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RPS18P12 ribosomal protein S18 pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 388339, updated on 25-Jan-2022

Summary

Official Symbol
RPS18P12provided by HGNC
Official Full Name
ribosomal protein S18 pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:35967
See related
Ensembl:ENSG00000230897 AllianceGenome:HGNC:35967
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_4_1516
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Genomic context

See RPS18P12 in Genome Data Viewer
Location:
17p12
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (14705037..14705576, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (14608354..14608893, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985080 Neighboring gene uncharacterized LOC107984996 Neighboring gene uncharacterized LOC105371545 Neighboring gene long intergenic non-protein coding RNA 2096

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_011261.2 

    Range
    101..640
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    14705037..14705576 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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