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PTPN2 (protein tyrosine phosphatase non-receptor type 2)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5771
Gene nameGene Name - the full gene name approved by the HGNC.
Protein tyrosine phosphatase non-receptor type 2
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PTPN2
SynonymsGene synonyms aliases
PTN2, PTPT, TC-PTP, TC45, TC48, TCELLPTP, TCPTP
ChromosomeChromosome number
18
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18p11.21
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT054248 hsa-miR-210-3p Chip, Luciferase reporter assay, QRTPCR, Western blot 23579275
MIRT450163 hsa-miR-1264 PAR-CLIP 22100165
MIRT450162 hsa-miR-520d-5p PAR-CLIP 22100165
MIRT450161 hsa-miR-524-5p PAR-CLIP 22100165
MIRT450163 hsa-miR-1264 HITS-CLIP 27418678
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0004725 Function Protein tyrosine phosphatase activity EXP 12138178
GO:0004725 Function Protein tyrosine phosphatase activity IDA 12612081
GO:0004725 Function Protein tyrosine phosphatase activity IMP 11909529, 14966296
GO:0004726 Function Non-membrane spanning protein tyrosine phosphatase activity IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P17706
Protein name Tyrosine-protein phosphatase non-receptor type 2 (EC 3.1.3.48) (T-cell protein-tyrosine phosphatase) (TCPTP)
Protein function Non-receptor type tyrosine-specific phosphatase that dephosphorylates receptor protein tyrosine kinases including INSR, EGFR, CSF1R, PDGFR. Also dephosphorylates non-receptor protein tyrosine kinases like JAK1, JAK2, JAK3, Src family kinases, ST
PDB 1L8K , 6ZZ4 , 7F5N , 7F5O , 7UAD , 8U0H , 8UH6 , 9C54 , 9C55 , 9C56
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00102 Y_phosphatase
42 274
Protein-tyrosine phosphatase
Domain
Sequence
MPTTIEREFEELDTQRRWQPLYLEIRNESHDYPHRVAKFPENRNRNRYRDVSPYDHSRVK
LQNAENDYINASLVDIEEAQRSYILTQGPLPNTCCHFWLMVWQQKTKAVVMLNRIVEKES
VKCAQYWPTDDQEMLFKETGFSVKLLSEDVKSYYTVHLLQLENINSGETRTISHFHYTTW
PDFGVPESPASFLNFLFKVRESGSLNPDHGPAVIHCSAGIGRSGTFSLVDTCLVLMEKGD
DINIKQVLLNMRKYRMGLIQTPDQLRFSYMAIIE
GAKCIKGDSSIQKRWKELSKEDLSPA
FDHSPNKIMTEKYNGNRIGLEEEKLTGDRCTGLSSKMQDTMEENSESALRKRIREDRKAT
TAQKVQQMKQRLNENERKRKRWLYWQPILTKMGFMSVILVGAFVGWTLFFQQNAL
Sequence length 415
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  JAK-STAT signaling pathway   Negative regulation of MET activity
Regulation of IFNG signaling
Interleukin-37 signaling
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Apraxia Apraxias rs121908377, rs121908378, rs1135401820, rs1178491246, rs1584969672
Arthritis Systemic onset juvenile chronic arthritis, Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 23603761, 22354554
Asthma Asthma rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 21150878
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs41285370, rs869025224 21383967, 30595370, 30595370
Unknown
Disease name Disease term dbSNP ID References
Ankylosing spondylitis Ankylosing spondylitis 26974007
Celiac disease Celiac Disease rs2305764, rs35218876 23143596, 26546613, 22057235, 20190752
Cholangitis Cholangitis, Sclerosing 26974007
Crohn disease Crohn Disease, Regional enteritis, NON RARE IN EUROPE: Crohn disease rs2066847, rs2066844, rs886052047, rs5743265, rs111608429, rs104895438 18587394, 25489960, 21102463, 26974007, 28067908, 26192919, 17554261, 21298027, 17554261

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