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RPS12P27 ribosomal protein S12 pseudogene 27 [ Homo sapiens (human) ]

Gene ID: 100271552, updated on 29-Mar-2018

Summary

Official Symbol
RPS12P27provided by HGNC
Official Full Name
ribosomal protein S12 pseudogene 27provided by HGNC
Primary source
HGNC:HGNC:35892
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
RPS12_13_1490

Genomic context

See RPS12P27 in Genome Data Viewer
Location:
16q22.1
Annotation release Status Assembly Chr Location
109 current GRCh38.p12 (GCF_000001405.38) 16 NC_000016.10 (68209381..68209824)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (68243284..68243727)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 359, pseudogene Neighboring gene DEAD-box helicase 28 Neighboring gene dihydrouridine synthase 2 Neighboring gene nuclear factor of activated T cells 3 Neighboring gene epithelial splicing regulatory protein 2 Neighboring gene microRNA 6773 Neighboring gene phospholipase A2 group XV

Genomic regions, transcripts, and products

Bibliography

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

NCBI Reference Sequences (RefSeq)

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_010994.1 

    Range
    101..544
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p12 Primary Assembly

    Range
    68209381..68209824
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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