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RPS18P3 ribosomal protein S18 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 100128258, updated on 17-Sep-2024

Summary

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Official Symbol
RPS18P3provided by HGNC
Official Full Name
ribosomal protein S18 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:36198
See related
Ensembl:ENSG00000242757 AllianceGenome:HGNC:36198
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
RPS18_2_171
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Genomic context

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See RPS18P3 in Genome Data Viewer
Location:
1q42.13
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (227430482..227431020)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (226619344..226619882)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (227618183..227618721)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904531 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:227543671-227544356 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:227544357-227545040 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:227576538-227577298 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:227583939-227585138 Neighboring gene long intergenic non-protein coding RNA 1641 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:227606019-227606211 Neighboring gene nuclear casein kinase and cyclin dependent kinase substrate 1 pseudogene 1 Neighboring gene basic transcription factor 3 pseudogene 9 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:227661907-227662406 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:227681476-227682162 Neighboring gene tubulin beta 8 class VIII pseudogene 10

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)

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_009969.2 

    Range
    101..639
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    227430482..227431020
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    226619344..226619882
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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