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    NMTRQ-CTG1-1 nuclear-encoded mitochondrial tRNA-Gln (CTG) 1-1 [ Homo sapiens (human) ]

    Gene ID: 100189461, updated on 10-Dec-2024

    Summary

    Official Symbol
    NMTRQ-CTG1-1provided by HGNC
    Official Full Name
    nuclear-encoded mitochondrial tRNA-Gln (CTG) 1-1provided by HGNC
    Primary source
    HGNC:HGNC:35033
    See related
    AllianceGenome:HGNC:35033
    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
    TRNAQ38P
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    Genomic context

    See NMTRQ-CTG1-1 in Genome Data Viewer
    Location:
    10p12.31
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (19747679..19747753, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (19765936..19766010, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (20036608..20036682, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene MAM and LDL receptor class A domain containing 1 Neighboring gene uncharacterized LOC101928834 Neighboring gene Sharpr-MPRA regulatory region 1632 Neighboring gene MPRA-validated peak895 silencer Neighboring gene MT-ND1 pseudogene 37 Neighboring gene MT-ND2 pseudogene 16 Neighboring gene RNA, U6 small nuclear 1212, pseudogene

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • nmt-tRNA-Gln-CTG-1-1
    • nuclear-encoded mitochondrial transfer RNA-Gln (CTG) 1-1
    • transfer RNA glutamine 38 (anticodon CUG) pseudogene

    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_008518.1 

      Range
      101..175
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      19747679..19747753 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      19765936..19766010 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)