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RPS29P2 ribosomal protein S29 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 619452, updated on 10-Oct-2023

Summary

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Official Symbol
RPS29P2provided by HGNC
Official Full Name
ribosomal protein S29 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:31083
See related
AllianceGenome:HGNC:31083
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
HsT23291; RPS29_12_897
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Genomic context

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Location:
8p11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (41271404..41271659)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (41545031..41545286)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (41128923..41129178)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379771 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41052497-41053016 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41053017-41053536 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27281 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:41133705-41134289 Neighboring gene microRNA 548ao Neighboring gene secreted frizzled related protein 1 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr8:41165170-41165941 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41165942-41166712 Neighboring gene RNA, U6 small nuclear 895, pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr8:41168632-41169159 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:41179229-41179970 Neighboring gene small nucleolar RNA, C/D box 65B

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_009781.2 

    Range
    101..356
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    41271404..41271659
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    41545031..41545286
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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