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RNU1-76P RNA, U1 small nuclear 76, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481617, updated on 10-Oct-2023

Summary

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Official Symbol
RNU1-76Pprovided by HGNC
Official Full Name
RNA, U1 small nuclear 76, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48418
See related
Ensembl:ENSG00000199773 AllianceGenome:HGNC:48418
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:
5p15.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (7980146..7980304)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (7920303..7920461)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (7980259..7980417)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900936 Neighboring gene semaphorin 5A pseudogene Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr5:7928453-7929652 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr5:7995658-7996857 Neighboring gene uncharacterized LOC124900937 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:8060973-8061591 Neighboring gene uncharacterized LOC102723339

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_044560.1 

    Range
    101..259
    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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    7980146..7980304
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    7920303..7920461
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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