U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

NDUFV1-DT NDUFV1 divergent transcript [ Homo sapiens (human) ]

Gene ID: 100505621, updated on 13-May-2022

Summary

Official Symbol
NDUFV1-DTprovided by HGNC
Official Full Name
NDUFV1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:26915
See related
Ensembl:ENSG00000184224 AllianceGenome:HGNC:26915
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C11orf72
Expression
Low expression observed in reference dataset See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See NDUFV1-DT in Genome Data Viewer
Location:
11q13.2
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (67602880..67606706, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (67597568..67601394, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (67370351..67374177, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene calcium binding protein 2 Neighboring gene glutathione S-transferase pi 1 Neighboring gene NADH:ubiquinone oxidoreductase core subunit V1 Neighboring gene double C2 domain gamma, pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Clone Names

  • FLJ90834, MGC129824, MGC129825

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

RNA

  1. NR_130935.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP003385
    Related
    ENST00000333139.3

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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    67602880..67606706 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    67597568..67601394 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_173578.1: Suppressed sequence

    Description
    NM_173578.1: This RefSeq was permanently suppressed because it is mostly repetitive sequence.