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    TUFMP1 Tu translation elongation factor, mitochondrial pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 645668, updated on 10-Oct-2023

    Summary

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    Official Symbol
    TUFMP1provided by HGNC
    Official Full Name
    Tu translation elongation factor, mitochondrial pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:12421
    See related
    Ensembl:ENSG00000265646 AllianceGenome:HGNC:12421
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TUFML
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    Genomic context

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    See TUFMP1 in Genome Data Viewer
    Location:
    17q11.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (27082492..27084123, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (28023131..28024762, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (25409518..25411149, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene general transcription factor IIi pseudogene 6 Neighboring gene uncharacterized LOC105371703 Neighboring gene vomeronasal 1 receptor 71 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11889 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11890 Neighboring gene uncharacterized LOC105371704 Neighboring gene uncharacterized LOC124903956 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11891

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus. Shah ZH, et al. Genomics, 1998 Mar 15. PMID 9545647

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    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.

    Genomic

    1. NG_006578.3 

      Range
      101..1732
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      27082492..27084123 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      28023131..28024762 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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