FlyAtlas 2 – Gene
For a particular Drosophila gene, find the pattern of expression in different tissues.
 
Gene Symbol (e.g. vkg) — start typing, then select from the autosuggest menu
Gene Name (e.g. viking)
Annotation Symbol (e.g. CG16858)
Gene ID (e.g. FBgn0016075)
Transcript ID (e.g. FBtr0079036)

Gene:

Symbol
chp
Name
chaoptin
Annotation Symbol
CG1744
FlyBase ID
FBgn0267435
Paralogues
Paralogues(s)
link out
SDs   Whole Body   Male v. Female
Gene FPKMs and Enrichments 
Adult MaleAdult FemaleMale v. FemaleLarval
TissueFPKMEnrichmentFPKMEnrichmentM/Fp valueFPKMEnrichment
Head122 ± 9.15.1116 ± 25191.05n.s.  
Eye739 ± 16531455 ± 75731.63n.s.  
Brain / CNS0.5 ± 0.30.00.8 ± 0.00.11.00n.s.0.7 ± 0.2N.A.
Thoracicoabdominal ganglion0.1 ± 0.00.00.2 ± 0.00.01.00n.s.  
Crop0.9 ± 0.70.01.4 ± 0.70.21.00n.s.  
Midgut0.1 ± 0.10.00.0 ± 0.00.01.00n.s.0.1 ± 0.0N.A.
Hindgut0.0 ± 0.10.00.0 ± 0.00.01.00n.s.0.1 ± 0.1N.A.
Malpighian Tubules0.2 ± 0.10.00.1 ± 0.10.01.00n.s.0.0 ± 0.0N.A.
Rectal pad0.0 ± 0.00.00.2 ± 0.20.01.00n.s.  
Salivary gland2.4 ± 0.70.11.5 ± 0.20.21.22n.s.0.0 ± 0.0N.A.
Fat body0.1 ± 0.10.00.2 ± 0.20.01.00n.s.0.0 ± 0.0N.A.
Heart0.0 ± 0.00.00.1 ± 0.10.01.00n.s.  
Trachea      0.1 ± 0.1N.A.
Ovary  0.1 ± 0.00.0    
Virgin Spermatheca  0.4 ± 0.30.1    
Mated Spermatheca  0.1 ± 0.10.0    
Testis0.3 ± 0.10.0      
Accessory glands8.5 ± 0.90.4      
Carcass0.4 ± 0.50.00.2 ± 0.20.01.00n.s.0.2 ± 0.0N.A.
Garland cells      0.1 ± 0.1N.A.
Whole body24 ± 2.06.2 ± 0.73.9p < 0.010.2 ± 0.1
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Rotate to see Transcript Table
TranscriptMaleFemaleLarval
NameIDHdEyBrTgCrMgHgTuRpSgFbHtTsAgCsHdEyBrTgCrMgHgTuRpSgFbHtOvVsMsCsNsMgHgTuSgFbTrCsGa
RAFBtr0085778
RCFBtr0330100
REFBtr0335410
RFFBtr0335411
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*Tissue Comparability: See Docs for info on the chemistry used to sequence different tissues.
WARNING: Transcript Ambiguity for this Gene!
Because FlyBase assigns a unique transcript name and identifier for each unique protein, the rare cases in which such proteins result from alternative translation of the same mRNA give rise to situations in which there are two or more different identifiers for the same physical transcript. RNAseq analysis can only deal with unique sequences, and in such cases arbitrarily assigns the data from a sequence to one of the different transcript identifiers. The result is that some named transcripts will be missing, or data for some transcripts will actually include that for others. In the case of gene FBgn0267435 the situation is:

No data for FBtr0330101 — included in FBtr0335411: Alternative Stop codons (readthrough)

*** More extensive information about transcript ambiguity and its implications can be found in the Docs ***