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RPL31P63 ribosomal protein L31 pseudogene 63 [ Homo sapiens (human) ]

Gene ID: 100271392, updated on 10-Oct-2023

Summary

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Official Symbol
RPL31P63provided by HGNC
Official Full Name
ribosomal protein L31 pseudogene 63provided by HGNC
Primary source
HGNC:HGNC:35666
See related
Ensembl:ENSG00000236735 AllianceGenome:HGNC:35666
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
RPL31_36_1782
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Genomic context

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See RPL31P63 in Genome Data Viewer
Location:
Xq13.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (68600072..68600517)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (67033597..67034042)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (67819914..67820359)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:67718059-67718733 Neighboring gene Yip1 domain family member 6 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:67767078-67767642 Neighboring gene RNA, U6 small nuclear 245, pseudogene Neighboring gene Sharpr-MPRA regulatory region 12156 Neighboring gene cytochrome c oxidase subunit 6C pseudogene 12 Neighboring gene StAR related lipid transfer domain containing 8 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:67899756-67899932 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:67900175-67900675 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20886

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_010170.1 

    Range
    101..546
    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
    68600072..68600517
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    67033597..67034042
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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