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NQO1-DT NQO1 divergent transcript [ Homo sapiens (human) ]

Gene ID: 119139903, updated on 8-Dec-2022

Summary

Official Symbol
NQO1-DTprovided by HGNC
Official Full Name
NQO1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:55344
Gene type
ncRNA
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FASRL
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Genomic context

See NQO1-DT in Genome Data Viewer
Location:
16q22.1
Exon count:
2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (69727015..69731571)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA, C/D box 13H Neighboring gene NAD(P)H quinone dehydrogenase 1 Neighboring gene NIN1 (RPN12) binding protein 1 homolog Neighboring gene non-POU domain containing, octamer-binding pseudogene 1

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000016.10 Chromosome 16 Reference GRCh38.p14 Primary Assembly

NCBI Reference Sequences (RefSeq)

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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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    69727015..69731571
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007065098.1 RNA Sequence