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RNU6-632P RNA, U6 small nuclear 632, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479846, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-632Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 632, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47595
See related
Ensembl:ENSG00000251711 AllianceGenome:HGNC:47595
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 RNU6-632P in Genome Data Viewer
Location:
10p12.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (25819363..25819426, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (25844338..25844401, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (26108292..26108355, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 836 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:25983020-25983520 Neighboring gene histone cell cycle regulator pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chr10:26005209-26005710 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:26027519-26027690 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:26055160-26055775 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:26063372-26063916 Neighboring gene RNA, 5S ribosomal pseudogene 306 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2234 Neighboring gene uncharacterized LOC124902396 Neighboring gene uncharacterized LOC124902397 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3163 Neighboring gene uncharacterized LOC105376460

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_044728.1 

    Range
    101..164
    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
    25819363..25819426 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    25844338..25844401 complement
    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