FB2026_02 , released June 18, 2026
Gene: Dmel\RanGAP
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General Information
Symbol
Dmel\RanGAP
Species
D. melanogaster
Name
Ran GTPase activating protein
Annotation Symbol
CG9999
Feature Type
FlyBase ID
FBgn0003346
Gene Model Status
Stock Availability
Gene Summary
GTPase activator for the nuclear Ras-related regulatory protein Ran, converting it to the putatively inactive GDP-bound state (By similarity). Trans-acting factor necessary for meiotic distortion (PubMed:10073941). Distortion is only seen in individuals that carry the RanGAP tandem duplication and express a RanGAP truncated protein. Binding of truncated RanGAP product to the Responder(RSP) locus initiates events that lead to sperm dysfunction (PubMed:10073941). During oogenesis, plays a role in the biogenesis of annulate lamellae containing nuclear pore complex components (PubMed:31626769). (UniProt, Q9VIW3)
Contribute a Gene Snapshot for this gene.
Also Known As

Sd, Segregation distorter, Sd-RanGAP

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
2-54
RefSeq locus
NT_033779 REGION:19441959..19447317
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (14 terms)
Molecular Function (3 terms)
Terms Based on Experimental Evidence (2 terms)
CV Term
Evidence
References
inferred from direct assay
enables RNA binding
inferred from direct assay
Terms Based on Predictions or Assertions (2 terms)
CV Term
Evidence
References
inferred from electronic annotation with InterPro:IPR027038, InterPro:IPR036720
inferred from biological aspect of ancestor with PANTHER:PTN001536945
inferred from biological aspect of ancestor with PANTHER:PTN001536945
Biological Process (6 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
traceable author statement
involved_in nuclear export
inferred from biological aspect of ancestor with PANTHER:PTN001536945
non-traceable author statement
inferred from electronic annotation with InterPro:IPR036720
Cellular Component (5 terms)
Terms Based on Experimental Evidence (2 terms)
CV Term
Evidence
References
located_in cytoplasm
inferred from direct assay
inferred from direct assay
Terms Based on Predictions or Assertions (4 terms)
CV Term
Evidence
References
is_active_in cytosol
inferred from biological aspect of ancestor with PANTHER:PTN001536945
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN001536945
inferred from biological aspect of ancestor with PANTHER:PTN001536945
Gene Group (FlyBase)
Protein Family (UniProt)
Belongs to the RNA1 family. (Q9VIW3)
Summaries
Gene Group (FlyBase)
RAN GTPASE ACTIVATING PROTEINS -
RanGAP promotes conversion of Ran-GTP to Ran-GDP on cytosolic side of the nuclear pore as part of the nucleocytoplasmic transport shuttling cycle of Ran. (Adapted from PMID:15731001).
Protein Function (UniProtKB)
GTPase activator for the nuclear Ras-related regulatory protein Ran, converting it to the putatively inactive GDP-bound state (By similarity). Trans-acting factor necessary for meiotic distortion (PubMed:10073941). Distortion is only seen in individuals that carry the RanGAP tandem duplication and express a RanGAP truncated protein. Binding of truncated RanGAP product to the Responder(RSP) locus initiates events that lead to sperm dysfunction (PubMed:10073941). During oogenesis, plays a role in the biogenesis of annulate lamellae containing nuclear pore complex components (PubMed:31626769).
(UniProt, Q9VIW3)
Phenotypic Description (Red Book; Lindsley and Zimm 1992)
Sd: Segregation distorter
Sd-bearing second chromosomes are referred to as SD; they carry, in addition to Sd, other components of the segregation distortion system; they may carry inversions and recessive lethal alleles as well. The constitutions of various SD chromosomes are tabulated below. Other components of the segregation distortion system are E(SD) (Enhancer of SD) at the base of 2L; and Rsp (Responder) at the base of 2R; St(SD) (Stabilizer of SD) located more distally in 2R appears to comprise several weak enhancers of distortion (Miklos, 1972, Genetics 70: 405-18). All naturally occurring SD chromosomes carry Sd and E(SD) but lack Rsp [sometimes said to carry Rspi (Responder insensitive)]; most normal chromosomes carry a Rsp element. SD/+ males transmit SD-bearing, to the virtual exclusion of +-bearing, homologues; as many as 99% of the functional sperm may carry SD (defined as k = .99). The sex ratio of the minority class of offspring, in diverse crosses, is skewed in proportion to k in such a way as to indicate that within this class the probability of recovery of XY- < X - < Y -bearing <nullo-X, nullo-Y sperm (Denell, Judd, and Richardson, 1969, Genetics 61: 129-39; Denell and Miklos, 1971, Mol. Gen. Genet. 110: 167-77). Distortion by Sd requires heterozygosity at the Rsp locus; when Rsp is on the homologue, the Sd-bearing chromosome is preferentially recovered. and when Rsp and Sd are in coupling, the homologue is recovered preferentially. Extensive electron microscopic studies of spermatogenesis (Tokuyasu, Peacock, and Hardy, 1972, Z. Zellforsch. 124: 479-506; 127: 492-525; 1977, J. Ultrastruct. Res. 48: 284-303) demonstrate that spermiogenesis of SD/+ males is defective; chromatin in half of the spermatid nuclei fails to condense properly, leading in some cases to a failure of the spermatids to become individually invested in membrane, remaining syncytial instead, and in all cases to incomplete maturation of half the sperm. In addition, the transition from lysine-rich to sperm-specific arginine-rich histone, which normally occurs in late spermiogenesis, does not appear to take place in half the spermatids of SD/+ males (Hauschteck-Jungen and Hartl, 1978, Genetics 101: 57-69). Temperature-sensitive period of distortion said to be in the primary spermatocyte (Mange, 1968, Genetics 58: 399-413); however, see Matthews and Mortin (1983, Canad. J. Genet. Cytol. 25: 662-67). k values also reported to increase with time of storage of sperm by females (Hartl, 1973, Genetics 74: 619-31), to decrease with the age of SD/+ males (Hiraizumi and Watanabe, 1969, Genetics 63: 212-31), and to be influenced by the genotype of the female to which such males are crossed (Denell and Judd, 1969, Mol. Gen. Genet. 105: 262-74). Segregation distortion is subject to modification by numerous genetic factors throughout the genome; in addition various abnormal chromosome constitutions have been reported to reduce k values (Novitski and Erlich, 1970, DIS 45: 102; Enns, 1970, DIS 45: 136; Fowler, 1971, DIS 46: 74). Homozygous (when viable) and heteroallelic constitutions exhibit variably reduced male fertility, but the contribution of Sd vis a vis other components of the SD chromosomes involved not easily ascertainable. SD chromosomes without effect in females.
Gene Model and Products
Number of Transcripts
3
Number of Unique Polypeptides
2

Please see the JBrowse view of Dmel\RanGAP 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 Q9VIW3)

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 5.47

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0081234
2401
596
FBtr0334174
2008
596
FBtr0334175
2144
588
Additional Transcript Data and Comments
Reported size (kB)

2.0 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0080775
66.1
596
4.29
Polypeptides with Identical Sequences

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

596 aa isoforms: RanGAP-PA, RanGAP-PB
Additional Polypeptide Data and Comments
Reported size (kDa)

596 (aa); 66 (kD observed)

Comments
External Data
Subunit Structure (UniProtKB)

Forms a complex with Nup358/RanBP2, sbr/Nxf1 and Nxt1 (PubMed:14729961). Associates with the nuclear pore complex via its interaction with Nup358/RanBP2 (PubMed:14729961, PubMed:17032737).

(UniProt, Q9VIW3)
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\RanGAP 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).

0.66

Transcript Expression
No Assay Recorded
Stage
Tissue/Position (including subcellular localization)
Reference
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
organism

Comment: maternally deposited

northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
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
western blot
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

RanGAP is widely detected in neuroblasts and other cells in the central brain and optic lobes in third istar larvae. It is found in both type I and type II neuroblasts. Expression becomes more restricted in the pupal brain. It is found in the cytoplasm and or in a nuclear-membrane-bound SUMOylated form.

Rcc1 protein localizes around the outside of the karyosome in the oocyte.

The protein is localized to the cytoplamic side of the nuclear membrane in both adult testis cells and larval salivary gland cells.

Marker for
 
Subcellular Localization
CV Term
Evidence
References
located_in cytoplasm
inferred from direct assay
inferred from direct assay
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\RanGAP 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) 7-8
  • Stages(s) 9-10
  • Stages(s) 11-12
  • Stages(s) 13-16
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 17 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 20 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of RanGAP
Transgenic constructs containing regulatory region of RanGAP
Aberrations (Deficiencies and Duplications) ( 38 )
Inferred from experimentation ( 38 )
Gene partially duplicated in
Inferred from location ( 15 )
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
Other Phenotypes
Allele
Phenotype manifest in
Allele
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (19)
13 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
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
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (9)
13 of 14
Yes
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (9)
12 of 14
Yes
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (8)
10 of 13
Yes
Yes
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
Danio rerio (Zebrafish) (41)
13 of 14
Yes
Yes
13 of 14
Yes
Yes
2 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
Yes
Caenorhabditis elegans (Nematode, roundworm) (2)
8 of 14
Yes
Yes
1 of 14
No
No
Anopheles gambiae (African malaria mosquito) (2)
11 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (5)
8 of 13
Yes
Yes
7 of 13
No
Yes
4 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
Saccharomyces cerevisiae (Brewer's yeast) (1)
11 of 13
Yes
Yes
Schizosaccharomyces pombe (Fission yeast) (1)
10 of 12
Yes
Yes
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:RanGAP. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Human Disease Associations
FlyBase Human Disease Model Reports
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 0 )
    Allele
    Disease
    Evidence
    References
    Potential Models Based on Orthology ( 0 )
    Human Ortholog
    Disease
    Evidence
    References
    Modifiers Based on Experimental Evidence ( 5 )
    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.
    Homo sapiens (Human)
    Gene name
    Score
    OMIM
    OMIM Phenotype
    DO term
    Complementation?
    Transgene?
    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
    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
    Subunit Structure (UniProtKB)
    Forms a complex with Nup358/RanBP2, sbr/Nxf1 and Nxt1 (PubMed:14729961). Associates with the nuclear pore complex via its interaction with Nup358/RanBP2 (PubMed:14729961, PubMed:17032737).
    (UniProt, Q9VIW3 )
    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
    External Data
    Linkouts
    KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
    Reactome - An open-source, open access, manually curated and peer-reviewed pathway database.
    Class of Gene
    Genomic Location and Detailed Mapping Data
    Chromosome (arm)
    2L
    Recombination map
    2-54
    Cytogenetic map
    Sequence location
    FlyBase Computed Cytological Location
    Cytogenetic map
    Evidence for location
    37E1-37E1
    Limits computationally determined from genome sequence between P{EP}dntEP2158 and P{EP}EP623&P{PZ}spi01068
    Experimentally Determined Cytological Location
    Cytogenetic map
    Notes
    References
    37D3-37D5
    (determined by in situ hybridisation)
    Experimentally Determined Recombination Data
    Location
    Left of (cM)
    Right of (cM)
    Notes
    Stocks and Reagents
    Stocks (15)
    Genomic Clones (17)
     

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

    cDNA Clones (59)
     

    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)
    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

        aub mutations act as genetic enhancers of Segregation Distorter. This effect is still seen when aub mutations are targeted (by homologous recombination) to the Dp(2;2)RanGAPSD chromosome, indicating that the effect of aub mutations is not specific to the target Rsp-bearing chromosome.

        Area matching Drosophila gene RanGAP, Acc. No. AF143860.

        The truncated RanGap product encoded by SD distorting chromosomes (RanGapSD) retains normal enzyme activity, but has abnormal subcellular location, being distributed diffusely throughout the cytoplasm and also having a distinct nuclear component in primary spermatocytes and salivary gland cells. Mislocalisation of the active RanGapSD product to the nucleus is responsible for segregation distortion (distortion is abolished if enzymatic activity or nuclear localisation of the RanGapSD product is perturbed).

        SD chromosomes have a tandem duplication at the RanGap locus. Distortion is caused by a truncated RanGap product encoded by the distal half of the duplication.

        A mutation of RanGap generated by loss of a P-element in RanGap exhibits a maternal effect embryonic lethal phenotype. Homozygous females are completely normal but hemizygotes are sterile regardless of the genotype of the male. Embryos from these females die before the syncytial blastoderm stage, around the 7th or 8th nuclear division. In addition, their nuclei are no longer mitotically synchronous and many appear abnormal in size and shape.

        Encodes a Ran GTPase activator.

        Relationship to Other Genes
        Source for database merge of
        Additional comments
        Nomenclature History
        Source for database identify of

        Source for identity of: RanGAP RanGap

        Nomenclature comments

        'RanGap' changed to 'RanGAP' to capitalize the 'GAP' to be consistent with all other GAP gene symbols.

        Etymology
        Synonyms and Secondary IDs (24)
        Reported As
        Symbol Synonym
        Secondary FlyBase IDs
          Datasets (0)
          Study focus (0)
          Experimental Role
          Project
          Project Type
          Title
          Study result (0)
          Result
          Result Type
          Title
          External Crossreferences and Linkouts ( 56 )
          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/Swiss-Prot - Manually annotated and reviewed records of protein sequence and functional information
          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
          FlyMet - A comprehensive tissue-specific metabolomics resource for Drosophila.
          iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
          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 - An open-source, open access, manually curated and peer-reviewed pathway database.
          References (245)