Gene

NUP210L

Species
Homo sapiens
Symbol
NUP210L
Name
nucleoporin 210 like
Synonyms
  • nuclear pore membrane glycoprotein 210-like
  • nuclear pore membrane glycoprotein 210-like (LOC91181)
Biotype
protein coding gene
Automated Description
Predicted to act upstream of or within Sertoli cell development and spermatid development. Predicted to be located in membrane. Predicted to be part of nuclear pore.
RGD Description
Predicted to act upstream of or within Sertoli cell development and spermatid development. Predicted to be located in membrane. Predicted to be part of nuclear pore. [provided by Alliance of Genome Resources, Nov 2024]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR23019
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusNup210l10 of 10YesYes  
Rattus norvegicusNup210l10 of 10YesYes  
Drosophila melanogasterGp2108 of 9YesYes   
Caenorhabditis elegansnpp-129 of 9YesYes   
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
NUP2101189562457 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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
GRCh38
Viewer Help
154.00M154.02M154.04M154.06M154.08M154.10M154.12M154.14M
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_000001.11:g.154000946C>Avariant
SNP
  • intron variant
NC_000001.11:g.154001018G>Tvariant
SNP
  • intron variant
NC_000001.11:g.154060953G>Avariant
SNP
  • missense variant
NC_000001.11:g.154000927T>Cvariant
SNP
  • intron variant
NC_000001.11:g.154060995C>Tvariant
SNP
  • missense variant
NC_000001.11:g.154089435G>Avariant
SNP
  • missense variant
NC_000001.11:g.154094963C>Tvariant
SNP
  • missense variant
NC_000001.11:g.154139824C>Tvariant
SNP
  • missense variant
NC_000001.11:g.154152755A>Cvariant
SNP
  • missense variant
NC_000001.11:g.154154957C>Tvariant
SNP
  • missense variant
Showing 1 - 10 of 79 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCh38
Viewer Help
154.00M154.02M154.04M154.06M154.08M154.10M154.12M154.14M

Sequence Details

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Expression

Primary Sources
None
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

4 interactor genes based on 4 annotations
NUP210L molecule type
Interactor gene
Interactor species
Interactor molecule type
Detection methods
Source
Reference
protein
ACLYHomo sapiens
protein
  • biochemical
PMID:26344197
protein
KIF20AHomo sapiens
protein
  • affinity chromatography technology
PMID:31586073
protein
PTPROHomo sapiens
protein
  • affinity chromatography technology
PMID:27432908
protein
TRRAPHomo sapiens
protein
  • affinity chromatography technology
PMID:35906200
Showing 1 - 4 of 4 rows
per page

Genetic Interactions

No data available