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    ORT1 Ort1p [ Saccharomyces cerevisiae S288C ]

    Gene ID: 854297, updated on 9-Dec-2024

    Summary

    Official Symbol
    ORT1
    Official Full Name
    Ort1p
    Primary source
    SGD:S000005656
    Locus tag
    YOR130C
    See related
    AllianceGenome:SGD:S000005656; FungiDB:YOR130C; VEuPathDB:YOR130C
    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
    ARG11
    Summary
    Enables L-ornithine transmembrane transporter activity. Involved in L-arginine biosynthetic process and mitochondrial L-ornithine transmembrane transport. Located in mitochondrial envelope. Used to study ornithine translocase deficiency. Human ortholog(s) of this gene implicated in amino acid metabolic disorder; citrullinemia; and ornithine translocase deficiency. Orthologous to human SLC25A15 (solute carrier family 25 member 15) and SLC25A2 (solute carrier family 25 member 2). [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See ORT1 in Genome Data Viewer
    Location:
    chromosome: XV
    Exon count:
    1
    Sequence:
    Chromosome: XV; NC_001147.6 (569929..570807, complement)

    Chromosome XV - NC_001147.6Genomic Context describing neighboring genes Neighboring gene phosphoribosylaminoimidazole carboxylase ADE2 Neighboring gene Afi1p Neighboring gene tRNA-Asp Neighboring gene putative haloacid dehalogenase-like hydrolase

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    Ort1p
    NP_014773.4
    • Ornithine transporter of the mitochondrial inner membrane; exports ornithine from mitochondria as part of arginine biosynthesis; functionally complemented by human ortholog, SLC25A15, which is associated with hyperammonaemia-hyperornithinaemia-homocitrullinuria (HHH) syndrome, but HHH-associated variants fail to complement

    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_001147.6 Reference assembly

      Range
      569929..570807 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001183549.4NP_014773.4  TPA: Ort1p [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_014773.4

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6W2I8, Q12375, Q92273
      UniProtKB/TrEMBL
      A6ZNX7, B3LJH2, B5VS20, C7GMK9, C8ZI92, G2WN05, N1NYG4
      Conserved Domains (1) summary
      pfam00153
      Location:103200
      Mito_carr; Mitochondrial carrier protein