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RNU6-356P RNA, U6 small nuclear 356, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479724, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-356Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 356, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47319
See related
Ensembl:ENSG00000206867 AllianceGenome:HGNC:47319
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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Location:
8p11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (41032892..41032998)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (41306427..41306533)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (40890411..40890517)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379389 Neighboring gene uncharacterized LOC105379390 Neighboring gene MPRA-validated peak7001 silencer Neighboring gene NANOG hESC enhancer GRCh37_chr8:40915338-40915839 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:40930517-40931040 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:40932557-40933440 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:41008706-41009905 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:41013787-41014986 Neighboring gene uncharacterized LOC105379771 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41052497-41053016 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41053017-41053536 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27281 Neighboring gene microRNA 548ao Neighboring gene secreted frizzled related protein 1

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_043775.1 

    Range
    101..207
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    41032892..41032998
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    41306427..41306533
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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