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RPL36P18 ribosomal protein L36 pseudogene 18 [ Homo sapiens (human) ]

Gene ID: 100271394, updated on 10-Oct-2023

Summary

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Official Symbol
RPL36P18provided by HGNC
Official Full Name
ribosomal protein L36 pseudogene 18provided by HGNC
Primary source
HGNC:HGNC:36856
See related
AllianceGenome:HGNC:36856
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
RPL36_10_1804
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Genomic context

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Location:
Xq23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (115198399..115198796)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (113607016..113607413)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (114432962..114433359)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene leucine rich repeats and calponin homology domain containing 2 Neighboring gene TMSB4X pseudogene 7 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:114424095-114424596 Neighboring gene RBMX like 3 Neighboring gene leucine zipper protein 4 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:114552544-114553121 Neighboring gene uncharacterized LOC107985681 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:114579651-114580150 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:114606578-114607435 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:114607575-114608077

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_010182.3 

    Range
    101..498
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    115198399..115198796
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    113607016..113607413
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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