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RNU6-1059P RNA, U6 small nuclear 1059, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480031, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-1059Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1059, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48022
See related
Ensembl:ENSG00000200622 AllianceGenome:HGNC:48022
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 RNU6-1059P in Genome Data Viewer
Location:
4q22.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (95868667..95868764, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (99183846..99183943, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (96789818..96789915, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein L30 pseudogene 6 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:96650673-96651268 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:96719717-96720414 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:96759303-96759905 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96760761-96761262 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96761263-96761762 Neighboring gene NANOG hESC enhancer GRCh37_chr4:96791095-96791601 Neighboring gene pyruvate dehydrogenase E1 subunit alpha 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96862743-96863244 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:96863245-96863744 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:97023059-97024258 Neighboring gene RNA, U6 small nuclear 34, pseudogene Neighboring gene talin 2 pseudogene

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_044156.1 

    Range
    101..198
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    95868667..95868764 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    99183846..99183943 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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