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RNA5SP99 RNA, 5S ribosomal pseudogene 99 [ Homo sapiens (human) ]

Gene ID: 106478993, updated on 10-Oct-2023

Summary

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Official Symbol
RNA5SP99provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 99provided by HGNC
Primary source
HGNC:HGNC:42897
See related
AllianceGenome:HGNC:42897
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
RN5S99
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Genomic context

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See RNA5SP99 in Genome Data Viewer
Location:
2p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (81496238..81496327, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (81496789..81496878, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (81723362..81723451, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene CHMP4A pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 1815 Neighboring gene uncharacterized LOC102724542 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:81884908-81886107 Neighboring gene uncharacterized LOC105374828 Neighboring gene uncharacterized LOC105374829

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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Other Names

  • RNA, 5S ribosomal 99

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_044042.1 

    Range
    101..190
    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    81496238..81496327 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    81496789..81496878 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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