Gene

Nol8

Species
Rattus norvegicus
Symbol
Nol8
Name
nucleolar protein 8
Synonyms
  • LOC361221
  • NEWGENE_1309551
Biotype
protein coding gene
Automated Description
Predicted to enable RNA binding activity. Predicted to be involved in protein localization to nucleolus and rRNA processing. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in chromosome. Predicted to be active in nucleolus. Orthologous to human NOL8 (nucleolar protein 8).
RGD Description
Predicted to enable RNA binding activity. Predicted to be involved in protein localization to nucleolus and rRNA processing. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in chromosome. Predicted to be active in nucleolus. Orthologous to human NOL8 (nucleolar protein 8); INTERACTS WITH (+)-schisandrin B; 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR48029
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensNOL810 of 10YesYes  
Mus musculusNol89 of 9YesYes   
Xenopus tropicalisnol89 of 9YesYes   
Danio rerionol89 of 9YesYes   
Drosophila melanogasterCG142305 of 9YesYes   
Caenorhabditis elegansK07F5.143 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
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
Nol8 (Rno)
Cell color indicative of annotation volume
No data available

Alleles and Variants

Genome location
Assembly version
mRatBN7.2
Viewer Help
14.992M14.994M14.996M14.998M15.000M15.002M15.004M15.006M15.008M15.010M15.012M
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_051352.1:g.15013474G>Avariant
SNP
  • 5 prime UTR variant
NC_051352.1:g.14998181C>Tvariant
SNP
  • intron variant
NC_051352.1:g.15013616C>Tvariant
SNP
  • 5 prime UTR variant
NC_051352.1:g.14998808C>Tvariant
SNP
  • intron variant
NC_051352.1:g.15001118C>Avariant
SNP
  • intron variant
NC_051352.1:g.14991616C>Tvariant
SNP
  • intron variant
NC_051352.1:g.14995866T>Cvariant
SNP
  • intron variant
NC_051352.1:g.15009407A>Gvariant
SNP
  • intron variant
NC_051352.1:g.15002312C>Tvariant
SNP
  • intron variant
NC_051352.1:g.15008847C>Tvariant
SNP
  • intron variant
Showing 1 - 10 of 77 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
14.992M14.994M14.996M14.998M15.000M15.002M15.004M15.006M15.008M15.010M15.012M

Sequence Details

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Expression

Primary Sources
None
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
Nol8 (Rno)
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