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RPS29P19 ribosomal protein S29 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 100271383, updated on 23-Nov-2021

Summary

Official Symbol
RPS29P19provided by HGNC
Official Full Name
ribosomal protein S29 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:36118
See related
Ensembl:ENSG00000243353
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
RPS29_4_1178
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Genomic context

See RPS29P19 in Genome Data Viewer
Location:
11q23.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (113751116..113751286, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (113621838..113622008, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene transmembrane serine protease 5 Neighboring gene mitochondrial translational release factor 1 like pseudogene 1 Neighboring gene zw10 kinetochore protein Neighboring gene cytochrome c oxidase subunit 7A2 like pseudogene Neighboring gene claudin 25

Genomic regions, transcripts, and products

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_010109.1 

    Range
    101..271
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    113751116..113751286 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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