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RNU5A-4P RNA, U5A small nuclear 4, pseudogene [ Homo sapiens (human) ]

Gene ID: 100873870, updated on 17-Sep-2024

Summary

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Official Symbol
RNU5A-4Pprovided by HGNC
Official Full Name
RNA, U5A small nuclear 4, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42521
See related
Ensembl:ENSG00000252397 AllianceGenome:HGNC:42521
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 RNU5A-4P in Genome Data Viewer
Location:
13q13.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (33829539..33829649, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (33047019..33047129, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (34403676..34403786, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene StAR related lipid transfer domain containing 13 Neighboring gene uncharacterized LOC102723406 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7582 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7583 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7584 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7585 Neighboring gene uncharacterized LOC107984551 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5256 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5257 Neighboring gene replication factor C subunit 3 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:34514923-34515422 Neighboring gene uncharacterized LOC105370156 Neighboring gene uncharacterized LOC107984589

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)

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_032643.1 

    Range
    101..211
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    33829539..33829649 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    33047019..33047129 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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