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PTPN11 gene

protein tyrosine phosphatase non-receptor type 11

Key facts

Official symbol
PTPN11
Full name
PTPN11
Chromosome
12
Map location
12q24.13
Organism
Homo sapiens
NCBI Gene ID
5781
Also known as
BPTP3, CFC, JMML, METCDS, NS1, PTP-1D

Function 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].

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Data source: NCBI Gene · alsesAI Gene Library