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    HNM1 Hnm1p [ Saccharomyces cerevisiae S288C ]

    Gene ID: 852803, updated on 9-Dec-2024

    Summary

    Official Symbol
    HNM1
    Official Full Name
    Hnm1p
    Primary source
    SGD:S000003045
    Locus tag
    YGL077C
    See related
    AllianceGenome:SGD:S000003045; FungiDB:YGL077C; VEuPathDB:YGL077C
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Saccharomyces cerevisiae S288C (strain: S288C)
    Lineage
    Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
    Also known as
    CTR1
    Summary
    Enables (R)-carnitine transmembrane transporter activity; choline transmembrane transporter activity; and ethanolamine transmembrane transporter activity. Involved in amino-acid betaine transport; choline transport; and ethanolamine transport. Located in cell periphery and endoplasmic reticulum. Used to study proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome. [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See HNM1 in Genome Data Viewer
    Location:
    chromosome: VII
    Exon count:
    1
    Sequence:
    Chromosome: VII; NC_001139.9 (362225..363916, complement)

    Chromosome VII - NC_001139.9Genomic Context describing neighboring genes Neighboring gene Kxd1p Neighboring gene RNA-dependent ATPase DBP3 Neighboring gene ribosomal 60S subunit protein L7A Neighboring gene ncRNA Neighboring gene ncRNA

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by SGD

    Process Evidence Code Pubs
    involved_in (R)-carnitine transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in (R)-carnitine transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in amino acid transport IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in choline transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in ethanolamine transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in gamma-aminobutyric acid transport IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in glycine betaine transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    Hnm1p
    NP_011438.1
    • Plasma membrane transporter for choline, ethanolamine, and carnitine; involved in the uptake of nitrogen mustard and the uptake of glycine betaine during hypersaline stress; co-regulated with phospholipid biosynthetic genes and negatively regulated by choline and myo-inositol; human FLVCR2 (MFSD7c), a choline transporter involved in Fowler syndrome, can complement the yeast null mutant

    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
      362225..363916 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001180942.1NP_011438.1  TPA: Hnm1p [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_011438.1

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6VU67, P19807
      UniProtKB/TrEMBL
      A6ZUA2, B3LHE3, C7GW38, C8Z8H0, G2WE22, N1P9Q6
      Conserved Domains (1) summary
      TIGR00907
      Location:45521
      2A0304; amino acid permease (GABA permease)