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RPL7P59 ribosomal protein L7 pseudogene 59 [ Homo sapiens (human) ]

Gene ID: 643308, updated on 10-Oct-2023

Summary

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Official Symbol
RPL7P59provided by HGNC
Official Full Name
ribosomal protein L7 pseudogene 59provided by HGNC
Primary source
HGNC:HGNC:49215
See related
AllianceGenome:HGNC:49215
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
7q35
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (145040351..145040962, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (146220672..146221283, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (144737444..144738055, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene karyopherin subunit alpha 2 pseudogene Neighboring gene EI24 pseudogene 4 Neighboring gene NANOG hESC enhancer GRCh37_chr7:144782351-144782852 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:144880176-144881375 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:144921770-144922322 Neighboring gene MPRA-validated peak6814 silencer Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr7:145115119-145116318 Neighboring gene MPRA-validated peak6815 silencer Neighboring gene MPRA-validated peak6816 silencer Neighboring gene DPY19L4 pseudogene 2 Neighboring gene MPRA-validated peak6818 silencer Neighboring gene uncharacterized LOC105375553

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. Toward a complete human genome sequence. Sanger Center, et al. Genome Res, 1998 Nov. PMID 9847074

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_011222.2 

    Range
    101..712
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    145040351..145040962 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    146220672..146221283 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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