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RPS2P7 ribosomal protein S2 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 86781, updated on 23-Nov-2021

Summary

Official Symbol
RPS2P7provided by HGNC
Official Full Name
ribosomal protein S2 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:15838
See related
Ensembl:ENSG00000235508
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
RPS2L1; dJ688G8.1; RPS2_27_1706
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Genomic context

See RPS2P7 in Genome Data Viewer
Location:
20q13.12
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (45640452..45641393, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (44269091..44270032, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene WAP four-disulfide core domain 8 Neighboring gene cyclin B1 interacting protein 1 pseudogene 2 Neighboring gene WAP four-disulfide core domain 9 Neighboring gene WAP four-disulfide core domain 10A Neighboring gene WAP four-disulfide core domain 11 Neighboring gene WAP four-disulfide core domain 10B Neighboring gene WAP four-disulfide core domain 13 Neighboring gene microRNA 3617

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_000946.5 

    Range
    101..1042
    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_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    45640452..45641393 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_080566.1: Suppressed sequence

    Description
    NM_080566.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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