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SULT6B1 sulfotransferase family 6B member 1 [ Homo sapiens (human) ]

Gene ID: 391365, updated on 23-Nov-2021

Summary

Official Symbol
SULT6B1provided by HGNC
Official Full Name
sulfotransferase family 6B member 1provided by HGNC
Primary source
HGNC:HGNC:33433
See related
Ensembl:ENSG00000138068 MIM:617152
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
ST6B1
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See SULT6B1 in Genome Data Viewer
Location:
2p22.2
Exon count:
9
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (37167820..37196087, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (37394963..37423230, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene G-patch domain containing 11 Neighboring gene eukaryotic translation initiation factor 2 alpha kinase 2 Neighboring gene ARL14EP pseudogene 1 Neighboring gene ribosomal protein L31 pseudogene 16 Neighboring gene CEBPZ opposite strand Neighboring gene CCAAT enhancer binding protein zeta Neighboring gene NADH:ubiquinone oxidoreductase complex assembly factor 7 Neighboring gene protein kinase D3

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

Phenotypes

Associated conditions

Description Tests
Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
GeneReviews: Not available

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables sulfotransferase activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
involved_in sulfation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
located_in cytosol TAS
Traceable Author Statement
more info
 

General protein information

Preferred Names
sulfotransferase 6B1
Names
sulfotransferase SULT6B1
sulfotransferase family, cytosolic, 6B, member 1
thyroxine sulfotransferase
NP_001027549.1
NP_001354480.1

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_001032377.2NP_001027549.1  sulfotransferase 6B1 isoform 2

    See identical proteins and their annotated locations for NP_001027549.1

    Status: VALIDATED

    Source sequence(s)
    AC007390, AC007899
    Consensus CDS
    CCDS33182.1
    UniProtKB/Swiss-Prot
    Q6IMI4
    UniProtKB/TrEMBL
    A0A0C4DG03
    Conserved Domains (1) summary
    pfam00685
    Location:18251
    Sulfotransfer_1; Sulfotransferase domain
  2. NM_001367551.1NP_001354480.1  sulfotransferase 6B1 isoform 1

    Status: VALIDATED

    Source sequence(s)
    AC007899
    Related
    ENSP00000444081.1, ENST00000535679.6

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    37167820..37196087 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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