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RNA5SP34 RNA, 5S ribosomal pseudogene 34 [ Homo sapiens (human) ]

Gene ID: 100873366, updated on 10-Oct-2023

Summary

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Official Symbol
RNA5SP34provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 34provided by HGNC
Primary source
HGNC:HGNC:42610
See related
Ensembl:ENSG00000252696 AllianceGenome:HGNC:42610
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
RN5S34
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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 (90135712..90135841, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (89340092..89340221, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (90787966..90788095, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene peroxisomal biogenesis factor 12 pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 559 Neighboring gene fatty acyl-CoA reductase 1 pseudogene 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:90852143-90852366 Neighboring gene keratin 18 pseudogene 27 Neighboring gene microRNA 622

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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Other Names

  • RNA, 5S ribosomal 34

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_033514.1 

    Range
    101..230
    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
    90135712..90135841 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    89340092..89340221 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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