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RPL39P18 ribosomal protein L39 pseudogene 18 [ Homo sapiens (human) ]

Gene ID: 100271025, updated on 13-May-2022

Summary

Official Symbol
RPL39P18provided by HGNC
Official Full Name
ribosomal protein L39 pseudogene 18provided by HGNC
Primary source
HGNC:HGNC:36111
See related
AllianceGenome:HGNC:36111
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
RPL39_7_347
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Genomic context

See RPL39P18 in Genome Data Viewer
Location:
3p24.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (20012403..20012801)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (20016471..20016869)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (20053895..20054293)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene protein phosphatase 2C like domain containing 1 Neighboring gene uncharacterized LOC124909352 Neighboring gene RNA, U4 small nuclear 85, pseudogene Neighboring gene SAP18 pseudogene 3 Neighboring gene CRISPRi-validated cis-regulatory element chr3.1018 Neighboring gene lysine acetyltransferase 2B Neighboring gene microRNA 3135a

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_010919.1 

    Range
    101..499
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    20012403..20012801
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    20016471..20016869
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)