Gene

CG11251

Species
Drosophila melanogaster
Symbol
CG11251
Name
Not Available
Synonyms
None
Biotype
protein coding gene
Automated Description
Predicted to enable acetylpyruvate hydrolase activity. Orthologous to human FAHD2A (fumarylacetoacetate hydrolase domain containing 2A) and FAHD2B (fumarylacetoacetate hydrolase domain containing 2B).
FB Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR42796
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensFAHD2B5 of 9YesNo   
Homo sapiensFAHD2A5 of 9YesNo   
Mus musculusFahd2a5 of 9YesNo   
Rattus norvegicusFahd2a5 of 9YesNo   
Xenopus tropicalisfahd2a5 of 9YesNo   
Danio reriofahd2a5 of 10YesNo  
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
CG6028129164455 of 8  
CG5793221852312 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
No data available

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
R6
Viewer Help
13.0886M13.0888M13.0890M13.0892M13.0894M13.0896M13.0898M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NT_037436.4:g.13089892A>Tvariant
SNP
  • 5 prime UTR variant
NT_037436.4:g.13089613G>Tvariant
SNP
  • synonymous variant
NT_037436.4:g.13089178G>Avariant
SNP
  • synonymous variant
NT_037436.4:g.13089228G>Cvariant
SNP
  • missense variant
NT_037436.4:g.13088603T>Cvariant
SNP
  • 3 prime UTR variant
NT_037436.4:g.13089175C>Tvariant
SNP
  • synonymous variant
NT_037436.4:g.13089715G>Avariant
SNP
  • synonymous variant
NT_037436.4:g.13089819A>Gvariant
SNP
  • missense variant
NT_037436.4:g.13088730T>Avariant
SNP
  • 3 prime UTR variant
NT_037436.4:g.13088881A>Gvariant
SNP
  • synonymous variant
Showing 1 - 10 of 50 rows
per page

Transgenic Alleles

Species
(carrying the transgene)
Allele symbol
Transgenic construct
Expressed components
Knock-down targets
Regulatory regions
Has Disease Annotations
Has Phenotype Annotations
Drosophila melanogasterCG11251GD7252
  • UASt
Drosophila melanogasterCG11251HMC06110
  • UAS
Drosophila melanogasterCG11251KK104730
  • UASt
Drosophila melanogasterCG11251NIG.11251R
  • UASt
Drosophila melanogasterCG11251TKO.GS05354
Drosophila melanogasterCG11251UAS.ORF.GW.Tag:HA
  • UASt
Showing 1 - 6 of 6 rows
per page

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
R6
Viewer Help
13.0886M13.0888M13.0890M13.0892M13.0894M13.0896M13.0898MCG11251-RA (CG11251)lncRNA:CR45749-RA (lncRNA:CR45749)

Sequence Details

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Expression

Primary Sources
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available