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LINC02986 long intergenic non-protein coding RNA 2986 [ Homo sapiens (human) ]

Gene ID: 123689089, updated on 10-Oct-2023

Summary

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Official Symbol
LINC02986provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2986provided by HGNC
Primary source
HGNC:HGNC:56083
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
8q21.13
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (80539647..80543099)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (80971233..80974685)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375921 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27568 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:81398027-81398597 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:81398598-81399168 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19324 Neighboring gene zinc finger and BTB domain containing 10 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81415452-81415952 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:81470238-81471437 Neighboring gene RNA, U7 small nuclear 174 pseudogene Neighboring gene ribosomal protein SA pseudogene 47

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

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_186600.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009812

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    80539647..80543099
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    80971233..80974685
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases