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    SULT1C3 sulfotransferase family 1C member 3 [ Homo sapiens (human) ]

    Gene ID: 442038, updated on 10-Dec-2024

    Summary

    Official Symbol
    SULT1C3provided by HGNC
    Official Full Name
    sulfotransferase family 1C member 3provided by HGNC
    Primary source
    HGNC:HGNC:33543
    See related
    Ensembl:ENSG00000196228 MIM:617151; AllianceGenome:HGNC:33543
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ST1C3
    Summary
    Enables 3'-phosphoadenosine 5'-phosphosulfate binding activity and sulfotransferase activity. Involved in 3'-phosphoadenosine 5'-phosphosulfate metabolic process; cholesterol metabolic process; and xenobiotic metabolic process. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Low expression observed in reference dataset See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See SULT1C3 in Genome Data Viewer
    Location:
    2q12.3
    Exon count:
    10
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (108239968..108265351)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (108700880..108726238)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (108856424..108881807)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1594 Neighboring gene SET domain containing 6 pseudogene 1 Neighboring gene WASF1 pseudogene 1 Neighboring gene sulfotransferase family 1C member 2

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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?

    Phenotypes

    EBI GWAS Catalog

    Description
    Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    sulfotransferase 1C3
    Names
    sulfotransferase family, cytosolic, 1C, member 3
    NP_001008743.1
    NP_001307807.1

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_001008743.3NP_001008743.1  sulfotransferase 1C3 isoform 2

      See identical proteins and their annotated locations for NP_001008743.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 3' UTR and coding sequence compared to variant 1. The resulting isoform (2) has a distinct C-terminus but is the same length as isoform 1.
      Source sequence(s)
      AC019100
      Consensus CDS
      CCDS33267.1
      UniProtKB/Swiss-Prot
      Q6IMI5, Q6IMI6
      Related
      ENSP00000333310.2, ENST00000329106.3
      Conserved Domains (1) summary
      pfam00685
      Location:46297
      Sulfotransfer_1; Sulfotransferase domain
    2. NM_001320878.2NP_001307807.1  sulfotransferase 1C3 isoform 1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1, coding) represents the allele encoded by the GRCh38 reference genome and encodes isoform (1).
      Source sequence(s)
      AC019100
      Consensus CDS
      CCDS92828.1
      UniProtKB/Swiss-Prot
      Q6IMI6
      Related
      ENSP00000505748.1, ENST00000681802.2
      Conserved Domains (1) summary
      pfam00685
      Location:46297
      Sulfotransfer_1; Sulfotransferase domain

    RNA

    1. NR_178047.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1, non-coding) uses the same exon combination as variant 1 but represents the allele present on the T2T-CHM13v2.0 genome assembly. This variant is represented as non-coding since the primary ORF has a stop codon >50 nucleotides from the terminal splice site; nonsense-mediated mRNA decay (NMD) candidate.
      Source sequence(s)
      CP068276

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      108239968..108265351
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      108700880..108726238
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)