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NRON non-protein coding RNA, repressor of NFAT [ Homo sapiens (human) ]

Gene ID: 641373, updated on 5-Jul-2015
Official Symbol
NRONprovided by HGNC
Official Full Name
non-protein coding RNA, repressor of NFATprovided by HGNC
Primary source
HGNC:HGNC:37079
See related
MIM:609618
Gene type
ncRNA
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NCRNA00194
Orthologs
See NRON in Epigenomics, MapViewer
Location:
9q33.3; 9
Exon count:
1
Annotation release Status Assembly Chr Location
107 current GRCh38.p2 (GCF_000001405.28) 9 NC_000009.12 (126407775..126410504, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (129170054..129172783, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376275 Neighboring gene uncharacterized LOC101929116 Neighboring gene multivesicular body subunit 12B Neighboring gene uncharacterized LOC105376276 Neighboring gene uncharacterized LOC105376277

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Products Interactant Other Gene Complex Source Pubs Description

Homology

Other Names

  • noncoding repressor of NFAT

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_045006.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC006443

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 107

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

Reference GRCh38.p2 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p2 Primary Assembly

    Range
    126407775..126410504
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018920.2 Alternate CHM1_1.1

    Range
    129321083..129323807
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)