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RPS17P14 ribosomal protein S17 pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 100271074, updated on 10-Oct-2023

Summary

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Official Symbol
RPS17P14provided by HGNC
Official Full Name
ribosomal protein S17 pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:35534
See related
AllianceGenome:HGNC:35534
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
RPS17_6_941
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Genomic context

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Location:
8q23.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (108379159..108379545, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (109507605..109507991, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (109391388..109391774, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene aurora kinase B pseudogene 1 Neighboring gene MPRA-validated peak7146 silencer Neighboring gene eukaryotic translation initiation factor 3 subunit E Neighboring gene uncharacterized LOC105375704 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:109298807-109299390 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:109299391-109299976 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19467 Neighboring gene ER membrane protein complex subunit 2 Neighboring gene dnaJ homolog subfamily B member 6-like

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

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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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_011164.1 

    Range
    101..487
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    108379159..108379545 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    109507605..109507991 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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