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    HS3ST3B1 heparan sulfate-glucosamine 3-sulfotransferase 3B1 [ Homo sapiens (human) ]

    Gene ID: 9953, updated on 10-Dec-2024

    Summary

    Official Symbol
    HS3ST3B1provided by HGNC
    Official Full Name
    heparan sulfate-glucosamine 3-sulfotransferase 3B1provided by HGNC
    Primary source
    HGNC:HGNC:5198
    See related
    Ensembl:ENSG00000125430 MIM:604058; AllianceGenome:HGNC:5198
    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
    3OST3B1; 3-OST-3B; h3-OST-3B
    Summary
    The protein encoded by this gene is a type II integral membrane protein that belongs to the 3-O-sulfotransferases family. These proteins catalyze the addition of sulfate groups at the 3-OH position of glucosamine in heparan sulfate. The substrate specificity of individual members of the family is based on prior modification of the heparan sulfate chain, thus allowing different members of the family to generate binding sites for different proteins on the same heparan sulfate chain. Following treatment with a histone deacetylase inhibitor, expression of this gene is activated in a pancreatic cell line. The increased expression results in promotion of the epithelial-mesenchymal transition. In addition, the modification catalyzed by this protein allows herpes simplex virus membrane fusion and penetration. A very closely related homolog with an almost identical sulfotransferase domain maps less than 1 Mb away. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
    Expression
    Broad expression in liver (RPKM 6.8), lymph node (RPKM 3.1) and 21 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See HS3ST3B1 in Genome Data Viewer
    Location:
    17p12
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (14301081..14349404)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (14207195..14255584)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (14204398..14252721)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11742 Neighboring gene cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 Neighboring gene distal CMT1A-REP Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_47071 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:14109359-14109859 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:14139403-14139910 Neighboring gene CMT1A duplicated region transcript 15 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8208 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:14206998-14207498 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8209 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:14213102-14213622 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:14213623-14214143 Neighboring gene NANOG hESC enhancer GRCh37_chr17:14226810-14227361 Neighboring gene uncharacterized protein MGC12916 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:14256381-14257207 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 8210 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:14276639-14277838 Neighboring gene uncharacterized LOC107985080 Neighboring gene NANOG hESC enhancer GRCh37_chr17:14462906-14463439 Neighboring gene uncharacterized LOC107984996

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association study identifies protein quantitative trait loci (pQTLs).
    EBI GWAS Catalog
    Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    heparan sulfate glucosamine 3-O-sulfotransferase 3B1
    Names
    heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1
    heparan sulfate 3-O-sulfotransferase 3B1
    heparan sulfate D-glucosaminyl 3-O-sulfotransferase 3B1
    NP_006032.1
    XP_016880968.1

    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_006041.3NP_006032.1  heparan sulfate glucosamine 3-O-sulfotransferase 3B1

      See identical proteins and their annotated locations for NP_006032.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longer transcript. It encodes the protein.
      Source sequence(s)
      AC005224, AK023723, BC063301, BM968044, DA388077
      Consensus CDS
      CCDS11167.1
      UniProtKB/Swiss-Prot
      B3KN58, D3DTS6, Q9Y662
      Related
      ENSP00000354213.2, ENST00000360954.3
      Conserved Domains (1) summary
      pfam00685
      Location:137374
      Sulfotransfer_1; Sulfotransferase domain

    RNA

    1. NR_130138.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate 3' exon structure compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AC005224, AC022816, AK023723, BC063301, BM968044, DA388077

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      14301081..14349404
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_017025479.3XP_016880968.1  heparan sulfate glucosamine 3-O-sulfotransferase 3B1 isoform X1

      UniProtKB/TrEMBL
      J3KSX5

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      14207195..14255584
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)