Gene

oac-55

Species
Caenorhabditis elegans
Symbol
oac-55
Name
O-ACyltransferase homolog 55
Synonyms
  • CELE_Y39H10A.2
  • Y39H10A.2
Biotype
protein coding gene
Automated Description
Predicted to enable acyltransferase activity, transferring groups other than amino-acyl groups. Predicted to be located in membrane.
WB Description
Predicted to enable acyltransferase activity, transferring groups other than amino-acyl groups. Predicted to be located in membrane.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11161
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusOacyl3 of 9YesNo   
Rattus norvegicusOacyl4 of 9YesNo   
Danio reriooacyl4 of 9YesNo   
Drosophila melanogasterCG304712 of 9YesYes   
Drosophila melanogasterCG129902 of 9YesYes   
Drosophila melanogasterCG113532 of 9YesYes   
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
oac-39174681676 of 8  
oac-6279146285 of 8  
oac-31376945285 of 8  
oac-32468748305 of 8  
oac-14569247285 of 8  
oac-20667848285 of 8  
nrf-6782443234 of 8  
oac-7866548315 of 8  
oac-5969846275 of 8  
oac-31071945284 of 8  
oac-531169845284 of 8  
oac-501262743253 of 8  
oac-91375037212 of 8  
oac-461457244253 of 8  
ndg-41567938202 of 8  
oac-541650142233 of 8  
rhy-11753839213 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None
No data available

Disease Associations

Cases where the expected disease association was NOT found
all annotationsall disease by infectious agentbacterial infectious diseasefungal infectious diseaseparasitic infectious diseaseviral infectious diseaseall disease of anatomical entitycardiovascular system diseasecentral nervous system diseaseendocrine system diseasegastrointestinal system diseasehematopoietic system diseaseimmune system diseaseintegumentary system diseasemusculoskeletal system diseaseperipheral nervous system diseasereproductive system diseaserespiratory system diseasesensory system diseasethoracic diseaseurinary system diseaseall disease of cellular proliferationbenign neoplasmcancerpre-malignant neoplasmall genetic diseasechromosomal diseasemonogenic diseasepolygenic diseaseall other diseasedisease of mental healthdisease of metabolismphysical disordersyndrome
oac-55 (Cel)
Oacyl (Mmu)
Oacyl (Rno)
oacyl (Dre)
CG11353 (Dme)
CG12990 (Dme)
CG30471 (Dme)
Cell color indicative of annotation volume
No data available

Alleles and Variants

Genome location
Assembly version
WBcel235
Viewer Help
3.7615M3.7620M3.7625M3.7630M3.7635M3.7640M3.7645M3.7650M3.7655M3.7660Moac-55Y39H10A.2a.1Y39H10A.2b.1Y39H10A.2c.1Y39H10A.8Y39H10A.8
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
NC_003283.11:g.3764866G>Avariant
SNP
  • synonymous variant
NC_003283.11:g.3761747T>Avariant
SNP
  • splice region variant
NC_003283.11:g.3763426T>Gvariant
SNP
  • intron variant
NC_003283.11:g.3763460C>Tvariant
SNP
  • intron variant
NC_003283.11:g.3764015C>Avariant
SNP
  • intron variant
NC_003283.11:g.3764700T>Cvariant
SNP
  • synonymous variant
NC_003283.11:g.3765588C>Tvariant
SNP
  • synonymous variant
NC_003283.11:g.3761657C>Tvariant
SNP
  • missense variant
NC_003283.11:g.3765759C>Tvariant
SNP
  • intron variant
NC_003283.11:g.3761374A>Tvariant
SNP
  • intron variant
Showing 1 - 10 of 108 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
3.7615M3.7620M3.7625M3.7630M3.7635M3.7640M3.7645M3.7650M3.7655M3.7660MY39H10A.2a.1 (oac-55)Y39H10A.2b.1 (oac-55)Y39H10A.2c.1 (oac-55)Y39H10A.8

Sequence Details

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Expression

Primary Sources
Other Sources
all annotationsall anatomical structuresalimentary part of gastrointestinal systemchemosensory systemcirculatory systemendocrine systemexocrine systemhemolymphoid systemhepatobiliary systemintegumental systemmechanosensory systemmusculoskeletal systemnervous systemrenal systemreproductive systemrespiratory systemsensory systemvestibulo-auditory systemvisual systemendodermectodermmesodermmesenchymeadipose tissueappendageentire extraembryonic componentimaginal precursorpharyngeal archotherall stagesembryo stagepost embryonic, pre-adultpost-juvenile adult stageall cellular componentsextracellular regionplasma membranesynapsecell junctioncell projectioncytoplasmic vesicleendosomevacuolegolgi apparatusendoplasmic reticulumcytosolmitochondrionnucleuschromosomecytoskeletonprotein-containing complexother locations
oac-55 (Cel)
oacyl (Dre)
CG11353 (Dme)
CG12990 (Dme)
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