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RNU6-75P RNA, U6 small nuclear 75, pseudogene [ Homo sapiens (human) ]

Gene ID: 100873776, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-75Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 75, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42565
See related
Ensembl:ENSG00000251753 AllianceGenome:HGNC:42565
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RNU6-75
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Genomic context

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Location:
13q31.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (90781766..90781869, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (89984345..89984448, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (91434020..91434123, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:91147255-91147754 Neighboring gene long intergenic non-protein coding RNA 1049 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:91316129-91316630 Neighboring gene uncharacterized LOC107984572 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr13:91496709-91497278 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:91500507-91501257 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:91501258-91502007 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:91505936-91506676 Neighboring gene uncharacterized LOC105370311 Neighboring gene long intergenic non-protein coding RNA 410 Neighboring gene BRK1 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)

See Variation Viewer (GRCh38)

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_043308.1 

    Range
    101..204
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    90781766..90781869 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    89984345..89984448 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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