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RNU6-184P RNA, U6 small nuclear 184, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479648, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-184Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 184, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47147
See related
Ensembl:ENSG00000252323 AllianceGenome:HGNC:47147
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 RNU6-184P in Genome Data Viewer
Location:
Yq11.221
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (16336283..16336389, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (17242831..17242937, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (18448163..18448269, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA SNORA20 Neighboring gene RNA, U6 small nuclear 109, pseudogene Neighboring gene MED14-independent group 3 enhancer GRCh37_chrY:19155795-19156994 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrY:19177943-19178550 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrY:19178551-19179158 Neighboring gene surfeit 6 pseudogene 1 Neighboring gene elongin C pseudogene 35

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_043167.1 

    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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    16336283..16336389 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    17242831..17242937 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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