Gene

CG32263

Species
Drosophila melanogaster
Symbol
CG32263
Name
Not Available
Synonyms
  • CG10854
Biotype
protein coding gene
Automated Description
Predicted to enable monoatomic ion channel activity. Predicted to be involved in mitochondrial ribosome assembly and monoatomic ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in mitochondrion. Orthologous to human MPV17L2 (MPV17 mitochondrial inner membrane protein like 2).
FB Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11266
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensMPV17L25 of 9YesNo   
Mus musculusMpv17l25 of 9YesNo   
Rattus norvegicusMpv17l26 of 9YesYes   
Danio reriompv17l23 of 10YesNo  
Caenorhabditis elegansZK470.14 of 9YesNo   
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
CG32262120956415 of 8  
CG5906219750335 of 8  
CG1662316756375 of 8  
plh417247282 of 8  
CG14778517149252 of 8  
CG14777615251282 of 8  
Mpv17716446272 of 8  
CG7970817345242 of 8  

Function - GO Annotations

No function available for that gene

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
3.8104M3.8105M3.8106M3.8107M3.8108M3.8109M3.8110M3.8111M
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
CG32263c02814
  • CG32263[c02814]
allele with one associated variant
insertion
  • 3 prime UTR variant
NT_037436.4:g.3810686A>Gvariant
SNP
  • synonymous variant
NT_037436.4:g.3810776C>Tvariant
SNP
  • synonymous variant
NT_037436.4:g.3810319G>Cvariant
SNP
  • 3 prime UTR variant
NT_037436.4:g.3810434G>Avariant
SNP
  • synonymous variant
NT_037436.4:g.3811034T>Cvariant
SNP
  • 5 prime UTR variant
NT_037436.4:g.3811102G>Avariant
SNP
  • 5 prime UTR variant
NT_037436.4:g.3810974T>Cvariant
SNP
  • 5 prime UTR variant
NT_037436.4:g.3810992G>Cvariant
SNP
  • 5 prime UTR variant
NT_037436.4:g.3810554C>Tvariant
SNP
  • synonymous variant
Showing 1 - 10 of 57 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 melanogasterCG32263GD2283
  • UASt
Drosophila melanogasterCG32263KK106642
  • UASt
Drosophila melanogasterCG32263NIG.10854R
  • UASt
Showing 1 - 3 of 3 rows
per page

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
R6
Viewer Help
3.8104M3.8105M3.8106M3.8107M3.8108M3.8109M3.8110M3.8111MCG32263-RA (CG32263)

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