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Protein Coding Gene : Atxn1l ataxin 1-like

Primary Identifier  MGI:3694797 Organism  mouse, laboratory
Chromosome  8 NCBI Gene Number  52335
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables POZ domain binding activity. Involved in brain development; learning or memory; and social behavior. Acts upstream of or within several processes, including lung alveolus development; negative regulation of transcription by RNA polymerase II; and positive regulation of hematopoietic stem cell proliferation. Predicted to be located in nucleolus and nucleoplasm. Predicted to be active in nucleus. Orthologous to human ATXN1L (ataxin 1 like).
PHENOTYPE: Mice homozygous for a null mutation display partial postnatal lethality with hydroencephaly, kyphosis, lethargy and cachexia. [provided by MGI curators]
  • synonyms:
  • ENSMUSG00000069895,
  • ataxin 1-like,
  • D8Ertd587e,
  • C330011L24Rik,
  • RIKEN cDNA C330011L24 gene,
  • MGI:3642562,
  • Boat,
  • DNA segment, Chr 8, ERATO Doi 587, expressed,
  • MGI:1261787,
  • predicted gene, ENSMUSG00000069895,
  • Atxn1l,
  • MGI:1926088

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For