Gene

H24K24.2

Species
Caenorhabditis elegans
Symbol
H24K24.2
Name
Protein NLRC3
Synonyms
  • CELE_H24K24.2
Biotype
protein coding gene
Automated Description
Predicted to be part of Cul2-RING ubiquitin ligase complex.
WB Description
Predicted to be part of Cul2-RING ubiquitin ligase complex.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR12904
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
gadr-2149550324 of 8  
H04D03.4252946284 of 8  
Y55F3C.9349848304 of 8  
C48D1.1447052304 of 8  
F53G2.1548651284 of 8  
K05C4.9647751284 of 8  
gadr-4745652314 of 8  
gadr-3846551304 of 8  
gadr-5947547284 of 8  
Y9C9A.131047847274 of 8  
F44E5.21143352304 of 8  
zeel-11246846284 of 8  
gadr-61345047274 of 8  
Y71A12B.121449243253 of 8  
K05C4.31543746273 of 8  
zyg-111649742262 of 8  
zer-11747937212 of 8  
Y39A1A.171819656372 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
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
WBcel235
Viewer Help
918k919k920k921k922k923k924k925k926k
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.920320C>Tvariant
SNP
  • intron variant
NC_003283.11:g.923324G>Avariant
SNP
  • intron variant
NC_003283.11:g.920970T>Cvariant
SNP
  • intron variant
NC_003283.11:g.918049A>Tvariant
SNP
  • intron variant
NC_003283.11:g.925220T>Avariant
SNP
  • intron variant
NC_003283.11:g.918149C>Tvariant
SNP
  • intron variant
NC_003283.11:g.923874A>Gvariant
SNP
  • intron variant
NC_003283.11:g.924021G>Avariant
SNP
  • intron variant
NC_003283.11:g.924471T>Avariant
SNP
  • splice region variant
NC_003283.11:g.918129C>Avariant
SNP
  • intron variant
Showing 1 - 10 of 137 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
918k919k920k921k922k923k924k925k926kH24K24.2a.1 (H24K24.2)H24K24.2b.1 (H24K24.2)H24K24.2c.1 (H24K24.2)H24K24.2d.1 (H24K24.2)H24K24.6 (21ur-11651)

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