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RPL27P12 ribosomal protein L27 pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 100271302, updated on 23-Nov-2021

Summary

Official Symbol
RPL27P12provided by HGNC
Official Full Name
ribosomal protein L27 pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:36736
See related
Ensembl:ENSG00000239215
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
RPL27_4_1293
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Genomic context

See RPL27P12 in Genome Data Viewer
Location:
12q24.31
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (123721218..123721642, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (124205765..124206189, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene general transcription factor IIH subunit 3 Neighboring gene tectonic family member 2 Neighboring gene uncharacterized LOC105370042 Neighboring gene ATPase H+ transporting V0 subunit a2 Neighboring gene uncharacterized LOC105370044 Neighboring gene dynein axonemal heavy chain 10 Neighboring gene Sharpr-MPRA regulatory region 5794

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_011023.1 

    Range
    101..525
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    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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    123721218..123721642 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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