Format

Send to:

Choose Destination

RNU6-878P RNA, U6 small nuclear 878, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479954, updated on 1-Aug-2020

Summary

Official Symbol
RNU6-878Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 878, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47841
See related
Ensembl:ENSG00000207308
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RNU6-878P in Genome Data Viewer
Location:
11p15.5
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (2321718..2321827)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene achaete-scute family bHLH transcription factor 2 Neighboring gene chromosome 11 open reading frame 21 Neighboring gene tetraspanin 32 Neighboring gene CD81 antisense RNA 1 Neighboring gene ribosomal protein L26 pseudogene 30 Neighboring gene uncharacterized LOC105376520

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000011.10 Chromosome 11 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.

Genomic

  1. NG_043582.1 

    Range
    101..210
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    2321718..2321827
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center