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MINCR MYC-induced long non-coding RNA [ Homo sapiens (human) ]

Gene ID: 100507316, updated on 14-Dec-2021

Summary

Official Symbol
MINCRprovided by HGNC
Official Full Name
MYC-induced long non-coding RNAprovided by HGNC
Primary source
HGNC:HGNC:51653
See related
Ensembl:ENSG00000253716
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
LINC01604
Expression
Ubiquitous expression in fat (RPKM 4.1), thyroid (RPKM 2.9) and 25 other tissues See more
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Genomic context

See MINCR in Genome Data Viewer
Location:
8q24.3
Exon count:
3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 8 NC_000008.11 (143280155..143281700, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (144362325..144363870, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene ZFP41 zinc finger protein Neighboring gene GLI family zinc finger 4 Neighboring gene zinc finger protein 696 Neighboring gene DNA topoisomerase I mitochondrial Neighboring gene RNA, U6 small nuclear 220, 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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Other Names

  • MYC-induced long noncoding RNA
  • TCONS_00015189
  • long intergenic non-protein coding RNA 1604

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.

RNA

  1. NR_120682.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AA992445, AC138696, AW975318, HY339014, HY368981
    Related
    ENST00000517411.3
  2. NR_120683.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) differs in the 3' exon structure, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    AA284855, AJ346444, BM987389, HY368981

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p13 Primary Assembly

    Range
    143280155..143281700 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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