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RPL17P33 ribosomal protein L17 pseudogene 33 [ Homo sapiens (human) ]

Gene ID: 646909, updated on 10-Oct-2023

Summary

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Official Symbol
RPL17P33provided by HGNC
Official Full Name
ribosomal protein L17 pseudogene 33provided by HGNC
Primary source
HGNC:HGNC:36654
See related
Ensembl:ENSG00000243844 AllianceGenome:HGNC:36654
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
RPL17_19_888
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Genomic context

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Location:
8p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (29632070..29632683)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (29910424..29911037)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (29489586..29490199)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901925 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:29449049-29450248 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19073 Neighboring gene uncharacterized LOC105379352 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27203 Neighboring gene uncharacterized LOC124901926 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:29525986-29527185 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27204 Neighboring gene long intergenic non-protein coding RNA 589 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:29594328-29595186

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_011315.3 

    Range
    101..714
    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
    29632070..29632683
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    29910424..29911037
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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