PTPN11 (NM_080601) - protein tyrosine phosphatase non-receptor type 11
Tyrosine-Protein Phosphatase Non-Receptor Type 11 Isoform 2
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PTM Interaction Network Visualisation
Protein 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. [provided by RefSeq, Aug 2016].
Publication Note:
This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Evidence data:
Transcript exon combination :: BC008692.1, SRR1660805.282591.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348]
- Strand
- +
- Chromosome
- 12
- Protein
- 460 residues
- All mutations
- 131
- PTM sites
- 7
- CDS
- 112,856,915 - 112,924,437
- Transcription
- 112,856,535 - 112,924,727
Usage summary
Network
PTM site
Kinases group
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Kinase, PTM site or protein
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