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RPL10P13 ribosomal protein L10 pseudogene 13 [ Homo sapiens (human) ]

Gene ID: 390345, updated on 13-May-2022

Summary

Official Symbol
RPL10P13provided by HGNC
Official Full Name
ribosomal protein L10 pseudogene 13provided by HGNC
Primary source
HGNC:HGNC:52346
See related
Ensembl:ENSG00000258245 AllianceGenome:HGNC:52346
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See RPL10P13 in Genome Data Viewer
Location:
12q21.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (75688725..75689096, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (75663727..75664098, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (76082505..76082876, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369844 Neighboring gene phosphogluconate dehydrogenase pseudogene 2 Neighboring gene uncharacterized LOC107984533 Neighboring gene small nucleolar RNA SNORA70 Neighboring gene uncharacterized LOC105369846

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_009872.3 

    Range
    101..472
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    75688725..75689096 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    75663727..75664098 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)