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    TIM8 protein transporter TIM8 [ Saccharomyces cerevisiae S288C ]

    Gene ID: 853600, updated on 9-Dec-2024

    Summary

    Official Symbol
    TIM8
    Official Full Name
    protein transporter TIM8
    Primary source
    SGD:S000007348
    Locus tag
    YJR135W-A
    See related
    AllianceGenome:SGD:S000007348; FungiDB:YJR135W-A; VEuPathDB:YJR135W-A
    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 protein transporter activity. Involved in protein insertion into mitochondrial inner membrane. Located in mitochondrion. Part of mitochondrial intermembrane space protein transporter complex. Used to study deafness-dystonia-optic neuronopathy syndrome. Human ortholog(s) of this gene implicated in deafness-dystonia-optic neuronopathy syndrome and dystonia. Orthologous to human TIMM8B (translocase of inner mitochondrial membrane 8 homolog B) and TIMM8A (translocase of inner mitochondrial membrane 8A). [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See TIM8 in Genome Data Viewer
    Location:
    chromosome: X
    Exon count:
    1
    Sequence:
    Chromosome: X; NC_001142.9 (676971..677234)

    Chromosome X - NC_001142.9Genomic Context describing neighboring genes Neighboring gene Sgm1p Neighboring gene Mcm22p Neighboring gene Tti2p Neighboring gene sulfite reductase (NADPH) subunit beta

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    General protein information

    Preferred Names
    protein transporter TIM8
    NP_058168.1
    • Mitochondrial intermembrane space protein; forms a complex with Tim13p that delivers a subset of hydrophobic proteins to the TIM22 complex for inner membrane insertion; homolog of human TIMM8A, implicated in Mohr-Tranebjaerg syndrome, also known as deafness-dystonia-optic neuronopathy (DDON) syndrome; human TIMM8A can complement 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_001142.9 Reference assembly

      Range
      676971..677234
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001184382.1NP_058168.1  TPA: protein transporter TIM8 [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_058168.1

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6VWV4, P57744
      UniProtKB/TrEMBL
      A6ZQ91, B3LQL8, C7GM77, C8ZBT4, G2WHD8, N1P3Q3
      Conserved Domains (1) summary
      pfam02953
      Location:2383
      zf-Tim10_DDP; Tim10/DDP family zinc finger