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LINC00482 long intergenic non-protein coding RNA 482 [ Homo sapiens (human) ]

Gene ID: 284185, updated on 13-May-2022

Summary

Official Symbol
LINC00482provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 482provided by HGNC
Primary source
HGNC:HGNC:26816
See related
AllianceGenome:HGNC:26816
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
C17orf55
Expression
Broad expression in spleen (RPKM 1.2), colon (RPKM 0.7) and 17 other tissues See more
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Genomic context

See LINC00482 in Genome Data Viewer
Location:
17q25.3
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (81302824..81309248, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (82214722..82221494, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (79276624..79283048, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904082 Neighboring gene CRISPRi-validated cis-regulatory element chr17.5937 Neighboring gene TMEM105 long non-coding RNA Neighboring gene basic proline-rich protein-like

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Clone Names

  • FLJ39421, MGC120553, MGC120556

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 

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_038080.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC027601, AK096740

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    81302824..81309248 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    82214722..82221494 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_178519.2: Suppressed sequence

    Description
    NM_178519.2: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.