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RPS17P5 ribosomal protein S17 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 442216, updated on 13-May-2022

Summary

Official Symbol
RPS17P5provided by HGNC
Official Full Name
ribosomal protein S17 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:21352
See related
Ensembl:ENSG00000060303 AllianceGenome:HGNC:21352
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
RPS17L4; dJ753D5.2; RPS17_4_700
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Genomic context

See RPS17P5 in Genome Data Viewer
Location:
6p12.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (50857209..50857687, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (50699961..50700439, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (50824922..50825400, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375084 Neighboring gene uncharacterized LOC124901490 Neighboring gene transcription factor AP-2 beta Neighboring gene transportin 3 pseudogene Neighboring gene ferritin heavy chain 1 pseudogene 5

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_005089.5 

    Range
    101..579
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    GenBank, FASTA, Sequence Viewer (Graphics)

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
    50857209..50857687 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    50699961..50700439 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001013733.1: Suppressed sequence

    Description
    NM_001013733.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.