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    SULT1A3 sulfotransferase family 1A member 3 [ Homo sapiens (human) ]

    Gene ID: 6818, updated on 14-Nov-2024

    Summary

    Official Symbol
    SULT1A3provided by HGNC
    Official Full Name
    sulfotransferase family 1A member 3provided by HGNC
    Primary source
    HGNC:HGNC:11455
    See related
    Ensembl:ENSG00000261052 MIM:600641; AllianceGenome:HGNC:11455
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    STM; HAST; HAST3; M-PST; ST1A3; ST1A4; ST1A5; TL-PST; ST1A3/ST1A4
    Summary
    Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a phenol sulfotransferase with thermolabile enzyme activity. Four sulfotransferase genes are located on the p arm of chromosome 16; this gene and SULT1A4 arose from a segmental duplication. This gene is the most centromeric of the four sulfotransferase genes. Read-through transcription exists between this gene and the upstream SLX1A (SLX1 structure-specific endonuclease subunit homolog A) gene that encodes a protein containing GIY-YIG domains. [provided by RefSeq, Nov 2010]
    Expression
    Broad expression in duodenum (RPKM 134.6), small intestine (RPKM 93.8) and 23 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See SULT1A3 in Genome Data Viewer
    Location:
    16p11.2
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (30199255..30204310)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (30483809..30488863)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (30210576..30215631)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr16:30204716-30205440 Neighboring gene SLX1A-SULT1A3 readthrough (NMD candidate) Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:30206166-30206889 Neighboring gene bolA family member 2B Neighboring gene SLX1 homolog A, structure-specific endonuclease subunit Neighboring gene SAGA complex associated factor 29 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:30218380-30219378 Neighboring gene uncharacterized LOC101929894 Neighboring gene phospholipase A2 group XJ, pseudogene

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Readthrough SLX1A-SULT1A3

    Readthrough gene: SLX1A-SULT1A3, Included gene: SLX1A

    Clone Names

    • MGC117469

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables amine sulfotransferase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables aryl sulfotransferase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables aryl sulfotransferase activity IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables sulfate binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables sulfotransferase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in 3'-phosphoadenosine 5'-phosphosulfate metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in cellular response to dopamine IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in dopamine catabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in dopamine metabolic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in ethanol catabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in flavonoid metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in steroid metabolic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in sulfation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in sulfation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in xenobiotic metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytosol TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    sulfotransferase 1A3
    Names
    Sulfotransferase 1A4
    aryl sulfotransferase 1A3/1A4
    catecholamine-sulfating phenol sulfotransferase
    dopamine-specific sulfotransferase
    monoamine-sulfating phenosulfotransferase
    phenol sulfotransferase 1A5
    placental estrogen sulfotransferase
    sulfokinase
    sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3
    thermolabile (monoamine, M form) phenol sulfotransferase
    NP_808220.1

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_177552.4NP_808220.1  sulfotransferase 1A3

      See identical proteins and their annotated locations for NP_808220.1

      Status: REVIEWED

      Source sequence(s)
      BC078144, BC144355
      Consensus CDS
      CCDS10674.1
      UniProtKB/Swiss-Prot
      B4DNV0, O95603, P0DMM9, P0DMN0, P50224, Q1ET66, Q6ZWJ5
      UniProtKB/TrEMBL
      B3KT14, Q1ET61, Q1ET62, Q1ET63, Q2TAB3
      Related
      ENSP00000343645.6, ENST00000338971.10
      Conserved Domains (1) summary
      pfam00685
      Location:38287
      Sulfotransfer_1; Sulfotransferase domain

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      30199255..30204310
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      30483809..30488863
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001017387.1: Suppressed sequence

      Description
      NM_001017387.1: This RefSeq was permanently suppressed because currently there is not sufficient data to support this transcript.
    2. NM_003166.3: Suppressed sequence

      Description
      NM_003166.3: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.