PTPN11

GENERAL INFORMATION

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Gene name

PTPN11

Gene description

Protein tyrosine phosphatase, non-receptor type 11

Protein class

Cancer-related genes
Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
RAS pathway related proteins

Predicted localization

Intracellular

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
CAB005377
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

PTPN11 (HGNC Symbol)

Synonyms

BPTP3, NS1, PTP2C, SH-PTP2, SHP-2, SHP2

Description

Protein tyrosine phosphatase, non-receptor type 11 (HGNC Symbol)

Entrez gene 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. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

Chromosome

12

Cytoband

q24.13

Chromosome location (bp)

112418351 - 112509913

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000179295 (version 78.38)

Entrez gene

5781

UniProt

Q06124 (UniProt - Evidence at protein level)

neXtProt

NX_Q06124

Antibodypedia

PTPN11 antibodies


PROTEIN BROWSER

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ENST00000351677
 
ENST00000392597
 
ENST00000530818
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

PTPN11-001 ENSP00000340944
ENST00000351677
Q06124
Show all »
Show » Show » 593 68 No 0
PTPN11-002 ENSP00000376376
ENST00000392597
Q06124
Show all »
Show » Show » 460 52.8 No 0
PTPN11-004 ENSP00000437013
ENST00000530818
Show » 108 12.2 No 0