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RPL6P22 ribosomal protein L6 pseudogene 22 [ Homo sapiens (human) ]

Gene ID: 388460, updated on 10-Oct-2023

Summary

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Official Symbol
RPL6P22provided by HGNC
Official Full Name
ribosomal protein L6 pseudogene 22provided by HGNC
Primary source
HGNC:HGNC:36220
See related
Ensembl:ENSG00000240738 AllianceGenome:HGNC:36220
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
RPL6_7_890
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Genomic context

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Location:
8p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (33859348..33860248, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (34130630..34131530, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (33716866..33717766, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene RNA, 7SL, cytoplasmic 457, pseudogene Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:33612557-33613756 Neighboring gene uncharacterized LOC105379364 Neighboring gene VENT homeobox pseudogene 5 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:33715229-33715729 Neighboring gene NANOG hESC enhancer GRCh37_chr8:33773772-33774273 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_103242 Neighboring gene CYCS pseudogene 3 Neighboring gene MPRA-validated peak6990 silencer Neighboring gene VISTA enhancer hs1715 Neighboring gene uncharacterized LOC105379366 Neighboring gene uncharacterized LOC105379364

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_010561.1 

    Range
    101..1001
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    33859348..33860248 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    34130630..34131530 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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