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RPL7AP52 ribosomal protein L7a pseudogene 52 [ Homo sapiens (human) ]

Gene ID: 100271534, updated on 10-Oct-2023

Summary

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Official Symbol
RPL7AP52provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 52provided by HGNC
Primary source
HGNC:HGNC:36233
See related
Ensembl:ENSG00000225354 AllianceGenome:HGNC:36233
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
RPL7A_18_1082
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Genomic context

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See RPL7AP52 in Genome Data Viewer
Location:
10q23.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (94882564..94883349)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (95761708..95762493)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (96642321..96643106)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene MT-ND4 pseudogene 19 Neighboring gene cytochrome P450 family 2 subfamily C member 19 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:96590143-96590741 Neighboring gene cytochrome P450 family 2 subfamily C member 58, pseudogene Neighboring gene cytochrome P450 family 2 subfamily C member 115, pseudogene Neighboring gene CYP2C9 promoter Neighboring gene MT-ND4 pseudogene 20 Neighboring gene cytochrome P450 family 2 subfamily C member 9

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_010903.1 

    Range
    101..886
    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    94882564..94883349
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    95761708..95762493
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Other Literature Sources
Molecular Biology Databases