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Standards Ontologies Notations
Guidelines
MIRAGE
ataxin 2

Summary
Gene Symbol
  • ATXN2
Organism
Homo sapiens (human)
NCBI Gene
6311
PubChem
6311
Alliance of Genome Resources
JoGo
ATXN2
TogoVar
ATXN2
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Amyotrophic lateral sclerosis
  • Cytoplasm
  • Isopeptide bond
  • Methylation
  • Parkinsonism
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Spinocerebellar ataxia
  • Triplet repeat expansion
  • Ubl conjugation
Proteins
Displaying all 5 entries
UniProt Protein Name
A0A5F9ZI57
Q99700
  • Spinocerebellar ataxia type 2 protein
  • Trinucleotide repeat-containing gene 13 protein
V9GY86
F8VQP2
Q2M2R5
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 7 in total
GO Term Evidence Code PMID
negative regulation of receptor internalization
regulation of translation
RNA metabolic process
P-body assembly
stress granule assembly
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
Ataxin-2
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
stress granule assembly
Displaying all 4 entries
InterPro
Ataxin 2, SM domain
Ataxin-2, C-terminal
Ataxin2-like
LsmAD domain
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0050955 spinocerebellar ataxia 2
DOID:0060892 late onset Parkinson's disease
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 6, 2026