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RPL26P32 ribosomal protein L26 pseudogene 32 [ Homo sapiens (human) ]

Gene ID: 400055, updated on 17-Sep-2024

Summary

Official Symbol
RPL26P32provided by HGNC
Official Full Name
ribosomal protein L26 pseudogene 32provided by HGNC
Primary source
HGNC:HGNC:36448
See related
Ensembl:ENSG00000230291 AllianceGenome:HGNC:36448
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_12_1262
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Genomic context

See RPL26P32 in Genome Data Viewer
Location:
12q21.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (80102859..80103357, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (80081622..80082120, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (80496639..80497137, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein L7 pseudogene 38 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80477061-80477602 Neighboring gene RNA, U7 small nuclear 106 pseudogene Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80543056-80543602 Neighboring gene otogelin like Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4684 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80643124-80643716 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:80643717-80644308 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:80713982-80714515 Neighboring gene RN7SK pseudogene 261 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:80864089-80864632 Neighboring gene uncharacterized LOC124902975 Neighboring gene protein tyrosine phosphatase receptor type Q

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Genome-wide association with bone mass and geometry in the Framingham Heart Study.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_006965.2 

    Range
    101..599
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    80102859..80103357 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    80081622..80082120 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)