Gene

ZK858.5

Species
Caenorhabditis elegans
Symbol
ZK858.5
Name
TM2 domain-containing protein ZK858.5
Synonyms
  • CELE_ZK858.5
Biotype
protein coding gene
Automated Description
Predicted to be active in membrane. Orthologous to human DNAJC22 (DnaJ heat shock protein family (Hsp40) member C22).
WB Description
Predicted to be located in membrane. Is an ortholog of human DNAJC22 (DnaJ heat shock protein family (Hsp40) member C22).
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR21016
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensDNAJC222 of 9YesYes   
Rattus norvegicusDnajc222 of 9YesYes   
Xenopus tropicalisdnajc222 of 9YesYes   
Drosophila melanogasterwus2 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

No function available for that gene

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
9.1360M9.1365M9.1370M9.1375M9.1380M
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_003279.8:g.9136096G>Avariant
SNP
  • missense variant
NC_003279.8:g.9136869C>Tvariant
SNP
  • intron variant
NC_003279.8:g.9136125C>Tvariant
SNP
  • missense variant
NC_003279.8:g.9136569G>Avariant
SNP
  • intron variant
NC_003279.8:g.9136756T>Avariant
SNP
  • splice region variant
NC_003279.8:g.9136879G>Avariant
SNP
  • intron variant
NC_003279.8:g.9137638G>Avariant
SNP
  • splice region variant
NC_003279.8:g.9137540A>Gvariant
SNP
  • missense variant
NC_003279.8:g.9138028A>Gvariant
SNP
  • intron variant
NC_003279.8:g.9136948T>Avariant
SNP
  • missense variant
Showing 1 - 10 of 20 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
9.1360M9.1365M9.1370M9.1375M9.1380M

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