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RPL26P27 ribosomal protein L26 pseudogene 27 [ Homo sapiens (human) ]

Gene ID: 100271471, updated on 13-May-2022

Summary

Official Symbol
RPL26P27provided by HGNC
Official Full Name
ribosomal protein L26 pseudogene 27provided by HGNC
Primary source
HGNC:HGNC:36735
See related
Ensembl:ENSG00000226493 AllianceGenome:HGNC:36735
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
RPL26_15_1055
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Genomic context

See RPL26P27 in Genome Data Viewer
Location:
10q21.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (68499490..68500009)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (69368728..69369247)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (70259247..70259766)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene DNA replication helicase/nuclease 2 Neighboring gene ribosomal protein L26 pseudogene 29 Neighboring gene RNA, 5S ribosomal pseudogene 319 Neighboring gene solute carrier family 25 member 16 Neighboring gene Sharpr-MPRA regulatory region 5966 Neighboring gene transmembrane protein 14D, pseudogene

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_010572.2 

    Range
    101..620
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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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    68499490..68500009
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    69368728..69369247
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)