FB2025_02 , released April 17, 2025
Gene: Dmel\Pten
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General Information
Symbol
Dmel\Pten
Species
D. melanogaster
Name
Phosphatase and tensin homolog
Annotation Symbol
CG5671
Feature Type
FlyBase ID
FBgn0026379
Gene Model Status
Stock Availability
Enzyme Name (EC)
protein-serine/threonine phosphatase (3.1.3.16)
protein-tyrosine-phosphatase (3.1.3.48)
phosphatidylinositol-3-phosphatase (3.1.3.64)
phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase (3.1.3.67)
Gene Summary
Phosphatase and tensin homolog (Pten) encodes a dual lipid and protein phosphatase that primarily counters the effects of the insulin-regulated lipid kinase, encoded by Pi3K92E. It inhibits cell growth, cell proliferation and cellular events controlling cytoskeletal and junctional rearrangements. [Date last reviewed: 2018-10-18] (FlyBase Gene Snapshot)
Also Known As

dPTEN

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
2-40
RefSeq locus
NT_033779 REGION:10256319..10261049
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (68 terms)
Molecular Function (10 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (10 terms)
CV Term
Evidence
References
inferred from electronic annotation with InterPro:IPR017361
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from electronic annotation with InterPro:IPR045101
inferred from electronic annotation with InterPro:IPR017361
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from biological aspect of ancestor with PANTHER:PTN000266847
inferred from electronic annotation with InterPro:IPR017361
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from biological aspect of ancestor with PANTHER:PTN000959472
Biological Process (52 terms)
Terms Based on Experimental Evidence (44 terms)
CV Term
Evidence
References
inferred from mutant phenotype
involved_in autophagy
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in larval development
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:Atg18a; FB:FBgn0035850
inferred from genetic interaction with FLYBASE:Atg1; FB:FBgn0260945
involved_in lipid homeostasis
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in metamorphosis
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
Terms Based on Predictions or Assertions (10 terms)
CV Term
Evidence
References
involved_in cell motility
inferred from biological aspect of ancestor with PANTHER:PTN000959472
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from electronic annotation with InterPro:IPR017361
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from biological aspect of ancestor with PANTHER:PTN000959472
inferred from electronic annotation with InterPro:IPR017361
inferred from sequence or structural similarity with UniProtKB:P60484
inferred from sequence or structural similarity with UniProtKB:P60484
Cellular Component (6 terms)
Terms Based on Experimental Evidence (1 term)
CV Term
Evidence
References
inferred from mutant phenotype
Terms Based on Predictions or Assertions (5 terms)
CV Term
Evidence
References
is_active_in cell projection
inferred from biological aspect of ancestor with PANTHER:PTN000959472
located_in cytoplasm
inferred from sequence or structural similarity with UniProtKB:P60484
is_active_in cytosol
inferred from biological aspect of ancestor with PANTHER:PTN000266847
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN000959472
located_in nucleus
inferred from sequence or structural similarity with UniProtKB:P60484
is_active_in plasma membrane
inferred from biological aspect of ancestor with PANTHER:PTN000959472
Protein Family (UniProt)
-
Catalytic Activity (EC/Rhea)
protein tyrosine phosphatase activity
O-phospho-L-tyrosyl-[protein] + H2O = L-tyrosyl-[protein] + phosphate (3.1.3.48)
RHEA 10684: phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase activity
a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4,5-trisphosphate) + H2O = a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-4,5- bisphosphate) + phosphate (3.1.3.67)
RHEA 25017: protein serine/threonine phosphatase activity
(1) O-phospho-L-seryl-[protein] + H2O = L-seryl-[protein] + phosphate (3.1.3.16)
(2) O-phospho-L-threonyl-[protein] + H2O = L-threonyl-[protein] + phosphate (3.1.3.16)
phosphatidylinositol-3-phosphate phosphatase activity
a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-3-phosphate) + H2O = a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol) + phosphate (3.1.3.64)
RHEA 12316: inositol-1,3,4,5-tetrakisphosphate 3-phosphatase activity
RHEA 77155:
Summaries
Gene Snapshot
Phosphatase and tensin homolog (Pten) encodes a dual lipid and protein phosphatase that primarily counters the effects of the insulin-regulated lipid kinase, encoded by Pi3K92E. It inhibits cell growth, cell proliferation and cellular events controlling cytoskeletal and junctional rearrangements. [Date last reviewed: 2018-10-18]
Gene Group (FlyBase)
DUAL SPECIFICITY PROTEIN PHOSPHATASES -
Dual Specificity Phosphatases (DSP) can dephosphorylate both tyrosine and serine/threonine residues. Additionally, DSPs may target a much larger and diverse set of substrates, including phosphoinositide lipids, RNA 5'-triphosphate and carbohydrates. (Adapted from FBrf0227974).
PHOSPHATIDYLINOSITOL PHOSPHATE AND INOSITOL PHOSPHATE PHOSPHATASES -
Phosphoinositide phosphate (PtdInsP) phosphatases and Inositol phosphate (InsP) phosphatases are enzymes that catalyze the hydrolysis of phosphate groups from inositol. Many of these phosphatases can act on both PtdInsP and InsP substrates. (Adapted from PMID:23681533).
Negative Regulators of Insulin-like Receptor Signaling Pathway -
Negative regulators of the Insulin-like Receptor signaling pathway suppress Insulin-like receptor (InR) activation or the activity of intracellular effectors. (Adapted from FBrf0232297, FBrf0230017 and FBrf0229989).
Negative Regulators of EGFR Signaling Pathway -
Negative regulators of Epidermal Growth Factor Receptor signaling down-regulate the pathway, suppressing the activation of ERK kinase (rl) or acting on downstream effectors.
Summary (Interactive Fly)

lipid and protein phosphatase acting in insulin pathway - PTEN, a tumour suppressor, is a lipid and protein phosphatase that inhibits phosphoinositide 3-kinase (PI3K)-dependent signalling by dephosphorylating phosphatidylinositol 3,4,5-trisphosphate

Gene Model and Products
Number of Transcripts
7
Number of Unique Polypeptides
3

Please see the JBrowse view of Dmel\Pten for information on other features

To submit a correction to a gene model please use the Contact FlyBase form

Protein Domains (via Pfam)
Isoform displayed:
Pfam protein domains
InterPro name
classification
start
end
Protein Domains (via SMART)
Isoform displayed:
SMART protein domains
InterPro name
classification
start
end
Structure
Protein 3D structure   (Predicted by AlphaFold)   (AlphaFold entry Q7KMQ6)

If you don't see a structure in the viewer, refresh your browser.
Model Confidence:
  • Very high (pLDDT > 90)
  • Confident (90 > pLDDT > 70)
  • Low (70 > pLDDT > 50)
  • Very low (pLDDT < 50)

AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.

Experimentally Determined Structures
Crossreferences
Comments on Gene Model

Alternative translation stop created by use of multiphasic reading frames within coding region.

Annotated transcripts do not represent all supported alternative splices within 5' UTR.

Gene model reviewed during 5.46

Low-frequency RNA-Seq exon junction(s) not annotated (in 3' UTR).

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0089905
2568
509
FBtr0089904
2355
514
FBtr0089902
1803
418
FBtr0089900
2125
514
FBtr0089901
2338
509
FBtr0300562
2617
514
FBtr0301521
2467
514
Additional Transcript Data and Comments
Reported size (kB)

1.872 (longest cDNA)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0088844
58.4
509
7.25
FBpp0088843
59.0
514
7.25
FBpp0088841
48.1
418
7.23
FBpp0088839
59.0
514
7.25
FBpp0088840
58.4
509
7.25
FBpp0289789
59.0
514
7.25
FBpp0290736
59.0
514
7.25
Polypeptides with Identical Sequences

The group(s) of polypeptides indicated below share identical sequence to each other.

514 aa isoforms: Pten-PB, Pten-PD, Pten-PG, Pten-PH
509 aa isoforms: Pten-PA, Pten-PE
Additional Polypeptide Data and Comments
Reported size (kDa)

514, 509 (aa)

511, 509, 418 (aa)

Comments
External Data
Linkouts
Sequences Consistent with the Gene Model
Mapped Features

Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Pten using the Feature Mapper tool.

External Data
Crossreferences
Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
Linkouts
Expression Data
Testis-specificity index

The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).

-1.13

Transcript Expression
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
organism

Comment: maternally deposited

Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
mass spectroscopy
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data
Marker for
 
Subcellular Localization
CV Term
Evidence
References
inferred from mutant phenotype
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\Pten in JBrowse
RNA-Seq by Region - Search RNA-Seq expression levels by exon or genomic region
Reference
See Gelbart and Emmert, 2013 for analysis details and data files for all genes.
Developmental Proteome: Life Cycle
Developmental Proteome: Embryogenesis
External Data and Images
Linkouts
BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Flygut - An atlas of the Drosophila adult midgut
Images
FlyExpress - Embryonic expression images (BDGP data)
  • Stages(s) 1-3
  • Stages(s) 4-6
  • Stages(s) 9-10
  • Stages(s) 11-12
  • Stages(s) 13-16
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 18 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 36 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of Pten
Transgenic constructs containing regulatory region of Pten
Aberrations (Deficiencies and Duplications) ( 5 )
Variants
Variant Molecular Consequences
Alleles Representing Disease-Implicated Variants
Phenotypes
For more details about a specific phenotype click on the relevant allele symbol.
Lethality
Allele
Sterility
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
lipid droplet & larval oenocyte, with Scer\GAL4ppl.PP
lipid particle & nurse cell | somatic clone
nurse cell & actin cytoskeleton | germ-line clone
nurse cell & nucleus | germ-line clone
wing & cell | somatic clone
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (25)
13 of 14
Yes
Yes
 
103  
6 of 14
No
Yes
6 of 14
No
Yes
2 of 14
No
No
1  
2 of 14
No
No
2  
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
3  
1 of 14
No
No
2  
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
3  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
6  
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (21)
13 of 14
Yes
Yes
6 of 14
No
Yes
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (19)
13 of 14
Yes
Yes
6 of 14
No
Yes
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (11)
10 of 13
Yes
Yes
3 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
Yes
1 of 13
No
No
Danio rerio (Zebrafish) (26)
12 of 14
Yes
Yes
11 of 14
No
Yes
5 of 14
No
Yes
2 of 14
No
No
2 of 14
No
No
2 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
Caenorhabditis elegans (Nematode, roundworm) (16)
8 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
Anopheles gambiae (African malaria mosquito) (11)
6 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (11)
8 of 13
Yes
Yes
8 of 13
Yes
Yes
7 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Saccharomyces cerevisiae (Brewer's yeast) (2)
9 of 13
Yes
Yes
1 of 13
No
No
Schizosaccharomyces pombe (Fission yeast) (2)
8 of 12
Yes
Yes
1 of 12
No
No
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:Pten. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (7)
2 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
Human Disease Associations
FlyBase Human Disease Model Reports
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 9 )
Potential Models Based on Orthology ( 3 )
Modifiers Based on Experimental Evidence ( 4 )
Allele
Disease
Interaction
References
Disease Associations of Human Orthologs (via DIOPT v9.1 and OMIM)
Note that ortholog calls supported by only 1 or 2 algorithms (DIOPT score < 3) are not shown.
Functional Complementation Data
Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature.
Dmel gene
Ortholog showing functional complementation
Supporting References
Interactions
Summary of Physical Interactions
Interaction Browsers

Please see the Physical Interaction reports below for full details
protein-protein
Physical Interaction
Assay
References
Summary of Genetic Interactions
Interaction Browsers

Please look at the allele data for full details of the genetic interactions
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
External Data
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
MIST (genetic) - An integrated Molecular Interaction Database
MIST (protein-protein) - An integrated Molecular Interaction Database
Pathways
Signaling Pathways (FlyBase)
Metabolic Pathways
FlyBase
External Links
KEGG Metabolic Pathways - A collection of manually drawn metabolic pathway maps representing knowledge of molecular interaction, reaction and relation networks.
Reactome Metabolic Pathways - An open-source, open access, manually curated and peer-reviewed metabolic pathway database.
External Data
Linkouts
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
2L
Recombination map
2-40
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
31B1-31B1
Limits computationally determined from genome sequence between P{lacW}me31Bk06607 and P{PZ}nmd08774
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
31A1-31D6
31B-31C
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (24)
Genomic Clones (26)
cDNA Clones (27)
 

Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.

cDNA clones, fully sequenced
BDGP DGC clones
Other clones
Drosophila Genomics Resource Center cDNA clones

For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.

cDNA Clones, End Sequenced (ESTs)
BDGP DGC clones
RNAi and Array Information
Linkouts
DRSC - Results frm RNAi screens
Antibody Information
Laboratory Generated Antibodies
Commercially Available Antibodies
 
Cell Line Information
Publicly Available Cell Lines
Other Stable Cell Lines
 
    Other Comments

    dsRNA has been made from templates generated with primers directed against this gene.

    dsRNA made from templates generated with primers directed against this gene results in an increase in mean cell diameter.

    dsRNA made from templates generated with primers directed against this gene used to treat S2 cells.

    dsRNA made from templates generated with primers directed against this gene increase the levels of phosphorylation of boh Akt1 and S6k in S2 cells.

    One of 42 Drosophila genes identified as being most likely to reveal molecular and cellular mechanisms of nervous system development or plasticity relevant to human Mental Retardation disorders.

    PI3K activity is regulated through EcR signalling in a cell-autonomous manner to allow programmed autophagy in the fat body.

    dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.

    RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in Kc167 cells: change from round to spindle-shaped, with the formation of F-actin puncta and microtubule extensions. Alterations of cell shape are also evident in S2R+ cells - they become round and detached. The Kc167 cell-shape change is suppressed by simultaneous treatment with dsRNA targetted against Akt1, CG31187, LIMK1, MAPk-Ak2, Pi3K92E, slpr or wee.

    Pten plays an essential role in the control of, cell size, cell number, and organ size.

    Pten acts antagonistically to Pi3K92E and chico. In direction of increasing cytology: chico- bsk- Ror+ Pten-

    Pten has a complex role in regulating tissue and body size. Pten regulates the subcellular organization of the actin cytoskeleton in multiple cell types.

    Both inactivation and overexpression of Pten affect cell size, and overexpression of Pten inhibits cell cycle progression at early mitosis and promotes cell death during eye development. Phenotypes caused by overexpression of Hsap\PTEN and Pten are indistinguishable.

    The phosphatase activity of Pten is necessary for it to exert its functions during development. In direction of increasing cytology: Rsf1+ Pten+ CG5676+ Ror- bsk+ chico+

    Pten acts in the insulin signalling pathway. All signals from the InR protein can be antagonized by Pten.

    Pten regulates cell size and cell proliferation via the actin cytoskeleton.

    Relationship to Other Genes
    Source for database merge of

    Source for merge of: Pten CG5671

    Additional comments
    Nomenclature History
    Source for database identify of
    Nomenclature comments
    Etymology
    Synonyms and Secondary IDs (18)
    Reported As
    Symbol Synonym
    PTEN
    (Reimels et al., 2024, Banach-Latapy et al., 2023, Frappaolo and Giansanti, 2023, Ikawa et al., 2023, Koehler and Huber, 2023, Krejčová et al., 2023, Buckley and St Johnston, 2022, Jarabo et al., 2022, Noguchi et al., 2022, Nogueira Alves et al., 2022, Alvarez-Ochoa et al., 2021, Gautam et al., 2021, Lam Wong and Verheyen, 2021, Yu and Hyun, 2021, Barretto et al., 2020, Coelho, 2020, Jossin, 2020, Luo et al., 2020, Rambur et al., 2020, Sudhakar et al., 2020, Yuan et al., 2020, Borreguero-Muñoz et al., 2019, Galenza and Foley, 2019, Hwang et al., 2019, Lang et al., 2019, Mondin et al., 2019, Rosen et al., 2019, Shadkhoo and Mani, 2019, Ahmad et al., 2018, Ghiglione et al., 2018, Gruntenko and Rauschenbach, 2018, Inoue et al., 2018, Muñoz-Soriano et al., 2018, Parvy et al., 2018, Pichaud, 2018, Poon et al., 2018, Richardson and Portela, 2018, Spéder and Brand, 2018, Swevers et al., 2018, Brace and DiAntonio, 2017, Misra et al., 2017, Moeller et al., 2017, Murillo-Maldonado and Riesgo-Escovar, 2017, Paglia et al., 2017, Romero-Pozuelo et al., 2017, Chang et al., 2016, Cheng et al., 2016, Hemalatha et al., 2016, Kaynar et al., 2016, Marmor-Kollet and Schuldiner, 2016, Yadav et al., 2016, Aradhya et al., 2015, Bennett et al., 2015, Nässel et al., 2015, Devergne et al., 2014, Oliveira et al., 2014, Pichaud, 2014, Radermacher et al., 2014, Wang et al., 2014, Andersen et al., 2013, Chen and Zhang, 2013, Hwang et al., 2013, Koyama et al., 2013, Nowak et al., 2013, Okamoto et al., 2013, Oortveld et al., 2013, Shim et al., 2013, Sim and Denlinger, 2013, Tran et al., 2013, Wong et al., 2013, Yin et al., 2013, Chountala et al., 2012, Dahlgaard et al., 2012, Denton et al., 2012, Eleftherianos and Castillo, 2012, Gault et al., 2012, Lv et al., 2012, Ogmundsdóttir et al., 2012, Tepass, 2012, Bangi et al., 2011, Friedman et al., 2011, Laprise and Tepass, 2011, Miles et al., 2011, Nakajima et al., 2011, Oldham, 2011, Park et al., 2011, Partridge et al., 2011, Poon et al., 2011, Read, 2011, Resnik-Docampo and de Celis, 2011, Tang et al., 2011, Yang and Xu, 2011, Delanoue et al., 2010, Lee et al., 2010, Mesquita et al., 2010, Montagne et al., 2010, Tsuda et al., 2010, Tsuda et al., 2010, Géminard et al., 2009, Ikeya et al., 2009, Ninov et al., 2009, Nuzhdin et al., 2009, Read et al., 2009, Shelly et al., 2009, Werz et al., 2009, Bakal et al., 2008, Honegger et al., 2008, Howlett et al., 2008, Lee et al., 2008, Mattila et al., 2008, Rafel and Milán, 2008, Seisenbacher et al., 2008, Vereshchagina et al., 2008, Basu and Krek, 2007, Bergman et al., 2007, Cortina-Andrada et al., 2007, Gutierrez et al., 2007, Hall et al., 2007, Hietakangas and Cohen, 2007, Hoshizaki and Gibbs, 2007, Jovceva et al., 2007, Juhász et al., 2007, Libert, 2007, Palmer and Pichaud, 2007, Tyler et al., 2007, Wilson et al., 2007, Betschinger et al., 2006, Edgar, 2006, Edgar, 2006, Fehon, 2006, Frias et al., 2006, Frias et al., 2006, Guertin et al., 2006, Lindmo et al., 2006, Pinal et al., 2006, Shiojima and Walsh, 2006, Vereshchagina and Wilson, 2006, Cygnar et al., 2005, McNeill and Bateman, 2005, Mikeladze-Dvali et al., 2005, Mirth et al., 2005, Shingleton, 2005, Bilder, 2004, Clague et al., 2004, Pan et al., 2004, Scott et al., 2004, Scott et al., 2004, von Stein et al., 2004, Hardie, 2003, von Stein et al., 2003, Gao et al., 2002, Neufeld, 2001.1.11, Oldham et al., 2001, Potter et al., 2000, Scanga et al., 2000, Weinkove and Leevers, 2000, Wilson et al., 2000, Smith, 1999.6.23, Smith, 1999.6.23, Smith, 1999.6.23)
    Pten
    (Sánchez-Sánchez et al., 2025, Barbaste et al., 2023, Hou et al., 2023, Dalton et al., 2022, Ecovoiu et al., 2022, Li et al., 2022, Lu et al., 2022, Raghu, 2022.1.6, Zhou et al., 2022, Zipper et al., 2022, Anqueira-González et al., 2021, Aromolaran et al., 2021, Azuma et al., 2021, Bilder et al., 2021, García-López et al., 2021, Gong et al., 2021, Han et al., 2021, Kim and O'Connor, 2021, Liguori et al., 2021, Ostalé et al., 2021, Parkhitko et al., 2021, Salim et al., 2021, Yuen et al., 2021, Zhou et al., 2021, Allen et al., 2020, Cui et al., 2020, Gangwani et al., 2020, Gupta and Stocker, 2020, Luo et al., 2020, Morata and Calleja, 2020, Parniewska and Stocker, 2020, Singh et al., 2020, Strilbytska et al., 2020, Sun et al., 2020, Vega-Cuesta et al., 2020, Yusuff et al., 2020, Zeng et al., 2020, Birnbaum et al., 2019, Brodskiy et al., 2019, Chen and Read, 2019, Fahey-Lozano et al., 2019, Hall et al., 2019, Hunt et al., 2019, Hwang et al., 2019, Lattner et al., 2019, Luhur et al., 2019, Pfeifle et al., 2019, Zheng, 2019.3.1, Ayala et al., 2018, Kang et al., 2018, Nowak et al., 2018, Tang et al., 2018, Villegas et al., 2018, Viswanatha et al., 2018, Wang et al., 2018, Fedina et al., 2017, Hevia et al., 2017, Mensah et al., 2017, Song et al., 2017, Transgenic RNAi Project members, 2017-, Di Cara and King-Jones, 2016, Padash Barmchi et al., 2016, Pan et al., 2016, Schmid et al., 2016, Vinayagam et al., 2016, Xu et al., 2016, Grotewiel and Bettinger, 2015, Hatzihristidis et al., 2015, Jia et al., 2015, Kwon et al., 2015, Mensah et al., 2015, Park et al., 2015, Song et al., 2015, Sopko et al., 2015, Tokusumi et al., 2015, Das et al., 2014, Khadilkar et al., 2014, Sato-Miyata et al., 2014, Sopko et al., 2014, Wang et al., 2014, Carter, 2013, Dobens and Dobens, 2013, Heigwer et al., 2013, Pickering et al., 2013, Pomerantz and Blau, 2013, Rousso et al., 2013, Schertel et al., 2013, Sopko and Perrimon, 2013, Tixier et al., 2013, Tixier et al., 2013, Howell et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Justiniano et al., 2012, Kuo et al., 2012, Marinari et al., 2012, Papatheodorou et al., 2012, Pircs et al., 2012, Song et al., 2012, Tokusumi et al., 2012, Zhai et al., 2012, Djiane et al., 2011, Eddison et al., 2011, Lindquist et al., 2011, Sousa-Nunes et al., 2011, Willecke et al., 2011, Demontis and Perrimon, 2010, Haberman et al., 2010, Kim et al., 2010, Lee et al., 2010, Nedelsky et al., 2010, Sinenko et al., 2010, Zheng and Sehgal, 2010, Alvarez-Ponce et al., 2009, Demontis and Perrimon, 2009, Doumanis et al., 2009, Mirth et al., 2009, Mummery-Widmer et al., 2009, Parrish et al., 2009, Qian and Bodmer, 2009, Rhiner et al., 2009, Sims et al., 2009, Hou et al., 2008, Yin et al., 2008, Zhou et al., 2008, Chen et al., 2007, Ford et al., 2007, Knox et al., 2007, Friedman and Perrimon, 2006, Wiggin et al., 2005, Bruckner et al., 2004, Wheeler et al., 2004)
    Name Synonyms
    Drosophila phosphatase and tensin homologue deleted on chromosome 10
    PI 3-phosphatase
    Phosphatase and tensin homolog
    Phosphatase and tensin homologue
    PtdIns(3,4,5)P3 phosphatase
    phosphatase and tensin homolog
    phosphatidylinositol (3,4,5)-trisphosphate phosphatase
    Secondary FlyBase IDs
    • FBgn0032201
    Datasets (0)
    Study focus (0)
    Experimental Role
    Project
    Project Type
    Title
    Study result (0)
    Result
    Result Type
    Title
    External Crossreferences and Linkouts ( 103 )
    Sequence Crossreferences
    NCBI Gene - Gene integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources worldwide.
    GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
    GenBank Protein - A collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB.
    RefSeq - A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.
    UniProt/GCRP - The gene-centric reference proteome (GCRP) provides a 1:1 mapping between genes and UniProt accessions in which a single 'canonical' isoform represents the product(s) of each protein-coding gene.
    UniProt/TrEMBL - Automatically annotated and unreviewed records of protein sequence and functional information
    Other crossreferences
    AlphaFold DB - AlphaFold provides open access to protein structure predictions for the human proteome and other key proteins of interest, to accelerate scientific research.
    BDGP expression data - Patterns of gene expression in Drosophila embryogenesis
    DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
    EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
    FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
    FlyMine - An integrated database for Drosophila genomics
    KEGG Genes - Molecular building blocks of life in the genomic space.
    MARRVEL_MODEL - MARRVEL (model organism gene)
    Linkouts
    BioGRID - A database of protein and genetic interactions.
    Drosophila Genomics Resource Center - Drosophila Genomics Resource Center (DGRC) cDNA clones
    DroID - A comprehensive database of gene and protein interactions.
    DRSC - Results frm RNAi screens
    Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
    FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
    FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
    Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
    Flygut - An atlas of the Drosophila adult midgut
    iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
    Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
    KEGG Metabolic Pathways - A collection of manually drawn metabolic pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    MIST (genetic) - An integrated Molecular Interaction Database
    MIST (protein-protein) - An integrated Molecular Interaction Database
    Reactome Metabolic Pathways - An open-source, open access, manually curated and peer-reviewed metabolic pathway database.
    SignaLink - A signaling pathway resource with multi-layered regulatory networks.
    References (563)