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LINC01667 long intergenic non-protein coding RNA 1667 [ Homo sapiens (human) ]

Gene ID: 441058, updated on 10-Oct-2023

Summary

Official Symbol
LINC01667provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1667provided by HGNC
Primary source
HGNC:HGNC:52455
See related
AllianceGenome:HGNC:52455
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Restricted expression toward testis (RPKM 4.6) See more
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Genomic context

See LINC01667 in Genome Data Viewer
Location:
21p11.2
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (9781848..9821061, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (9347362..9386594, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 Unlocalized Scaffold NT_113885.1 (49162..88375, complement)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379514 Neighboring gene uncharacterized LOC124904997 Neighboring gene MPRA-validated peak4340 silencer Neighboring gene uncharacterized LOC124900471 Neighboring gene RNA, 7SL, cytoplasmic 52, 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

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_038377.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC018692, AW303457, BC029568

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    9781848..9821061 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    9347362..9386594 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001004347.1: Suppressed sequence

    Description
    NM_001004347.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.