U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

RNU6-557P RNA, U6 small nuclear 557, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479814, updated on 10-Oct-2023

Summary

Go to the top of the page Help
Official Symbol
RNU6-557Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 557, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47520
See related
Ensembl:ENSG00000252651 AllianceGenome:HGNC:47520
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See RNU6-557P in Genome Data Viewer
Location:
3p13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (73092148..73092257, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (73133653..73133762, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (73141299..73141408, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene protein phosphatase 4 regulatory subunit 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20098 Neighboring gene small nucleolar RNA U13 Neighboring gene endogenous Bornavirus like nucleoprotein 2 Neighboring gene uncharacterized LOC107986098 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:73159463-73160025 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:73160026-73160587 Neighboring gene RNA, U2 small nuclear 64, pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:73213631-73214237 Neighboring gene GPATCH11 pseudogene 1

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

Go to the top of the page Help

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_044470.1 

    Range
    101..210
    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
    73092148..73092257 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    73133653..73133762 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases