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RNU6-544P RNA, U6 small nuclear 544, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481353, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-544Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 544, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47507
See related
Ensembl:ENSG00000200146 AllianceGenome:HGNC:47507
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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Location:
11q14.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (80527960..80528066)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (80462808..80462914)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (80239004..80239110)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369406 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:79868366-79868931 Neighboring gene uncharacterized LOC105369408 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5329 Neighboring gene NANOG hESC enhancer GRCh37_chr11:80274541-80275058 Neighboring gene ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 3 Neighboring gene uncharacterized LOC105369409

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_044495.1 

    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    80527960..80528066
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    80462808..80462914
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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