Atl1 - atlastin GTPase 1 Gene

Also Known as Fsp1; Spg3; Adfsp; Spg3a; 4930435M24Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 73991

Summary

This gene encodes a member of the Dynamin family of GTPases. The encoded protein interacts with tubule-shaping proteins of the endoplasmic reticulum. Mutations in the homologous human gene can cause hereditary spastic paraplegia. [provided by RefSeq, Feb 2010]

Atl1 Products (1)

mRNA Protein Name
NM_178628.5 NP_848743.1 atlastin-1

Gene Ontology

  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
24668814 MGI
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
22984613 MGI
located in endoplasmic reticulum tubular network IDA
IDA: Inferred from direct assay
24668814 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

atlastin-1

  • spastic paraplegia 3A homolog

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (4)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS01157 ATL1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS01414 BCL11B Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS19876 Atl1 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS26375 Atl1 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Atl1 NCBI NCBI:51062