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RPS16P5 ribosomal protein S16 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 647190, updated on 13-May-2022

Summary

Official Symbol
RPS16P5provided by HGNC
Official Full Name
ribosomal protein S16 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:36183
See related
AllianceGenome:HGNC:36183
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPS16_3_702
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Genomic context

See RPS16P5 in Genome Data Viewer
Location:
6p12.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (53334460..53337617, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (53174193..53177350, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (53199258..53202415, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene ELOVL fatty acid elongase 5 Neighboring gene microRNA 5685 Neighboring gene Sharpr-MPRA regulatory region 4240 Neighboring gene ribosomal protein L31 pseudogene 28 Neighboring gene ribosomal protein L31 pseudogene 33

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.

RNA

  1. NR_046241.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL034374

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    53334460..53337617 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    53174193..53177350 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_010106.1: Suppressed sequence

    Description
    NG_010106.1: This RefSeq was permanently suppressed because there is evidence that this locus is transcribed.