Gene

nup35

Species
Danio rerio
Symbol
nup35
Name
nucleoporin 35
Synonyms
  • fj68d11
  • wu:fj68d11
Biotype
protein coding gene
Automated Description
Predicted to enable phospholipid binding activity. Predicted to be a structural constituent of nuclear pore. Predicted to be involved in NLS-bearing protein import into nucleus and nuclear pore organization. Predicted to act upstream of or within nucleocytoplasmic transport and protein transport. Predicted to be located in nuclear membrane. Predicted to be part of nuclear pore central transport channel and nuclear pore nuclear basket. Orthologous to human NUP35 (nucleoporin 35).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR21527
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensNUP3510 of 10YesYes  
Mus musculusNup3510 of 10YesYes  
Rattus norvegicusNup359 of 9YesYes   
Xenopus tropicalisnup359 of 9YesYes   
Drosophila melanogasterNup359 of 10YesYes  
Caenorhabditis elegansnpp-196 of 9YesYes   
Saccharomyces cerevisiaeNUP534 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
GRCz11
Viewer Help
12.260M12.261M12.262M12.263M12.264M12.265M12.266M12.267M12.268M12.269M
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
sa21442allele with one associated variant
point mutation
  • stop gained
Showing 1 - 1 of 1 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCz11
Viewer Help
12.260M12.261M12.262M12.263M12.264M12.265M12.266M12.267M12.268M12.269Mnup35-201 (nup35)nup35-202 (nup35)nup35-203 (nup35)nup35-204 (nup35)nup35-205 (nup35)

Sequence Details

Loading...

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