FB2025_05 , released December 11, 2025
Gene: Dmel\Imp
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General Information
Symbol
Dmel\Imp
Species
D. melanogaster
Name
IGF-II mRNA-binding protein
Annotation Symbol
CG1691
Feature Type
FlyBase ID
FBgn0285926
Gene Model Status
Stock Availability
Gene Summary
IGF-II mRNA-binding protein (Imp) encodes a protein that regulates the stability, translation and/or transport of its associated mRNAs, a large number of them encoding F-actin regulators. It is an essential protein required for neural and germline stem cell maturation, neuronal remodeling, as well as the expression modulation of asymmetrically localized maternal mRNAs. [Date last reviewed: 2019-03-07] (FlyBase Gene Snapshot)
Also Known As

MRE11, dIMP, l(1)G0072, FGC026A04, KH-domain protein

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
1-33
RefSeq locus
NC_004354 REGION:10787869..10824277
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (23 terms)
Molecular Function (4 terms)
Terms Based on Experimental Evidence (2 terms)
CV Term
Evidence
References
inferred from direct assay
Terms Based on Predictions or Assertions (3 terms)
CV Term
Evidence
References
inferred from biological aspect of ancestor with PANTHER:PTN000815570
inferred from electronic annotation with InterPro:IPR004087
inferred from electronic annotation with InterPro:IPR004087, InterPro:IPR035979
Biological Process (12 terms)
Terms Based on Experimental Evidence (9 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
involved_in neuron remodeling
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in spermatogenesis
inferred from expression pattern
inferred from mutant phenotype
Terms Based on Predictions or Assertions (3 terms)
CV Term
Evidence
References
inferred from biological aspect of ancestor with PANTHER:PTN000815570
inferred from biological aspect of ancestor with PANTHER:PTN000815570
Cellular Component (7 terms)
Terms Based on Experimental Evidence (6 terms)
CV Term
Evidence
References
located_in axon
inferred from direct assay
inferred from high throughput direct assay
located_in cytoplasm
inferred from high throughput direct assay
located_in cytosol
inferred from direct assay
inferred from direct assay
inferred from high throughput direct assay
Terms Based on Predictions or Assertions (3 terms)
CV Term
Evidence
References
is_active_in cytoplasm
inferred from biological aspect of ancestor with PANTHER:PTN000032600
is_active_in cytosol
inferred from biological aspect of ancestor with PANTHER:PTN000815570
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN000032600
Gene Group (FlyBase)
Protein Family (UniProt)
-
Summaries
Gene Snapshot
IGF-II mRNA-binding protein (Imp) encodes a protein that regulates the stability, translation and/or transport of its associated mRNAs, a large number of them encoding F-actin regulators. It is an essential protein required for neural and germline stem cell maturation, neuronal remodeling, as well as the expression modulation of asymmetrically localized maternal mRNAs. [Date last reviewed: 2019-03-07]
Pathway (FlyBase)
POSITIVE REGULATORS OF JAK-STAT SIGNALING PATHWAY -
Positive regulators of JAK-STAT signaling up-regulate the pathway, enhancing transcriptional control by Stat92E.
POSITIVE REGULATORS OF NOTCH SIGNALING PATHWAY -
The Notch receptor signaling pathway is activated by the binding of the transmembrane receptor Notch (N) to transmembrane ligands, Dl or Ser, presented on adjacent cells. This results in the proteolytic cleavage of N, releasing the intracellular domain (NICD). NICD translocates into the nucleus, interacting with Su(H) and mam to form a transcription complex, which up-regulates transcription of Notch-responsive genes. Positive regulators of the pathway enhance the signal from the sending cell or the response in the receiving cell. (Adapted from FBrf0225731 and FBrf0192604).
Summary (Interactive Fly)

zipcode-binding protein - regulator of RNA transport in oocytes and neurons - regulates aging of the Drosophila testis stem-cell niche - contributes to the localized expression of gurken mRNA in the oocyte - counteracts endogenous small interfering RNAs to stabilize mRNAs

Gene Model and Products
Number of Transcripts
12
Number of Unique Polypeptides
5

Please see the JBrowse view of Dmel\Imp 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 M9NF14)

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

Gene model reviewed during 5.55

Gene model reviewed during 5.46

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

Low-frequency RNA-Seq exon junction(s) not annotated.

Stage-specific extension of 3' UTRs observed during embryogenesis (FBrf0215804); all variants may not be annotated.

Tissue-specific extension of 3' UTRs observed during later stages (FBrf0218523, FBrf0219848); all variants may not be annotated

Gene model reviewed during 5.56

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0073420
3300
566
FBtr0073419
2863
566
FBtr0073418
6762
566
FBtr0073416
8752
573
FBtr0073417
3711
573
FBtr0073413
4481
573
FBtr0073415
5684
573
FBtr0073414
12045
573
FBtr0301409
3942
580
FBtr0305149
3468
631
FBtr0305150
4220
638
FBtr0346315
3824
638
Additional Transcript Data and Comments
Reported size (kB)
Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0073276
62.1
566
10.16
FBpp0073275
62.1
566
10.16
FBpp0073274
62.1
566
10.16
FBpp0073272
62.7
573
9.32
FBpp0073273
62.7
573
9.32
FBpp0073269
62.7
573
9.32
FBpp0073271
62.7
573
9.32
FBpp0073270
62.7
573
9.32
FBpp0290623
63.4
580
8.77
FBpp0293679
69.4
631
9.72
FBpp0293680
69.9
638
8.29
FBpp0312047
69.9
638
8.29
Polypeptides with Identical Sequences

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

573 aa isoforms: Imp-PD, Imp-PE, Imp-PF, Imp-PG, Imp-PH
566 aa isoforms: Imp-PA, Imp-PB, Imp-PC
638 aa isoforms: Imp-PL, Imp-PM
Additional Polypeptide Data and Comments
Reported size (kDa)
Comments
External Data
Linkouts
Sequences Consistent with the Gene Model
Nucleotide / Polypeptide Records
 
Mapped Features

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

External Data
Crossreferences
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).

0.01

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

Comment: 4 diffuse circumferential stripes that broaded with time

organism

Comment: extended 3' UTR isoform

Additional Descriptive Data

Imp transcripts are detected early and late in embryogenesis but transcripts containing the 3' UTR extension (~8.5 kb) are only detected at later stages and appear after the maternal-to-zygotic transition. The 3' UTR extension isoforms are highly enriched in nervous system tissues.

Imp expression at embryonic stages 1-4 is localized to the posterior pole of the embryo.

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

Immunolocalization shows that Imp is expressed in the -- and pole cells in blastoderm embryos and in the ventral nerve cord in stage 14-16 embryos. Double staining with an antibody to futsch reveals that Imp is expressed in peripheral sensory neurons and some futsch-negative cells surrounding them. Overlap with pros expression reveals Imp expression in the scolopale cells of chordotonal organs and in sheath cells of the external sensory organs. No staining was observed in peripheral motor axons or in muscle.

Imp protein is cytoplasmic and present in all cells of the oocyte, follicle cells, nurse cells, and the oocyte. Within the germline, the pattern changes with time. It is initially uniform in the dividing germ line cells of each cyst but becomes rapidly concentrated in the oocyte. By stage S7, the uniform levels in the oocyte are noticably reduced but by stage S8 and S9 Imp levels are elevated in a narrow zone between the nucleus and the anterior and dorsolateral margins of the oocyte (an area which coincides with the region where grk mRNA and protein accumulate). This localizaton is lost by mid-stage 9. Imp also localizes to a crescent at the posterior pole of the oocyte.

Imp protein is found in the oocyte and in nurse cells early in oogenesis but penetration of the antibody into the oocyte is blocked after stage S4.

Marker for
 
Subcellular Localization
CV Term
Evidence
References
located_in axon
inferred from direct assay
inferred from high throughput direct assay
located_in cytoplasm
inferred from high throughput direct assay
located_in cytosol
inferred from direct assay
inferred from direct assay
inferred from high throughput direct assay
Expression Deduced from Reporters
Reporter: P{lacW}130
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{PTT-un}CB02137
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{PTT-un}G00080
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{PTT-un}ImpG0171X
Stage
Tissue/Position (including subcellular localization)
Reference
Reporter: P{PTT-un}ImpG0293X
Stage
Tissue/Position (including subcellular localization)
Reference
Stage
Tissue/Position (including subcellular localization)
Reference
Stage
Tissue/Position (including subcellular localization)
Reference
Stage
Tissue/Position (including subcellular localization)
Reference
adult brain cell body rind

Comment: adult brain cortex, only around central brain

Stage
Tissue/Position (including subcellular localization)
Reference
adult brain cell body rind | restricted

Comment: expression in part of the adult brain cortex surrounding the central brain

High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\Imp 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
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
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 78 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 25 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of Imp
Transgenic constructs containing regulatory region of Imp
Aberrations (Deficiencies and Duplications) ( 4 )
Inferred from experimentation ( 4 )
Gene not disrupted in
Gene duplicated in
Inferred from location ( 8 )
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
anterior fascicle & synapse, with Scer\GAL4elav-C155
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (29)
14 of 14
Yes
Yes
3  
13 of 14
No
Yes
1  
13 of 14
No
Yes
2 of 14
No
No
1  
2 of 14
No
No
2 of 14
No
No
3  
2 of 14
No
No
2 of 14
No
No
1  
2 of 14
No
No
1  
2 of 14
No
No
2 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
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  
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
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (26)
14 of 14
Yes
Yes
13 of 14
No
Yes
12 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
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
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (25)
14 of 14
Yes
Yes
13 of 14
No
Yes
12 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
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
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (24)
7 of 13
Yes
Yes
1 of 13
No
Yes
1 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
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
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
Danio rerio (Zebrafish) (29)
14 of 14
Yes
Yes
13 of 14
No
Yes
13 of 14
No
Yes
12 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
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
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
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
Caenorhabditis elegans (Nematode, roundworm) (12)
11 of 14
Yes
Yes
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
Yes
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) (9)
12 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (16)
4 of 13
Yes
No
4 of 13
Yes
No
4 of 13
Yes
No
4 of 13
Yes
No
4 of 13
Yes
No
3 of 13
No
Yes
3 of 13
No
No
3 of 13
No
No
3 of 13
No
No
2 of 13
No
No
2 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) (3)
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
Schizosaccharomyces pombe (Fission yeast) (2)
1 of 12
Yes
No
1 of 12
Yes
No
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:Imp. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (10)
5 of 13
4 of 13
3 of 13
3 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 ( 1 )
Allele
Disease
Evidence
References
Potential Models Based on Orthology ( 1 )
Modifiers Based on Experimental Evidence ( 3 )
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.
Interactions
Summary of Physical Interactions
Interaction Browsers

Please see the Physical Interaction reports below for full details
RNA-RNA
Physical Interaction
Assay
References
RNA-protein
Physical Interaction
Assay
References
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
Pathways
Signaling Pathways (FlyBase)
Metabolic Pathways
FlyBase
External Links
External Data
Linkouts
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
X
Recombination map
1-33
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
9F1-9F4
; Limits computationally determined from genome sequence between P{EP}sesBEP319&P{EP}ImpEP760 and P{EP}EP1321EP1321&P{EP}CG2061EP1537
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
9F1-9F4
(determined by in situ hybridisation)
9C3-9C4
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location
Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (43)
Genomic Clones (13)
 

Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete

cDNA Clones (125)
 

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
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)
    RNAi and Array Information
    Linkouts
    Antibody Information
    Laboratory Generated Antibodies
    Commercially Available Antibodies
     
    Cell Line Information
    Publicly Available Cell Lines
     
      Other Stable Cell Lines
       
      • New stable cell line derived from S2R+ : A stable S2R+ cell population expressing copper-inducible GFP-Imp was created.

      Other Comments

      Imp plays no essential role in the assembly or function of the pole plasm.

      Expression is enriched in embryonic gonads.

      Relationship to Other Genes
      Source for database merge of

      Source for merge of: Imp l(1)G0072

      Source for merge of: Imp anon- EST:fe2B3

      Source for merge of: Imp MRE11

      Source for merge of: Imp FGC026A04

      Additional comments

      MRE11 is part of the 3' UTR of Imp.

      MRE11 corresponds to a portion of the 3' UTR of Imp.

      Source for merge of: Imp anon-WO0140519.39 Source for merge of Imp anon-WO0140519.39 was sequence comparison ( date:051113 ).

      Source for identity of IGF-II CG1691 was sequence comparison ( date:000414 ).

      FGC026A04 corresponds to the 3' UTR of Imp; merged in FB2017_02.

      Nomenclature History
      Source for database identify of

      Source for identity of: IGF-II CG1691

      Nomenclature comments
      Etymology
      Synonyms and Secondary IDs (24)
      Reported As
      Symbol Synonym
      IGF-II
      Imp
      (Lee et al., 2025, Meyer et al., 2024, Sood et al., 2024, Hamid et al., 2023, Nieken et al., 2023, Titlow et al., 2023, Titus et al., 2023, Voutyraki et al., 2023, Beaver et al., 2022, Cassella and Ephrussi, 2022, Guan et al., 2022, Islam and Erclik, 2022, Pushpalatha et al., 2022, Ray et al., 2022, Sreejith et al., 2022, Formicola et al., 2021, Michki et al., 2021, Rossi et al., 2021, Sood et al., 2021, To et al., 2021, Xie et al., 2021, Carrasco et al., 2020, Dold et al., 2020, Earl et al., 2020, Lepesant et al., 2020, Lopes et al., 2020, Maurange, 2020, Mira and Morante, 2020, Samuels et al., 2020, Samuels et al., 2020, Fingerhut et al., 2019, Genovese et al., 2019, Herrera and Bach, 2019, Pahl et al., 2019, Sreejith et al., 2019, van den Ameele and Brand, 2019, Vijayakumar et al., 2019, Croset et al., 2018, Davie et al., 2018, Landskron et al., 2018, Li et al., 2018, Peiris et al., 2018, Wang et al., 2018, Bonneaud et al., 2017, Doe, 2017, Hsu and Drummond-Barbosa, 2017, Sharma et al., 2017, Vallejos Baier et al., 2017, Yang et al., 2017, Clandinin and Owens, 2016-, Lee et al., 2016, Lu et al., 2016, Na et al., 2016, Narbonne-Reveau et al., 2016, Nielsen et al., 2016, Dorn and Dorn, 2015, Gene Disruption Project members, 2015-, Horan et al., 2015, Jambor et al., 2015, Khan et al., 2015, Kwong et al., 2015, Lin et al., 2015, Liu et al., 2015, Ashwal-Fluss et al., 2014, Lye et al., 2014, White-Grindley et al., 2014, de Celis et al., 2013.9.11, Hattori et al., 2013, Kwon et al., 2013, Laver et al., 2013, Lim et al., 2012, Matunis et al., 2012, McDermott et al., 2012, Toledano et al., 2012, FlyBase Genome Annotators, 2011, Friedman et al., 2011, Shimada et al., 2011, Gan et al., 2010, Müller et al., 2010, Saja et al., 2010, Wasbrough et al., 2010, Wasbrough et al., 2010, Snee and Macdonald, 2009, Boylan et al., 2008, Clouse et al., 2008, Fabrizio et al., 2008, Mensch et al., 2008, Bilen and Bonini, 2007, Buszczak et al., 2007, Geng and MacDonald, 2007, Grieder et al., 2007, Koizumi et al., 2007, Lecuyer et al., 2007, Maia et al., 2007, Quinones-Coello, 2007, Quinones-Coello et al., 2007, Geng and Macdonald, 2006, Manak et al., 2006, Terry et al., 2006)
      anon-EST:fe2B3
      anon-WO0140519.39
      cg1691
      Name Synonyms
      IGF-II messenger RNA binding protein
      Insulin-like Growth Factor 2 mRNA Binding Protein 1
      anon-fast-evolving-2B3
      insulin-like growth factor II
      mRNA-like ncRNA in embryogenesis 11
      Secondary FlyBase IDs
      • FBgn0262735
      • FBgn0030235
      • FBgn0025229
      • FBgn0026687
      • FBgn0044592
      • FBgn0086543
      • FBgn0086345
      Datasets (0)
      Study focus (0)
      Experimental Role
      Project
      Project Type
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      Study result (0)
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      External Crossreferences and Linkouts ( 123 )
      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 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.
      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.
      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
      KEGG Genes - Molecular building blocks of life in the genomic space.
      MARRVEL_MODEL - MARRVEL (model organism gene)
      Linkouts
      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
      iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
      Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
      References (234)