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RNU6-279P RNA, U6 small nuclear 279, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479690, updated on 23-Nov-2021

Summary

Official Symbol
RNU6-279Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 279, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47242
See related
Ensembl:ENSG00000212599
Gene type
pseudo
RefSeq status
INFERRED
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 RNU6-279P in Genome Data Viewer
Location:
12q14.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (59369051..59369151, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (59762832..59762932, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene LRIG3 divergent transcript Neighboring gene VISTA enhancer hs1427 Neighboring gene methyltransferase like 15 pseudogene 2 Neighboring gene RNA, U6 small nuclear 871, pseudogene Neighboring gene long intergenic non-protein coding RNA 2448

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.

Genomic

  1. NG_043513.1 

    Range
    101..201
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    59369051..59369151 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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