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RPL7AP27 ribosomal protein L7a pseudogene 27 [ Homo sapiens (human) ]

Gene ID: 152663, updated on 17-Sep-2024

Summary

Official Symbol
RPL7AP27provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 27provided by HGNC
Primary source
HGNC:HGNC:36806
See related
Ensembl:ENSG00000242169 AllianceGenome:HGNC:36806
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_11_540
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Genomic context

See RPL7AP27 in Genome Data Viewer
Location:
4q35.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (188349318..188350047, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (191696523..191697252, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (189270472..189271201, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:189080404-189081603 Neighboring gene long intergenic non-protein coding RNA 2434 Neighboring gene uncharacterized LOC105377607 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_76925 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:189117054-189117752 Neighboring gene uncharacterized LOC105377608 Neighboring gene interactor of little elongation complex ELL subunit 2 pseudogene 1

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_010457.1 

    Range
    101..830
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    188349318..188350047 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187545.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    7896..8625 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    191696523..191697252 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)