Homo sapiens Protein: PTPN14 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-106647.5 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | PTPN14 | ||||||||||||||||||
Protein Name | protein tyrosine phosphatase, non-receptor type 14 | ||||||||||||||||||
Synonyms | PEZ; PTP36; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000355923 | ||||||||||||||||||
InnateDB Gene | IDBG-106645 (PTPN14) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Protein tyrosine phosphatase which may play a role in the regulation of lymphangiogenesis, cell-cell adhesion, cell- matrix adhesion, cell migration, cell growth and also regulates TGF-beta gene expression, thereby modulating epithelial- mesenchymal transition. Mediates beta-catenin dephosphorylation at adhesion junctions. Acts as a negative regulator of the oncogenic property of YAP, a downstream target of the hippo pathway, in a cell density-dependent manner. May function as a tumor suppressor. {ECO:0000269PubMed:10934049, ECO:0000269PubMed:12808048, ECO:0000269PubMed:17893246, ECO:0000269PubMed:20826270, ECO:0000269PubMed:22233626, ECO:0000269PubMed:22525271, ECO:0000269PubMed:22948661}. | ||||||||||||||||||
Subcellular Localization | Cytoplasm. Cytoplasm, cytoskeleton {ECO:0000250}. Nucleus. Note=Translocation into the nucleus is associated with induction of cell proliferation. Partially colocalized with actin filaments at the plasma membrane. | ||||||||||||||||||
Disease Associations | Choanal atresia and lymphedema (CHATLY) [MIM:613611]: A disease characterized by posterior choanal atresia and lymphedema. Additional features are a high-arched palate, hypoplastic nipples, and mild pectus excavatum. {ECO:0000269PubMed:20826270}. Note=The disease is caused by mutations affecting the gene represented in this entry. A homozygous deletion in PTPN14 predicted to result in frameshift and premature truncation, has been shown to be the cause of choanal atresia and lymphedema in one family.Note=Influence clinical severity of hereditary haemorragic telagiectasia (HHT).Note=Frequently mutated in a variety of human cancers. | ||||||||||||||||||
Tissue Specificity | Ubiquitous. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 42 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000242
Protein-tyrosine phosphatase, receptor/non-receptor type IPR000299 FERM domain IPR000340 Dual specificity phosphatase, catalytic domain IPR000387 Protein-tyrosine/Dual specificity phosphatase IPR003595 Protein-tyrosine phosphatase, catalytic IPR014392 Protein-tyrosine phosphatase, non-receptor type-14, -21 IPR018979 FERM, N-terminal IPR018980 FERM, C-terminal PH-like domain IPR019748 FERM central domain IPR019749 Band 4.1 domain IPR019750 Band 4.1 family IPR029021 Protein-tyrosine phosphatase-like IPR029071 Ubiquitin-related domain |
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PFAM |
PF00102
PF00782 PF09379 PF09380 PF00373 |
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PRINTS |
PR00700
PR00935 |
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PIRSF |
PIRSF000934
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SMART |
SM00194
SM00404 SM00295 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q15678 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q15678 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 5784 | ||||||||||||||||||
UniGene | Hs.688910 | ||||||||||||||||||
RefSeq | NP_005392 | ||||||||||||||||||
HUGO | HGNC:9647 | ||||||||||||||||||
OMIM | 603155 | ||||||||||||||||||
CCDS | CCDS1514 | ||||||||||||||||||
HPRD | 04402 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AL445305 AL592216 AL603838 AL929236 BC101754 BC104803 CH471100 X82676 | ||||||||||||||||||
GenPept | AAI01755 AAI04804 CAA57993 CAH70919 CAH72982 CAH73027 CAH73479 EAW93351 | ||||||||||||||||||