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RNU6-847P RNA, U6 small nuclear 847, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481448, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-847Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 847, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47810
See related
Ensembl:ENSG00000223047 AllianceGenome:HGNC:47810
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

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See RNU6-847P in Genome Data Viewer
Location:
10p11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (34926775..34926882)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (34955301..34955408)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (35215703..35215810)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene PARD3 divergent transcript Neighboring gene SS18 like 2 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:35207011-35207678 Neighboring gene MPRA-validated peak927 silencer Neighboring gene RNA, U6 small nuclear 193, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:35247828-35248328 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:35248329-35248829 Neighboring gene peroxiredoxin 2 pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_043244.1 

    Range
    101..208
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    34926775..34926882
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    34955301..34955408
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases