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NMTRQ-TTG13-1 nuclear-encoded mitochondrial tRNA-Gln (TTG) 13-1 [ Homo sapiens (human) ]

Gene ID: 100189535, updated on 17-Sep-2024

Summary

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Official Symbol
NMTRQ-TTG13-1provided by HGNC
Official Full Name
nuclear-encoded mitochondrial tRNA-Gln (TTG) 13-1provided by HGNC
Primary source
HGNC:HGNC:35112
See related
AllianceGenome:HGNC:35112
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
TRNAQ52P
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Genomic context

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See NMTRQ-TTG13-1 in Genome Data Viewer
Location:
7p11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (57186273..57186344, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (57429562..57429633, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (57253980..57254051, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene GUSB pseudogene 10 Neighboring gene MT-CYB pseudogene 29 Neighboring gene MT-ND1 pseudogene 4 Neighboring gene MT-ND2 pseudogene 6 Neighboring gene MT-CO1 pseudogene 10 Neighboring gene MT-CO2 pseudogene 10

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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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Other Names

  • nmt-tRNA-Gln-TTG-13-1
  • nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 13-1
  • transfer RNA glutamine 52 (anticodon UUG) pseudogene
  • transfer RNA-Gln (TTG) 13-1

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_008593.1 

    Range
    101..172
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    57186273..57186344 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    57429562..57429633 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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