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RNU4-76P RNA, U4 small nuclear 76, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480549, updated on 4-Mar-2025

Summary

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Official Symbol
RNU4-76Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 76, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47012
See related
Ensembl:ENSG00000201379 AllianceGenome:HGNC:47012
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 RNU4-76P in Genome Data Viewer
Location:
6q22.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (121542486..121542626, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (122729556..122729696, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (121863632..121863772, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene RNA, U4 small nuclear 35, pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89387 Neighboring gene transcription factor A, mitochondrial pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89523 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121892975-121893482 Neighboring gene RNA, U2 small nuclear 8, pseudogene Neighboring gene ReSE screen-validated silencer GRCh37_chr6:121925900-121926110 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:121940073-121940713 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:121941509-121942161 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:121948343-121949542 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89548 Neighboring gene solute carrier family 25 member 5 pseudogene 7

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_044201.1 

    Range
    101..241
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    121542486..121542626 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    122729556..122729696 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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