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Protein Coding Gene : Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1
Primary Identifier  MGI:1332247 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  11416
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable acetyl-CoA transmembrane transporter activity and protein homodimerization activity. Predicted to be involved in acetyl-CoA transmembrane transport. Predicted to be located in endoplasmic reticulum membrane. Is expressed in several structures, including brain; heart; liver; metanephros; and spleen. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 42. Orthologous to human SLC33A1 (solute carrier family 33 member 1).
PHENOTYPE: Mice homozygous for a serine to arginine substitution at amino acid 113 show early embryonic growth arrest. Adult heterozygotes display aberrant inflammatory response, increased propensity to infections and malignancies, degenerative features of the PNS and CNS, and abnormal induction of autophagy. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA D630022N01 gene,
  • Acatn,
  • expressed sequence AI788741,
  • AI788741,
  • MGI:2442761,
  • solute carrier family 33 (acetyl-CoA transporter), member 1,
  • Slc33a1,
  • MGI:2139794,
  • expressed sequence AI315656,
  • MGI:2139668,
  • acetyl-Coenzyme A transporter,
  • D630022N01Rik,
  • AI315656
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Features --> Cross References

Genome

Sequence Feature Displayer

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2 Involved In Mutations

Trail: ProteinCodingGene

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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

3 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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