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MRPS17P3 mitochondrial ribosomal protein S17 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 359757, updated on 10-Oct-2023

Summary

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Official Symbol
MRPS17P3provided by HGNC
Official Full Name
mitochondrial ribosomal protein S17 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:29736
See related
Ensembl:ENSG00000239226 AllianceGenome:HGNC:29736
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:
3p12.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (78525082..78525507)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (78579838..78580263)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (78574232..78574657)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene RNA, 7SL, cytoplasmic 647, pseudogene Neighboring gene RN7SK pseudogene 61 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:78315096-78316295 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:78371863-78372653 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr3:78392873-78394072 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:78402403-78402950 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:78630276-78631137 Neighboring gene roundabout guidance receptor 1 Neighboring gene Sharpr-MPRA regulatory region 7147 Neighboring gene ribosomal protein S12 pseudogene 6 Neighboring gene Sharpr-MPRA regulatory region 6803 Neighboring gene RNA, 7SL, cytoplasmic 751, pseudogene

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. Identification and characterization of over 100 mitochondrial ribosomal protein pseudogenes in the human genome. Zhang Z, et al. Genomics, 2003 May. PMID 12706105

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_002873.3 

    Range
    101..526
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    78525082..78525507
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    78579838..78580263
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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