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    STX6 syntaxin 6 [ Homo sapiens (human) ]

    Gene ID: 10228, updated on 3-Nov-2024

    Summary

    Official Symbol
    STX6provided by HGNC
    Official Full Name
    syntaxin 6provided by HGNC
    Primary source
    HGNC:HGNC:11441
    See related
    Ensembl:ENSG00000135823 MIM:603944; AllianceGenome:HGNC:11441
    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
    Summary
    Enables syntaxin binding activity. Involved in regulation of protein localization; retrograde transport, endosome to Golgi; and vesicle fusion. Acts upstream of or within endocytic recycling. Located in several cellular components, including early endosome; perinuclear region of cytoplasm; and trans-Golgi network. Part of SNARE complex. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Ubiquitous expression in brain (RPKM 10.0), esophagus (RPKM 7.6) and 24 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See STX6 in Genome Data Viewer
    Location:
    1q25.3
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (180972725..181022870, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (180327972..180378137, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (180941861..180992006, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene KIAA1614 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:180918561-180919111 Neighboring gene KIAA1614 antisense RNA 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1597 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:180923653-180924258 Neighboring gene major histocompatibility complex, class I-related pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1598 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:180959945-180960105 Neighboring gene MPRA-validated peak491 silencer Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:180991746-180992529 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2167 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2166 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2168 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2169 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2170 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:181014030-181014179 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:181015297-181015799 Neighboring gene major histocompatibility complex, class I-related Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2171 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2172 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:181046610-181047144 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:181047145-181047678 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1601 Neighboring gene uncharacterized LOC124904465 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1602

    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?

    Phenotypes

    EBI GWAS Catalog

    Description
    Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Nef nef Genome-wide shRNA screening identifies STX6, which is required for HIV-1 Nef-induced downregulation of CD4 in HeLa CD4+ cells PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    General gene information

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables SNAP receptor activity  
    enables SNARE binding  
    enables protein binding PubMed 
    enables syntaxin binding PubMed 
    Process Evidence Code Pubs
    involved_in Golgi vesicle transport  
    acts_upstream_of_or_within endocytic recycling PubMed 
    involved_in endocytic recycling PubMed 
    involved_in endocytic recycling  
    involved_in intracellular protein transport  
    involved_in regulation of protein localization PubMed 
    involved_in retrograde transport, endosome to Golgi  
    involved_in retrograde transport, endosome to Golgi PubMed 
    involved_in retrograde transport, endosome to Golgi  
    involved_in synaptic vesicle to endosome fusion  
    involved_in vesicle docking  
    involved_in vesicle fusion  
    involved_in vesicle fusion PubMed 
    Component Evidence Code Pubs
    located_in Golgi apparatus PubMed 
    located_in Golgi membrane  
    part_of SNARE complex  
    part_of SNARE complex PubMed 
    located_in clathrin-coated vesicle PubMed 
    located_in cytosol  
    located_in early endosome PubMed 
    is_active_in endomembrane system  
    located_in nucleoplasm  
    located_in perinuclear region of cytoplasm PubMed 
    located_in phagocytic vesicle  
    located_in plasma membrane PubMed 
    located_in recycling endosome  
    located_in recycling endosome membrane  
    is_active_in synaptic vesicle membrane  
    located_in trans-Golgi network PubMed 
    located_in trans-Golgi network membrane  
    located_in trans-Golgi network membrane  

    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_001286210.2NP_001273139.1  syntaxin-6 isoform 2

      See identical proteins and their annotated locations for NP_001273139.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and lacks a portion of the 5' coding region and uses a downstream start codon, compared to variant 1. The encoded isoform (2) has a shorter N-terminus compared to isoform (1).
      Source sequence(s)
      AK299063, AL162431, AL356267
      Consensus CDS
      CCDS65738.1
      UniProtKB/Swiss-Prot
      O43752
      Related
      ENSP00000440188.1, ENST00000542060.5
      Conserved Domains (1) summary
      cd15851
      Location:65130
      SNARE_Syntaxin6; SNARE motif of syntaxin 6
    2. NM_005819.6NP_005810.1  syntaxin-6 isoform 1

      See identical proteins and their annotated locations for NP_005810.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
      Source sequence(s)
      AL162431, BC009944, DA311923
      Consensus CDS
      CCDS1341.1
      UniProtKB/Swiss-Prot
      B2R652, B4DR17, O43752, Q5VY08, Q6FH83
      Related
      ENSP00000258301.5, ENST00000258301.6
      Conserved Domains (2) summary
      cd15851
      Location:166231
      SNARE_Syntaxin6; SNARE motif of syntaxin 6
      cd21447
      Location:5107
      SNARE_NTD_STX6; N-terminal domain of syntaxin-6

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      180972725..181022870 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      180327972..180378137 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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