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RPL21P69 ribosomal protein L21 pseudogene 69 [ Homo sapiens (human) ]

Gene ID: 642738, updated on 10-Dec-2024

Summary

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Official Symbol
RPL21P69provided by HGNC
Official Full Name
ribosomal protein L21 pseudogene 69provided by HGNC
Primary source
HGNC:HGNC:36753
See related
Ensembl:ENSG00000216480 AllianceGenome:HGNC:36753
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_27_774
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Genomic context

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See RPL21P69 in Genome Data Viewer
Location:
6q25.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (159526014..159526567, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (160771651..160772204, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (159947046..159947599, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2529 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:159843463-159844278 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:159883544-159884049 Neighboring gene uncharacterized LOC101929142 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:159914293-159914495 Neighboring gene uncharacterized LOC105378085 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:160015262-160016461 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:160023547-160024063 Neighboring gene uncharacterized LOC124901450

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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_009725.2 

    Range
    101..654
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    159526014..159526567 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    160771651..160772204 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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