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LINC02983 long intergenic non-protein coding RNA 2983 [ Homo sapiens (human) ]

Gene ID: 100129484, updated on 14-Dec-2021

Summary

Official Symbol
LINC02983provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2983provided by HGNC
Primary source
HGNC:HGNC:56060
See related
Ensembl:ENSG00000234432
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
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Genomic context

See LINC02983 in Genome Data Viewer
Location:
7p22.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (5426277..5428927, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (5465912..5468387, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 13937 Neighboring gene solute carrier family 29 member 4 Neighboring gene trinucleotide repeat containing 18 Neighboring gene F-box and leucine rich repeat protein 18 Neighboring gene microRNA 589 Neighboring gene uncharacterized LOC221946

Genomic regions, transcripts, and products

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_171035.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC092171
    Related
    ENST00000610122.1

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_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    5426277..5428927 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001354886.2: Suppressed sequence

    Description
    NM_001354886.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.
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