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Gene : ATXN2L Homo sapiens

Name  ? ataxin 2 like Cytological Location  16p11.2
Brief Description  ataxin 2 like
Description  This gene encodes an ataxin type 2 related protein of unknown function. This protein is a member of the spinocerebellar ataxia (SCAs) family, which is associated with a complex group of neurodegenerative disorders. Several alternatively spliced transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • A2lp,
  • HGNC:31326,
  • OTTHUMG00000097038,
  • ATXN2L,
  • A2RP,
  • A2D,
  • A2LG,
  • A2LP,
  • uc002dqy.5,
  • A2D,
  • ataxin 2-like,
  • NM_007245
  • identifiers:
  • 11273,
  • ENSG00000168488,
  • ATXN2L

Genome feature

Region: gene ? Length: 14239  
Location: 16:28822999-28837237 Cyto location: 16p11.2

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

566 SN Ps

5 Cross References

17 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results