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    VHT1 Vht1p [ Saccharomyces cerevisiae S288C ]

    Gene ID: 852956, updated on 9-Dec-2024

    Summary

    Official Symbol
    VHT1
    Official Full Name
    Vht1p
    Primary source
    SGD:S000003297
    Locus tag
    YGR065C
    See related
    AllianceGenome:SGD:S000003297; FungiDB:YGR065C; VEuPathDB:YGR065C
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Saccharomyces cerevisiae S288C (strain: S288C)
    Lineage
    Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
    Summary
    Enables biotin transmembrane transporter activity. Involved in biotin transport. Located in plasma membrane. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 25; gout; porokeratosis; and sialuria. Orthologous to several human genes including SLC17A1 (solute carrier family 17 member 1); SLC17A2 (solute carrier family 17 member 2); and SLC17A3 (solute carrier family 17 member 3). [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See VHT1 in Genome Data Viewer
    Location:
    chromosome: VII
    Exon count:
    1
    Sequence:
    Chromosome: VII; NC_001139.9 (618077..619858, complement)

    Chromosome VII - NC_001139.9Genomic Context describing neighboring genes Neighboring gene membrane insertase COX18 Neighboring gene transcription elongation factor SPT4 Neighboring gene Gid10p Neighboring gene uncharacterized protein

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by SGD

    Function Evidence Code Pubs
    enables biotin transmembrane transporter activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables symporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables transmembrane transporter activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables transmembrane transporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in biotin transport IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in cell periphery HDA PubMed 
    is_active_in membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    Vht1p
    NP_011579.1
    • High-affinity plasma membrane H+-biotin (vitamin H) symporter; mutation results in fatty acid auxotrophy; 12 transmembrane domain containing major facilitator subfamily member; mRNA levels negatively regulated by iron deprivation and biotin

    NCBI Reference Sequences (RefSeq)

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    Genome Annotation

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

    Reference assembly

    Genomic

    1. NC_001139.9 Reference assembly

      Range
      618077..619858 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001181194.1NP_011579.1  TPA: Vht1p [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_011579.1

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6VUJ9, P53241
      UniProtKB/TrEMBL
      A6ZV49, B3LIF9, C7GXP7, N1P3I8
      Conserved Domains (1) summary
      cd17327
      Location:124542
      MFS_FEN2_like; Pantothenate transporter FEN2 and similar transporters of the Major Facilitator Superfamily