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RNU4-37P RNA, U4 small nuclear 37, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481183, updated on 10-Oct-2023

Summary

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Official Symbol
RNU4-37Pprovided by HGNC
Official Full Name
RNA, U4 small nuclear 37, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46973
See related
Ensembl:ENSG00000222146 AllianceGenome:HGNC:46973
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 RNU4-37P in Genome Data Viewer
Location:
8q23.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (112148742..112148825, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (113273766..113273849, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (113160971..113161054, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:112690362-112690868 Neighboring gene Sharpr-MPRA regulatory region 110 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:112735891-112736073 Neighboring gene uncharacterized LOC105375707 Neighboring gene H2A.Z histone pseudogene 7 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:112928926-112929652 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:113206999-113207584 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:113230017-113230753 Neighboring gene CUB and Sushi multiple domains 3 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:113479947-113480134 Neighboring gene small nucleolar RNA U13 Neighboring gene ribosomal protein L30 pseudogene 16

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_043162.1 

    Range
    101..184
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    112148742..112148825 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    113273766..113273849 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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