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RPL7AP26 ribosomal protein L7a pseudogene 26 [ Homo sapiens (human) ]

Gene ID: 728128, updated on 13-May-2022

Summary

Official Symbol
RPL7AP26provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 26provided by HGNC
Primary source
HGNC:HGNC:36815
See related
Ensembl:ENSG00000214988 AllianceGenome:HGNC:36815
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
RPL7A_8_496
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Genomic context

See RPL7AP26 in Genome Data Viewer
Location:
4q21.22
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (82490762..82491655, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (85820046..85820939, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (83411915..83412808, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene enolase-phosphatase 1 Neighboring gene uncharacterized LOC105377310 Neighboring gene transmembrane protein 150C Neighboring gene ribosomal protein S6 pseudogene Neighboring gene Sharpr-MPRA regulatory region 10449

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_010339.2 

    Range
    101..994
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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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    82490762..82491655 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    85820046..85820939 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)