|
|
Gene Symbol |
PTPRC |
|
Aliases |
B220, CD45, CD45R, GP180, L-CA, LCA, LY5, T200 |
|
Entrez Gene ID |
|
|
Gene Name |
Protein tyrosine phosphatase receptor type C |
|
Chromosomal Location |
1q31.3-q32.1 |
|
HGNC ID |
|
|
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, mitosis, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus is classified as a receptor type PTP. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling. Alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jun 2012]
|
|
RefSeq DNA |
|
|
RefSeq mRNA |
|
|
e!Ensembl
Gene |
|
|
Transcript |
ENST00000367379, ENST00000643513, ENST00000348564, ENST00000442510, ENST00000530727, ENST00000645247, ENST00000367367, ENST00000367364, ENST00000413409, ENST00000529828, ENST00000418674, ENST00000573298, ENST00000575923, ENST00000573679, ENST00000576833, ENST00000573477, ENST00000570609, ENST00000571847, ENST00000574441, ENST00000573971, ENST00000574718 |
|
Protein |
ENSP00000356349, ENSP00000494132, ENSP00000306782, ENSP00000411355, ENSP00000433536, ENSP00000494327, ENSP00000356337, ENSP00000356334, ENSP00000405494, ENSP00000469141, ENSP00000393360, ENSP00000458846, ENSP00000461347, ENSP00000458322, ENSP00000458662, ENSP00000461074, ENSP00000458191, ENSP00000458418, ENSP00000482203, ENSP00000461712, ENSP00000483380
|
|
|
Gene Ontology (GO)
GO ID |
Ontology |
Function |
Evidence |
Reference |
GO:0002244 |
Biological process |
Hematopoietic progenitor cell differentiation |
IMP |
21911094 |
GO:0002378 |
Biological process |
Immunoglobulin biosynthetic process |
IMP |
1793833 |
GO:0006469 |
Biological process |
Negative regulation of protein kinase activity |
IBA |
21873635 |
GO:0006469 |
Biological process |
Negative regulation of protein kinase activity |
IDA |
9197241 |
GO:0006470 |
Biological process |
Protein dephosphorylation |
IBA |
21873635 |
GO:0006933 |
Biological process |
Negative regulation of cell adhesion involved in substrate-bound cell migration |
IMP |
21911094 |
GO:0007166 |
Biological process |
Cell surface receptor signaling pathway |
TAS |
2845400 |
GO:0030890 |
Biological process |
Positive regulation of B cell proliferation |
IMP |
1793833 |
GO:0032677 |
Biological process |
Regulation of interleukin-8 production |
IDA |
12100025 |
GO:0042110 |
Biological process |
T cell activation |
TAS |
12354383 |
GO:0044770 |
Biological process |
Cell cycle phase transition |
IMP |
1793833 |
GO:0045860 |
Biological process |
Positive regulation of protein kinase activity |
NAS |
15275963 |
GO:0046425 |
Biological process |
Regulation of JAK-STAT cascade |
IGI |
12574355 |
GO:0048539 |
Biological process |
Bone marrow development |
IMP |
21911094 |
GO:0048864 |
Biological process |
Stem cell development |
IMP |
21911094 |
GO:0050731 |
Biological process |
Positive regulation of peptidyl-tyrosine phosphorylation |
IBA |
21873635 |
GO:0050764 |
Biological process |
Regulation of phagocytosis |
IDA |
12100025 |
GO:0050852 |
Biological process |
T cell receptor signaling pathway |
IDA |
10358156 |
GO:0050852 |
Biological process |
T cell receptor signaling pathway |
TAS |
15557316 |
GO:0061097 |
Biological process |
Regulation of protein tyrosine kinase activity |
IDA |
12100025 |
GO:1903979 |
Biological process |
Negative regulation of microglial cell activation |
TAS |
15095367 |
GO:1904155 |
Biological process |
DN2 thymocyte differentiation |
TAS |
15557316 |
GO:2000473 |
Biological process |
Positive regulation of hematopoietic stem cell migration |
IMP |
21911094 |
GO:2000648 |
Biological process |
Positive regulation of stem cell proliferation |
IMP |
21911094 |
GO:0005886 |
Cellular component |
Plasma membrane |
IDA |
12354383 |
GO:0009897 |
Cellular component |
External side of plasma membrane |
IDA |
17213291 |
GO:0009898 |
Cellular component |
Cytoplasmic side of plasma membrane |
NAS |
15661907 |
GO:0009986 |
Cellular component |
Cell surface |
IDA |
12100025, 12354383, 24337748 |
GO:0016020 |
Cellular component |
Membrane |
HDA |
19946888 |
GO:0016021 |
Cellular component |
Integral component of membrane |
TAS |
15095367 |
GO:0032059 |
Cellular component |
Bleb |
IDA |
12354383 |
GO:0070062 |
Cellular component |
Extracellular exosome |
HDA |
12519789, 20458337 |
GO:0004725 |
Molecular function |
Protein tyrosine phosphatase activity |
IBA |
21873635 |
GO:0004725 |
Molecular function |
Protein tyrosine phosphatase activity |
IDA |
2853967 |
GO:0004725 |
Molecular function |
Protein tyrosine phosphatase activity |
TAS |
15095367 |
GO:0005001 |
Molecular function |
Transmembrane receptor protein tyrosine phosphatase activity |
TAS |
15557316 |
GO:0005515 |
Molecular function |
Protein binding |
IPI |
1970422, 7507203, 8576115, 10369126, 11909961, 12370829, 15946252, 19167335 |
GO:0019901 |
Molecular function |
Protein kinase binding |
IPI |
14625311 |
GO:0030506 |
Molecular function |
Ankyrin binding |
IPI |
12354383 |
GO:0030507 |
Molecular function |
Spectrin binding |
IDA |
12354383 |
GO:0042803 |
Molecular function |
Protein homodimerization activity |
TAS |
12496963 |
|
Protein Information |
|
Protein Name |
Receptor-type tyrosine-protein phosphatase C, CD45 antigen, T200 glycoprotein, T200 leukocyte common antigen, protein tyrosine phosphatase, receptor type, c polypeptide |
|
Function |
Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits and dephosphorylates SKAP1 and FYN. Dephosphorylates LYN, and thereby modulates LYN activity (By similarity). .; (Microbial infection) Acts as a receptor for human cytomegalovirus protein UL11 and mediates binding of UL11 to T-cells, leading to reduced induction of tyrosine phosphorylation of multiple signaling proteins upon T-cell receptor stimulation and impaired T-cell proliferation. |
|
|
|
|
|
UniProt |
|
|
PDB |
|
|
|
|
Interactions |
| |
STRING |
MINT |
IntAct |
ENSP00000260010 |
O60603 |
O60603 |
|
| |
View interactions
|
|
| |
Associated Diseases
Disease group | Disease Name | References |
Digestive System Diseases |
Colitis |
|
Endocrine System Diseases |
PCOS |
|
Eye Diseases |
Retinal Diseases |
|
Immune System Diseases |
Rheumatoid Arthritis |
|
SCID |
|
Neoplasms |
Prostate cancer |
|
Psychiatric/Brain disorders |
Non-organic psychosis |
|
Psychosis |
|
Skin and Connective Tissue Diseases |
Vitiligo |
|
|
References |
|
|
Aydos Alp, Gurel Aykut, Oztemur Islakoglu Yasemin, Noyan Senem, Gokce Bagdagul, Ecemis Tolga, Kaya Cemil, Aksu Arif Tarik, Gur Dedeoglu Bala |
Biotechnology Institute, Ankara University, Ankara, Turkey.| Test Tube Babies Unit, HRS Women Hospital, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey.| Test Tube Babies Unit, Medicana International Ankara Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, Liv Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, TOBB ETU Hospital, Ankara, Turkey.| Department of Gynecology and Obstetrics, HRS Women Hospital, Ankara, Turkey.| Biotechnology Institute, Ankara University, Ankara, Turkey. |
PLoS One. 2016 Dec 20;11(12):e0168875. doi: 10.1371/journal.pone.0168875. |
Abstract
Polycystic ovary syndrome (PCOS) is a metabolic and endocrine disorder which affects women of reproductive age with prevalence of 8-18%. The oocyte within the follicle is surrounded by cumulus cells (CCs), which connect with mural granulosa cells (MGCs) that are responsible for secreting steroid hormones. The main aim of this study is comparing gene expression profiles of MGCs and CCs in PCOS and control samples to identify PCOS-specific differentially expressed genes (DEGs). In this study, two microarray databases were searched for mRNA expression microarray studies performed with CCs and MGCs obtained from PCOS patients and control samples. Three independent studies were selected to be integrated with naive meta-analysis since raw meta-data from these studies were found to be highly correlated. DEGs in these somatic cells were identified for PCOS and control groups. This study enabled us to reveal dysregulation in MAPK (mitogen activated protein kinase), insulin and Wnt signaling pathways between CCs and MGCs in PCOS. The meta-analysis results together with qRT-PCR validations provide evidence that molecular signaling is dysregulated through MGCs and CCs in PCOS, which is important for follicle and oocyte maturation and may contribute to the pathogenesis of the syndrome. |
|
|
|
|
| © 2019, Biomedical Informatics Centre, NIRRH |
National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400 012
Tel: 91-22-24192104, Fax No: 91-22-24139412
|