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RPS7P6 ribosomal protein S7 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 100270869, updated on 10-Dec-2024

Summary

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Official Symbol
RPS7P6provided by HGNC
Official Full Name
ribosomal protein S7 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:36334
See related
Ensembl:ENSG00000215278 AllianceGenome:HGNC:36334
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
RPS7_3_462
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Genomic context

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See RPS7P6 in Genome Data Viewer
Location:
4p15.32
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (17427667..17428349, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (17409463..17410145, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (17429290..17429972, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986219 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:17286136-17286636 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:17286637-17287137 Neighboring gene small nucleolar RNA, H/ACA box 75B Neighboring gene ReSE screen-validated silencer GRCh37_chr4:17437892-17438170 Neighboring gene uncharacterized LOC124900676 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:17472355-17472854 Neighboring gene Sharpr-MPRA regulatory region 11631 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15310 Neighboring gene quinoid dihydropteridine reductase

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_010094.2 

    Range
    101..783
    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
    17427667..17428349 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    17409463..17410145 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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