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LINC02897 long intergenic non-protein coding RNA 2897 [ Homo sapiens (human) ]

Gene ID: 388759, updated on 23-Nov-2021

Summary

Official Symbol
LINC02897provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2897provided by HGNC
Primary source
HGNC:HGNC:33759
See related
Ensembl:ENSG00000221953
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
C1orf229
Orthologs
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Genomic context

See LINC02897 in Genome Data Viewer
Location:
1q44
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (247110155..247112417, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (247273457..247275719, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 11854 Neighboring gene zinc finger protein 669 Neighboring gene uncharacterized LOC400812 Neighboring gene fibroblast growth factor receptor 3 pseudogene 6 Neighboring gene zinc finger protein 124

Genomic regions, transcripts, and products

General gene information

Markers

Homology

Clone Names

  • FLJ45717

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_167894.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL390728
    Related
    ENST00000623686.1

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_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    247110155..247112417 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_207401.2: Suppressed sequence

    Description
    NM_207401.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.
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