Gene

neurl4

Species
Danio rerio
Symbol
neurl4
Name
neuralized E3 ubiquitin protein ligase 4
Synonyms
  • sb:eu380
Biotype
protein coding gene
Automated Description
Predicted to enable ubiquitin protein ligase activity. Orthologous to human NEURL4 (neuralized E3 ubiquitin protein ligase 4).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR12429
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensNEURL410 of 10YesYes  
Mus musculusNeurl410 of 10YesYes  
Rattus norvegicusNeurl49 of 9YesYes   
Xenopus tropicalisneurl49 of 9YesYes   
Drosophila melanogasterNeurl49 of 10YesYes  
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
neurl1b156037223 of 8  
neurl1ab246339233 of 8  
neurl1aa348037213 of 8  
neurl2430038232 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
GRCz11
Viewer Help
22.46M22.47M22.48M22.49M22.50M
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
sa22090allele with one associated variant
point mutation
  • stop gained
sa22091allele with one associated variant
point mutation
  • splice donor variant
sa22092allele with one associated variant
point mutation
  • stop gained
sa22093allele with one associated variant
point mutation
  • intron variant
sa31873allele with one associated variant
point mutation
  • stop gained
sa6252allele with one associated variant
point mutation
  • stop gained
Showing 1 - 6 of 6 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCz11
Viewer Help
22.46M22.47M22.48M22.49M22.50M

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