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RPL21P10 ribosomal protein L21 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 319143, updated on 23-Nov-2021

Summary

Official Symbol
RPL21P10provided by HGNC
Official Full Name
ribosomal protein L21 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:19795
See related
Ensembl:ENSG00000239272
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
RPL21_49_1395
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Genomic context

See RPL21P10 in Genome Data Viewer
Location:
14q24.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (77683190..77684027, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (78149533..78150370, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene serine palmitoyltransferase long chain base subunit 2 Neighboring gene RNA, 7SL, cytoplasmic 587, pseudogene Neighboring gene cytochrome c oxidase subunit 6C pseudogene 11 Neighboring gene alkB homolog 1, histone H2A dioxygenase Neighboring gene zinc finger MYND-type containing 19 pseudogene 1 Neighboring gene SRA stem-loop interacting RNA binding protein

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_002519.5 

    Range
    101..938
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    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_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    77683190..77684027 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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