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RNA5SP166 RNA, 5S ribosomal pseudogene 166 [ Homo sapiens (human) ]

Gene ID: 100873431, updated on 10-Oct-2023

Summary

Official Symbol
RNA5SP166provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 166provided by HGNC
Primary source
HGNC:HGNC:43066
See related
Ensembl:ENSG00000201846 AllianceGenome:HGNC:43066
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
RN5S166
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Genomic context

Location:
4q31.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (148557947..148558048)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (151882008..151882109)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (149479099..149479200)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900798 Neighboring gene uncharacterized LOC107986195 Neighboring gene argininosuccinate synthetase 1 pseudogene 8 Neighboring gene uncharacterized LOC105377483 Neighboring gene uncharacterized LOC124900797

Genomic regions, transcripts, and products

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_033645.1 

    Range
    101..202
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    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    148557947..148558048
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    151882008..151882109
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)