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TRUND-NNN8-1 tRNA-undetermined (NNN) 8-1 [ Homo sapiens (human) ]

Gene ID: 103482528, updated on 13-May-2022

Summary

Official Symbol
TRUND-NNN8-1provided by HGNC
Official Full Name
tRNA-undetermined (NNN) 8-1provided by HGNC
Primary source
HGNC:HGNC:50820
See related
AllianceGenome:HGNC:50820
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
tRNA-Und-NNN-8-1
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Genomic context

See TRUND-NNN8-1 in Genome Data Viewer
Location:
1p13.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (107953653..107953723, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (107991131..107991201, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (108496275..108496345, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene NDUFA4 pseudogene 1 Neighboring gene vav guanine nucleotide exchange factor 3 Neighboring gene microRNA 7852 Neighboring gene Sharpr-MPRA regulatory region 13935 Neighboring gene VAV3 antisense RNA 1 Neighboring gene long intergenic non-protein coding RNA 2785

Genomic regions, transcripts, and products

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_034184.1 

    Range
    101..171
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    107953653..107953723 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    107991131..107991201 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)