PTPN6 - protein tyrosine phosphatase non-receptor type 6 Gene

Also Known as HCP; HCPH; SHP1; SHP-1; HPTP1C; PTP-1C; SHP-1L; SH-PTP1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5777

About PTPN6

Cytogenetic location: 12p13.31 Genomic coordinates (GRCh38): 12:6,946,577-6,961,316 (from NCBI)

This gene has 23 transcripts (splice variants), 198 orthologues, 35 paralogues and is associated with 61 phenotypes. Broad expression in spleen (RPKM 76.2), lymph node (RPKM 74.9) and 19 other tissues.

Summary

The protein encoded by this gene is a member of the protein tyrosine Phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. N-terminal part of this PTP contains two tandem Src homolog (SH2) domains, which act as protein phospho-tyrosine binding domains, and mediate the interaction of this PTP with its substrates. This PTP is expressed primarily in hematopoietic cells, and functions as an important regulator of multiple signaling pathways in hematopoietic cells. This PTP has been shown to interact with, and dephosphorylate a wide spectrum of phospho-proteins involved in hematopoietic cell signaling. Multiple alternatively spliced variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jul 2008]

PTPN6 Products (3)

mRNA Protein Name
NM_002831.6 NP_002822.2 tyrosine-protein phosphatase non-receptor type 6 isoform 1
NM_080548.5 NP_536858.1 tyrosine-protein phosphatase non-receptor type 6 isoform 2
NM_080549.4 NP_536859.1 tyrosine-protein phosphatase non-receptor type 6 isoform 3
Molecular Function GO Annotation Evidence References Source
enables phosphorylation-dependent protein binding IPI
IPI: Inferred from physical interaction
11162587 GOA
enables phosphotyrosine residue binding IPI
IPI: Inferred from physical interaction
11986327 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7228577 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
11266449 GOA
enables protein tyrosine phosphatase activity IDA
IDA: Inferred from direct assay
17562706 GOA
enables protein tyrosine phosphatase activity IMP
IMP: Inferred from mutant phenotype
10206955 GOA
enables transmembrane receptor protein tyrosine phosphatase activity IDA
IDA: Inferred from direct assay
11266449 GOA
Biological Process GO Annotation Evidence References Source
involved in CD27 signaling pathway IDA
IDA: Inferred from direct assay
38354704 GOA
involved in T cell activation IDA
IDA: Inferred from direct assay
38354704 GOA
involved in cell differentiation IDA
IDA: Inferred from direct assay
11266449 GOA
involved in negative regulation of B cell receptor signaling pathway IDA
IDA: Inferred from direct assay
35941532 GOA
involved in negative regulation of angiogenesis IDA
IDA: Inferred from direct assay
23896411 GOA
involved in negative regulation of inflammatory response to wounding IDA
IDA: Inferred from direct assay
27830702 GOA
involved in negative regulation of innate immune response IDA
IDA: Inferred from direct assay
34811497 GOA
involved in negative regulation of peptidyl-tyrosine phosphorylation IMP
IMP: Inferred from mutant phenotype
19749791 GOA
involved in peptidyl-tyrosine dephosphorylation IMP
IMP: Inferred from mutant phenotype
17562706 GOA
involved in peptidyl-tyrosine phosphorylation IDA
IDA: Inferred from direct assay
9285411 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
19749791 GOA
involved in positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction IMP
IMP: Inferred from mutant phenotype
19838216 GOA
involved in protein dephosphorylation IDA
IDA: Inferred from direct assay
11266449 GOA
involved in regulation of ERK1 and ERK2 cascade IDA
IDA: Inferred from direct assay
11266449 GOA
involved in regulation of G1/S transition of mitotic cell cycle IMP
IMP: Inferred from mutant phenotype
19838216 GOA
Cellular Component GO Annotation Evidence References Source
is active in cytoplasm IDA
IDA: Inferred from direct assay
9065461 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
10940933 GOA
located in nucleus IDA
IDA: Inferred from direct assay
19838216 GOA
is active in plasma membrane IDA
IDA: Inferred from direct assay
23896411 GOA
part of protein-containing complex IMP
IMP: Inferred from mutant phenotype
17562706 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PTPN6 Protein Structure

SH2

SH2: SH2 domain (4 - 79)

SH2

SH2: SH2 domain (110 - 194)

Y_phosphatase

Y_phosphatase: Protein-tyrosine phosphatase (270 - 513)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 595 a.a.
Protein Preferred Names Protein Names

tyrosine-protein phosphatase non-receptor type 6

  • hematopoietic cell phosphatase

PTPN6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PTPN6 P29350 KDR Homo sapiens P35968 28065597
Intra
PTPN6 P29350 LCK Homo sapiens P06239 8114715
Intra
PTPN6 P29350 NFAT5 Homo sapiens O94916-1 20351292
Intra
PTPN6 P29350 NFAT5 Homo sapiens O94916-1 20351292
Intra
PTPN6 P29350 PTPN12 Homo sapiens Q05209 31980649
Intra
PTPN6 P29350 PTPN12 Homo sapiens Q05209 33961781
Intra
PTPN6 P29350 LILRB4 Homo sapiens Q8NHJ6 18802077
Intra
PTPN6 P29350 LILRB1 Homo sapiens Q8NHL6 18802077
Intra
PTPN6 P29350 LILRB2 Homo sapiens Q8N423 18802077
Intra
PTPN6 P29350 LILRB3 Homo sapiens O75022 18802077
Intra
PTPN6 P29350 THEMIS Homo sapiens Q8N1K5 25535246
Intra
PTPN6 P29350 CD33 Homo sapiens P20138 10206955
Intra
PTPN6 P29350 CD33 Homo sapiens P20138 10556798
Intra
PTPN6 P29350 CD33 Homo sapiens P20138 10556798
Intra
PTPN6 P29350 IGF1R Homo sapiens P08069 28065597
Intra
PTPN6 P29350 CD37 Homo sapiens P11049 22624718
Intra
PTPN6 P29350 EPOR Homo sapiens P19235 7228577
Intra
PTPN6 P29350 EPOR Homo sapiens P19235 7228577
Intra
PTPN6 P29350 EPOR Homo sapiens P19235 7528577
Cross
PTPN6 P29350 tir Escherichia coli O157:H7 Q7DB77 23001144
Intra
PTPN6 P29350 PECAM1 Homo sapiens P16284 9774457
Intra
PTPN6 P29350 PECAM1 Homo sapiens P16284
SPR
9774457
Intra
PTPN6 P29350 FCGR2B Homo sapiens P31994 8577729
Intra
PTPN6 P29350 FCGR2B Homo sapiens P31994 9148918
Intra
PTPN6 P29350 ROS1 Homo sapiens P08922 11266449
Intra
PTPN6 P29350 ROS1 Homo sapiens P08922 11266449
Intra
PTPN6 P29350 FHL3 Homo sapiens Q13643 25416956
Intra
PTPN6 P29350 CASP8 Homo sapiens Q14790 18086677
Intra
PTPN6 P29350 CASP8 Homo sapiens Q14790 18086677
Intra
PTPN6 P29350 KIR2DL3 Homo sapiens P43628 8691154
Intra
PTPN6 P29350 KIR2DL3 Homo sapiens P43628 8648092
Intra
PTPN6 P29350 KIR2DL3 Homo sapiens P43628 9148918
Intra
PTPN6 P29350 KIR2DL1 Homo sapiens P43626 8691146
Intra
PTPN6 P29350 KIR2DL1 Homo sapiens P43626 8691146
Intra
PTPN6 P29350 PILRA Homo sapiens Q9UKJ1
SPR
10660620
Intra
PTPN6 P29350 PILRA Homo sapiens Q9UKJ1
Y2H
10660620
Intra
PTPN6 P29350 LAIR1 Homo sapiens Q6GTX8 10764762
Intra
PTPN6 P29350 LAIR1 Homo sapiens Q6GTX8
Y2H
10660620
Intra
PTPN6 P29350 LAIR1 Homo sapiens Q6GTX8 10764762
Cross
PTPN6 P29350 tir Escherichia coli O127:H6 B7UM99 23001144
Cross
PTPN6 P29350 Ppp1r9b Rattus norvegicus O35274 25785436
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant PTPN6 Proteins

Cat. No. Product Name Accession Purity
HY-P71141 SHP-1 Protein, Human (His) AAH02523.1 (K243-I541) ≥ 95%, as determined by reducing SDS-PAGE.

PTPN6 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81307 SHP1 Antibody (YA1044) WB, IP Human
HY-P81307A SHP1 Antibody (YA1045) WB, IHC-P, ICC/IF, FC Human
HY-P81307AA SHP1 Antibody (YA1045)(PBS only) WB, IHC-P, ICC/IF, FC Human
HY-P84244 SHP1 Antibody (YA3941) ICC/IF, FC, ELISA Human
HY-P84244A SHP1 Antibody (YA3941)(PBS only) ICC/IF, FC, ELISA Human

Related Diseases

Diseases Alias
Polycythemia
  • Erythrocythemia

  • Polycythemia Vera

  • Polycythaemia Due To High Altitude

Polycythemia Vera
  • PV

  • Polycythemia Rubra Vera

  • Prv

  • Osler-Vaquez Disease

  • Chronic Erythremia

  • Polycythaemia Rubra Vera

  • Primary Polycythemia

  • Vaquez Disease

  • Polycythemia Vera, Somatic

  • Osler-Vaquez Syndrome

  • Proliferative Polycythaemia

  • Polycythemia Ruba Vera

  • Acquired Primary Erythrocytosis

  • Heilmeyer-Schoner Disease

  • Vaquez Osler Disease

  • Primary Polycythaemia

Neutrophilic Dermatosis, Acute Febrile
  • Sweet Syndrome

  • Acute Febrile Neutrophilic Dermatosis

  • Ss

  • AFND

  • Pyrin-Associated Autoinflammatory Disease

  • PAAND

  • Gomm-Button Disease

  • Sweet'S Syndrome

  • Gomm Button Disease

  • Sweets Syndrome

  • Acromelic Frontonasal Dysostosis

  • Sweet Disease

Severe Congenital Neutropenia
  • Congenital Neutropenia

  • Neutropenia, Severe Congenital

  • Congenital Agranulocytosis

  • Infantile Genetic Agranulocytosis

  • Kostmann Disease

  • Kostmann'S Agranulocytosis

  • Kostmann'S Syndrome

  • Severe Infantile Genetic Neutropenia

Acute Promyelocytic Leukemia
  • Leukemia, Acute Promyelocytic

  • Acute Myeloblastic Leukemia Type 3

  • Aml M3

  • APL

  • Leukemia, Acute Promyelocytic, Somatic

  • Aml With T(15

  • 17)(Q22

  • Q12)

  • (Pml/Raralpha) And Variants

  • Apml

  • Acute Myeloblastic Leukemia 3

  • Acute Myeloid Leukemia With T(15

  • 17)(Q22

  • Q12)

  • (Pml/Raralpha) And Variants

  • Acute Myeloblastic Leukaemia Type 3

  • Acute Myeloid Leukaemia M3

  • Acute Myeloid Leukemia M3

  • Acute Promyelocytic Leukaemia

  • M3 Anll

  • Myeloid Leukemia, Acute, M3

  • Leukemia Promyelocytic Acute

  • Leukemia, Promyelocytic, Acute

  • Leukemia, Acute, Promyelocytic

Erythrocytosis, Familial, 1
  • ECYT1

  • Pfcp

  • Primary Familial And Congenital Polycythemia

  • Familial Erythrocytosis 1

  • Familial Erythrocytosis

  • Polycythemia, Primary Familial And Congenital

  • Autosomal Dominant Benign Erythrocytosis

  • Familial Erythrocytosis Type 1

  • Congenital Erythrocytosis Due To Erythropoietin Receptor Mutation

  • Congenital Polycythemia Due To Erythropoietin Receptor Mutation

  • Primary Congenital Erythrocytosis

  • Primary Familial Polycythemia

  • Erythrocytosis, Autosomal Dominant Benign

  • Erythrocytosis, Somatic

  • Autosomal Dominant Familial Erythrocytosis-1

  • Erythrocytosis Autosomal Dominant Benign

  • Familial Primary Polycythemia

  • Familial Erythrocytosis, 1

  • Erythrocytosis, Familial, Type 1

Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

T-Cell Acute Lymphoblastic Leukemia
  • T-Cell Leukemia

  • Acute T Cell Leukemia

  • Precursor T Lymphoblastic Leukemia

  • Precursor T-Lymphoblastic Lymphoma/Leukemia

  • T Acute Lymphoblastic Leukemia

  • T-Cell Acute Lymphocytic Leukaemia

  • T-Cell Lymphoblastic Leukemia/Lymphoma

  • Leukemia T-Cell

  • Leukemia, T-Cell

  • Leukemia, Acute, Lymphoblastic, T-Cell

  • Leukemia, T-Cell Acute Lymphoblastic

  • Leukemia, Acute T-Cell

  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

  • Precursor T-Cell Lymphoblastic Lymphoma

  • Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Leukemia, Chronic Myeloid
  • Chronic Myeloid Leukemia

  • Chronic Myelogenous Leukemia

  • CML

  • Chronic Granulocytic Leukemia

  • Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

  • Chronic Myeloid Leukaemia

  • Chronic Granulocytic Leukaemia

  • Chronic Myelogenous Leukaemia

  • Myeloid Leukemia, Chronic

  • Leukemia, Chronic Myelogenous

  • Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

  • Cml - Chronic Myelogenous Leukemia

  • Cgl

  • Chronic Myelocytic Leukemia

  • Leukemia, Chronic Myeloid, Atypical

  • ACML

  • Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

  • Myeloid Leukemia Chronic

  • Leukemia, Myeloid, Chronic

  • Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

  • Cml- [Chronic Myeloid Leukaemia]

  • Cgl - [Chronic Granulocytic Leukaemia]

  • Chronic Myelocytic Leukaemia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus PTPN6 VGNC VGNC:69166
Rattus norvegicus PTPN6 RGD RGD:620660
Mus musculus PTPN6 MGD MGI:96055
Macaca mulatta PTPN6 VGNC VGNC:76607
Bos taurus PTPN6 VGNC VGNC:33541
Canis familiaris PTPN6 VGNC VGNC:45179
Others PTPN6 NCBI