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RNU6-284P RNA, U6 small nuclear 284, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481268, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-284Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 284, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47247
See related
Ensembl:ENSG00000223037 AllianceGenome:HGNC:47247
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 RNU6-284P in Genome Data Viewer
Location:
4q32.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (164620732..164620837)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (167968418..167968523)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (165541884..165541989)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene membrane associated ring-CH-type finger 1 Neighboring gene heat shock protein family A (Hsp70) member 5 pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162454-165162964 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162965-165163475 Neighboring gene acidic nuclear phosphoprotein 32 family member C, pseudogene Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165272175-165272792 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:165304399-165304900 Neighboring gene MPRA-validated peak5144 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:165597429-165597929 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_75752 Neighboring gene MPRA-validated peak5145 silencer Neighboring gene CHORDC1 pseudogene 3 Neighboring gene RNA, U6 small nuclear 668, pseudogene Neighboring gene small integral membrane protein 31

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_043845.1 

    Range
    101..206
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    164620732..164620837
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    167968418..167968523
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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