Gene

F18A11.3

Species
Caenorhabditis elegans
Symbol
F18A11.3
Name
UPF0729 protein F18A11.3
Synonyms
  • CELE_F18A11.3
Biotype
protein coding gene
Automated Description
Predicted to be located in plasma membrane. Orthologous to human C18orf32 (chromosome 18 open reading frame 32).
WB Description
Predicted to be located in plasma membrane. Is an ortholog of human C18orf32 (chromosome 18 open reading frame 32).
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR13456
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensC18orf322 of 9YesYes   
Mus musculusBC0311813 of 9YesYes   
Rattus norvegicusC18h18orf323 of 9YesYes   
Xenopus tropicalisc1h18orf322 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

No paralogs for the gene.

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
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
WBcel235
Viewer Help
13.03635M13.03640M13.03645M13.03650M13.03655M13.03660M13.03665M13.03670M13.03675M13.03680M
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_003280.10:g.13036470A>Tvariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036459T>Avariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036424G>Avariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036564A>Gvariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036568T>Cvariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036778T>Avariant
SNP
  • missense variant
NC_003280.10:g.13036469G>Tvariant
SNP
  • 3 prime UTR variant
NC_003280.10:g.13036368C>Avariant
SNP
  • missense variant
NC_003280.10:g.13036653G>Avariant
SNP
  • missense variant
NC_003280.10:g.13036562T>Avariant
SNP
  • 3 prime UTR variant
Showing 1 - 10 of 11 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
13.03635M13.03640M13.03645M13.03650M13.03655M13.03660M13.03665M13.03670M13.03675M13.03680MF18A11.3.1 (F18A11.3)F18A11.2.1 (F18A11.2)F18A11.2.2 (F18A11.2)F18A11.2.3 (F18A11.2)F18A11.2.4 (F18A11.2)

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