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LINC00557 long intergenic non-protein coding RNA 557 [ Homo sapiens (human) ]

Gene ID: 100861544, updated on 12-Oct-2019

Summary

Official Symbol
LINC00557provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 557provided by HGNC
Primary source
HGNC:HGNC:43701
See related
Ensembl:ENSG00000260962
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See LINC00557 in Genome Data Viewer
Location:
13q32.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (94960041..94961319)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101927284 Neighboring gene ribosomal protein L21 pseudogene 112 Neighboring gene bromodomain containing 7 pseudogene 5 Neighboring gene VISTA enhancers hs189 and hs341 Neighboring gene RNA, U6 small nuclear 62, pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000013.11 Chromosome 13 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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_047487.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL139381
    Related
    ENST00000563184.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    94960041..94961319
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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