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Protein-coding gene in the species Homo sapiens

PTPN2

PTPN2
All data from the card 19
Aliases
PTPN2, PTN2, PTPT, TC-PTP, TCELLPTP, TCPTP, protein tyrosine phosphatase, non-receptor type 2, protein tyrosine phosphatase non-receptor type 2
External IDs
OMIM: 176887; MGI: 97806; GeneCards: PTPN2
PDB
Ortholog search: PDBe RCSB
3.1.3.48
↗
Chr.
Chromosome 18 (human)
Band
18p11.21
End
12,929,643 bp
Chr.
Chromosome 18 (mouse)
Band
18|18 E1
End
67,857,665 bp
BioGPS
n/a
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
5771
Ensembl
ENSG00000175354
UniProt
P17706
RefSeq (mRNA)
NM_001207013NM_001308287NM_002828NM_080422NM_080423
RefSeq (protein)
NP_001193942NP_001295216NP_002819NP_536347NP_536348
Location (UCSC)
Chr 18: 12.79 – 12.93 Mb

Tyrosine-protein phosphatase non-receptor type 2 is an enzyme that in humans is encoded by the PTPN2 gene.

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation.

Epidermal growth factor receptor and the adaptor protein Shc were reported to be substrates of this PTP, which suggested the roles in growth factor mediated cell signaling. Three alternatively spliced variants of this gene, which encode isoforms differing at their extreme C-termini, have been described.

The different C-termini are thought to determine the substrate specificity, as well as the cellular localization of the isoforms. Two highly related but distinctly processed pseudogenes that localize to distinct chromosomes have been reported.

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Text from Wikipedia, CC BY-SA 4.0 · Source article