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RNU6-505P RNA, U6 small nuclear 505, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479790, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-505Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 505, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47468
See related
Ensembl:ENSG00000207156 AllianceGenome:HGNC:47468
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RNU6-505P in Genome Data Viewer
Location:
3q24
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (146996607..146996713, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (149751904..149752010, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (146714394..146714500, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene PLSCR5 antisense RNA 1 Neighboring gene phospholipid scramblase family member 5 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:146498699-146499694 Neighboring gene long intergenic non-protein coding RNA 2010 Neighboring gene uncharacterized LOC112268449 Neighboring gene ribosomal protein L21 pseudogene 71

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_044272.1 

    Range
    101..207
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    146996607..146996713 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    149751904..149752010 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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