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LINC02894 long intergenic non-protein coding RNA 2894 [ Homo sapiens (human) ]

Gene ID: 100288748, updated on 25-Jan-2022

Summary

Official Symbol
LINC02894provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 2894provided by HGNC
Primary source
HGNC:HGNC:55364
See related
Ensembl:ENSG00000261437 AllianceGenome:HGNC:55364
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

See LINC02894 in Genome Data Viewer
Location:
8q22.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 8 NC_000008.11 (94637285..94639467, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (95649513..95651695, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene vir like m6A methyltransferase associated Neighboring gene ribosomal protein L31 pseudogene Neighboring gene VIRMA divergent transcript Neighboring gene epithelial splicing regulatory protein 1 Neighboring gene ribosomal protein S15a pseudogene 26 Neighboring gene dpy-19 like 4

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_034034.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC108860, AK057998
    Related
    ENST00000562760.1

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_000008.11 Reference GRCh38.p13 Primary Assembly

    Range
    94637285..94639467 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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