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RPL6P17 ribosomal protein L6 pseudogene 17 [ Homo sapiens (human) ]

Gene ID: 100131229, updated on 13-May-2022

Summary

Official Symbol
RPL6P17provided by HGNC
Official Full Name
ribosomal protein L6 pseudogene 17provided by HGNC
Primary source
HGNC:HGNC:36914
See related
Ensembl:ENSG00000216754 AllianceGenome:HGNC:36914
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
RPL6_4_660
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Genomic context

See RPL6P17 in Genome Data Viewer
Location:
6p23
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (15102946..15104211, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (14976068..14977337, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (15103177..15104442, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 9180 Neighboring gene uncharacterized LOC105374945 Neighboring gene RNA, 7SL, cytoplasmic 332, pseudogene Neighboring gene uncharacterized LOC105374946

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_010828.1 

    Range
    101..1366
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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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    15102946..15104211 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    14976068..14977337 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)