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Protein Coding Gene : Sult4a1 sulfotransferase family 4A, member 1
Primary Identifier  MGI:1888971 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  29859
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables sulfotransferase activity. Acts upstream of or within sulfur compound metabolic process. Located in cytosol and mitochondrion. Is expressed in embryo. Orthologous to human SULT4A1 (sulfotransferase family 4A member 1).
PHENOTYPE: Mice homozygous for a null allele exhibit progressive tremors, ataxia, abnormal gait, absence seizure, porstnatal growth retardation and premature death. [provided by MGI curators]
  • synonyms:
  • Sult4a1,
  • sulfotransferase family 4A, member 1,
  • AI853543,
  • 2400007A17Rik,
  • RIKEN cDNA 2400007A17 gene,
  • MGI:2146093,
  • expressed sequence AI853543,
  • MGI:1914231,
  • Sultx3,
  • BR-STL-1
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Genome

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3 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

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Function

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Homology

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Interactions

4 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

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