211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,107,801 - 62,107,944UniSTSGRCh37
Build 36362,082,841 - 62,082,984RGDNCBI36
Celera362,124,874 - 62,125,017RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,205,858 - 62,206,001UniSTS
Stanford-G3 RH Map32859.0UniSTS
NCBI RH Map3596.4UniSTS
GeneMap99-G3 RH Map32757.0UniSTS
G29177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37361,784,331 - 61,784,478UniSTSGRCh37
Build 36361,759,371 - 61,759,518RGDNCBI36
Celera361,797,211 - 61,797,358RGD
Cytogenetic Map3p21-p14UniSTS
HuRef361,883,261 - 61,883,408UniSTS
D3S4073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37362,047,996 - 62,048,244UniSTSGRCh37
Build 36362,023,036 - 62,023,284RGDNCBI36
Celera362,065,077 - 62,065,325RGD
Cytogenetic Map3p21-p14UniSTS
HuRef362,146,445 - 62,146,693UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR624hsa-miR-624-5pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:2191
Count of miRNA genes:957
Interacting mature miRNAs:1196
Transcripts:ENST00000295874, ENST00000468576, ENST00000474889, ENST00000475012, ENST00000475527, ENST00000485215, ENST00000495879
Prediction methods:Microtar, 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
Medium 746 1357 905 64 135 56 2215 347 709 197 638 1324 13 1125 1265 1
Low 1674 875 817 558 698 408 2138 1843 3017 218 808 267 158 1 79 1523 3
Below cutoff 7 735 1 1010 1 6 3 10 15 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001375471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017006964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC096919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC098482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC105939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH006632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI872451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC036018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC048961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC140904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU273472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L09247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X54132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000295874   ⟹   ENSP00000295874
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl361,561,911 - 62,293,329 (+)Ensembl
RefSeq Acc Id: ENST00000468576
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl362,243,805 - 62,263,465 (+)Ensembl
RefSeq Acc Id: ENST00000474889   ⟹   ENSP00000418112
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl361,561,571 - 62,297,609 (+)Ensembl
RefSeq Acc Id: ENST00000475012
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl362,217,583 - 62,293,551 (+)Ensembl
RefSeq Acc Id: ENST00000475527
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl361,561,851 - 61,751,049 (+)Ensembl
RefSeq Acc Id: ENST00000485215
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl362,243,576 - 62,267,813 (+)Ensembl
RefSeq Acc Id: ENST00000495879
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl361,561,569 - 61,771,395 (+)Ensembl
RefSeq Acc Id: NM_001375471   ⟹   NP_001362400
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,571 - 62,297,609 (+)NCBI
RefSeq Acc Id: NM_002841   ⟹   NP_002832
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,571 - 62,297,609 (+)NCBI
GRCh37361,547,243 - 62,280,573 (+)ENTREZGENE
Build 36361,522,285 - 62,254,738 (+)NCBI Archive
HuRef361,645,865 - 62,378,614 (+)ENTREZGENE
CHM1_1361,497,665 - 62,231,710 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006961   ⟹   XP_016862450
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,571 - 62,297,609 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006962   ⟹   XP_016862451
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,748,025 - 62,297,609 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006963   ⟹   XP_016862452
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,571 - 62,297,609 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017006964   ⟹   XP_016862453
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,636,667 - 62,297,609 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002832   ⟸   NM_002841
- Peptide Label: isoform 1 precursor
- UniProtKB: P23470 (UniProtKB/Swiss-Prot),   Q49A02 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016862450   ⟸   XM_017006961
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016862452   ⟸   XM_017006963
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016862453   ⟸   XM_017006964
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_016862451   ⟸   XM_017006962
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: NP_001362400   ⟸   NM_001375471
- Peptide Label: isoform 2
RefSeq Acc Id: ENSP00000295874   ⟸   ENST00000295874
RefSeq Acc Id: ENSP00000418112   ⟸   ENST00000474889
Promoters
RGD ID:6801493
Promoter ID:HG_KWN:45404
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid,   NB4
Transcripts:ENST00000394461,   ENST00000394462,   NM_002841,   UC003DLA.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36361,521,441 - 61,522,222 (+)MPROMDB
RGD ID:6864854
Promoter ID:EPDNEW_H5592
Type:initiation region
Name:PTPRG_3
Description:protein tyrosine phosphatase, receptor type G
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5593  EPDNEW_H5594  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,030 - 61,561,090EPDNEW
RGD ID:6864856
Promoter ID:EPDNEW_H5593
Type:initiation region
Name:PTPRG_1
Description:protein tyrosine phosphatase, receptor type G
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5592  EPDNEW_H5594  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,571 - 61,561,631EPDNEW
RGD ID:6864858
Promoter ID:EPDNEW_H5594
Type:initiation region
Name:PTPRG_2
Description:protein tyrosine phosphatase, receptor type G
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5592  EPDNEW_H5593  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38361,561,845 - 61,561,905EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p14.2-14.1(chr3:61970847-68465832)x1 copy number loss See cases [RCV000050774] Chr3:61970847..68465832 [GRCh38]
Chr3:61956521..68514983 [GRCh37]
Chr3:61931561..68597673 [NCBI36]
Chr3:3p14.2-14.1
pathogenic
GRCh38/hg38 3p21.1-14.1(chr3:54045018-66060461)x1 copy number loss See cases [RCV000051081] Chr3:54045018..66060461 [GRCh38]
Chr3:54079045..66046136 [GRCh37]
Chr3:54054085..66021176 [NCBI36]
Chr3:3p21.1-14.1
pathogenic
NM_002841.3(PTPRG):c.654C>T (p.Ile218=) single nucleotide variant Malignant melanoma [RCV000066175] Chr3:62132640 [GRCh38]
Chr3:62118314 [GRCh37]
Chr3:62093354 [NCBI36]
Chr3:3p14.2
not provided
NM_002841.3(PTPRG):c.2194C>T (p.Pro732Ser) single nucleotide variant Malignant melanoma [RCV000066176] Chr3:62218889 [GRCh38]
Chr3:62204563 [GRCh37]
Chr3:62179603 [NCBI36]
Chr3:3p14.2
not provided
NM_002841.3(PTPRG):c.190+91271A>T single nucleotide variant Lung cancer [RCV000093623] Chr3:61840253 [GRCh38]
Chr3:61825927 [GRCh37]
Chr3:3p14.2
uncertain significance
NM_002841.3(PTPRG):c.519+14225C>T single nucleotide variant Lung cancer [RCV000093625] Chr3:62017722 [GRCh38]
Chr3:62003396 [GRCh37]
Chr3:3p14.2
uncertain significance
GRCh38/hg38 3p14.3-14.1(chr3:57430538-64884522)x1 copy number loss See cases [RCV000139570] Chr3:57430538..64884522 [GRCh38]
Chr3:57416265..64870197 [GRCh37]
Chr3:57391305..64845237 [NCBI36]
Chr3:3p14.3-14.1
pathogenic
GRCh38/hg38 3p14.3-11.1(chr3:57140424-90259960)x1 copy number loss See cases [RCV000139626] Chr3:57140424..90259960 [GRCh38]
Chr3:57174452..90309110 [GRCh37]
Chr3:57149492..90391800 [NCBI36]
Chr3:3p14.3-11.1
pathogenic
GRCh37/hg19 3p14.2-14.1(chr3:60526226-63742930)x1 copy number loss See cases [RCV000511529] Chr3:60526226..63742930 [GRCh37]
Chr3:3p14.2-14.1
likely pathogenic
GRCh37/hg19 3p14.2(chr3:61036291-61639996)x3 copy number gain See cases [RCV000511038] Chr3:61036291..61639996 [GRCh37]
Chr3:3p14.2
uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p14.2(chr3:61546425-61547951)x0 copy number loss not provided [RCV000742458] Chr3:61546425..61547951 [GRCh37]
Chr3:3p14.2
benign
GRCh37/hg19 3p14.2(chr3:61600528-61688641)x3 copy number gain not provided [RCV000742459] Chr3:61600528..61688641 [GRCh37]
Chr3:3p14.2
benign
GRCh37/hg19 3p14.2(chr3:61699969-61907965)x1 copy number loss not provided [RCV000742460] Chr3:61699969..61907965 [GRCh37]
Chr3:3p14.2
benign
GRCh37/hg19 3p14.2(chr3:61741051-61788620)x3 copy number gain not provided [RCV000742461] Chr3:61741051..61788620 [GRCh37]
Chr3:3p14.2
benign
NM_002841.4(PTPRG):c.774A>G (p.Thr258=) single nucleotide variant not provided [RCV000900809] Chr3:62157158 [GRCh38]
Chr3:62142832 [GRCh37]
Chr3:3p14.2
likely benign
NM_002841.4(PTPRG):c.1287C>T (p.Asn429=) single nucleotide variant not provided [RCV000900810] Chr3:62195130 [GRCh38]
Chr3:62180804 [GRCh37]
Chr3:3p14.2
likely benign
NM_002841.4(PTPRG):c.1299C>T (p.Ser433=) single nucleotide variant not provided [RCV000938868] Chr3:62195142 [GRCh38]
Chr3:62180816 [GRCh37]
Chr3:3p14.2
likely benign
GRCh37/hg19 3p14.2-14.1(chr3:60844727-63983596)x1 copy number loss not provided [RCV000845843] Chr3:60844727..63983596 [GRCh37]
Chr3:3p14.2-14.1
uncertain significance
GRCh37/hg19 3p14.2-14.1(chr3:62206958-63944889)x3 copy number gain not provided [RCV001005440] Chr3:62206958..63944889 [GRCh37]
Chr3:3p14.2-14.1
uncertain significance
GRCh37/hg19 3p14.3-14.1(chr3:57076136-65716956)x1 copy number loss not provided [RCV000846379] Chr3:57076136..65716956 [GRCh37]
Chr3:3p14.3-14.1
pathogenic
NM_002841.4(PTPRG):c.1236T>C (p.His412=) single nucleotide variant not provided [RCV000883118] Chr3:62195079 [GRCh38]
Chr3:62180753 [GRCh37]
Chr3:3p14.2
benign
NM_002841.4(PTPRG):c.3262G>A (p.Val1088Ile) single nucleotide variant not provided [RCV000886165] Chr3:62273025 [GRCh38]
Chr3:62258700 [GRCh37]
Chr3:3p14.2
benign
NM_002841.4(PTPRG):c.40C>T (p.Leu14=) single nucleotide variant not provided [RCV000879954] Chr3:61562327 [GRCh38]
Chr3:61548001 [GRCh37]
Chr3:3p14.2
benign
NM_002841.4(PTPRG):c.174G>A (p.Pro58=) single nucleotide variant not provided [RCV000956110] Chr3:61748966 [GRCh38]
Chr3:61734640 [GRCh37]
Chr3:3p14.2
benign
GRCh37/hg19 3p14.2-14.1(chr3:60449667-65561638)x1 copy number loss not provided [RCV001005439] Chr3:60449667..65561638 [GRCh37]
Chr3:3p14.2-14.1
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9671 AgrOrtholog
COSMIC PTPRG COSMIC
Ensembl Genes ENSG00000144724 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000295874 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000418112 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000295874 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000474889 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot
  3.10.200.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.90.190.10 UniProtKB/Swiss-Prot
GTEx ENSG00000144724 GTEx
HGNC ID HGNC:9671 ENTREZGENE
Human Proteome Map PTPRG Human Proteome Map
InterPro alpha_CARP_receptor-type UniProtKB/Swiss-Prot
  CA_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CA_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Carbonic_anhydrase_a-class UniProtKB/TrEMBL
  Carbonic_anhydrase_CA15 UniProtKB/TrEMBL
  FN3_dom UniProtKB/Swiss-Prot
  FN3_sf UniProtKB/Swiss-Prot
  Ig-like_fold UniProtKB/Swiss-Prot
  Prot-tyrosine_phosphatase-like UniProtKB/Swiss-Prot
  PTPase_domain UniProtKB/Swiss-Prot
  Tyr_Pase_AS UniProtKB/Swiss-Prot
  Tyr_Pase_cat UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_dom UniProtKB/Swiss-Prot
KEGG Report hsa:5793 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 5793 ENTREZGENE
OMIM 176886 OMIM
PANTHER PTHR18952 UniProtKB/TrEMBL
  PTHR18952:SF134 UniProtKB/TrEMBL
Pfam Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  fn3 UniProtKB/Swiss-Prot
  Y_phosphatase UniProtKB/Swiss-Prot
PharmGKB PA34016 PharmGKB, RGD
PRINTS PRTYPHPHTASE UniProtKB/Swiss-Prot
PROSITE ALPHA_CA_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FN3 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_1 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_2 UniProtKB/Swiss-Prot
  TYR_PHOSPHATASE_PTP UniProtKB/Swiss-Prot
SMART Carb_anhydrase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FN3 UniProtKB/Swiss-Prot
  PTPc UniProtKB/Swiss-Prot
  PTPc_motif UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49265 UniProtKB/Swiss-Prot
  SSF51069 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52799 UniProtKB/Swiss-Prot
UniProt L8E7E6_HUMAN UniProtKB/TrEMBL
  O60420_HUMAN UniProtKB/TrEMBL
  P23470 ENTREZGENE, UniProtKB/Swiss-Prot
  Q49A02 ENTREZGENE, UniProtKB/TrEMBL
  Q86TJ8_HUMAN UniProtKB/TrEMBL
UniProt Secondary B2RU12 UniProtKB/Swiss-Prot
  B7ZLX5 UniProtKB/Swiss-Prot
  Q15623 UniProtKB/Swiss-Prot
  Q59EE0 UniProtKB/Swiss-Prot
  Q68DU5 UniProtKB/Swiss-Prot


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