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RNU6-695P RNA, U6 small nuclear 695, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481400, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-695Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 695, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47658
See related
Ensembl:ENSG00000212459 AllianceGenome:HGNC:47658
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 RNU6-695P in Genome Data Viewer
Location:
1p22.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (90253456..90253559, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (90096849..90096952, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (90719014..90719117, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancers GRCh37_chr1:90460321-90460887 and GRCh37_chr1:90460888-90461453 Neighboring gene zinc finger protein 326 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:90528154-90528660 Neighboring gene uncharacterized LOC105378848 Neighboring gene NANOG hESC enhancer GRCh37_chr1:90597824-90598325 Neighboring gene NANOG hESC enhancer GRCh37_chr1:90642009-90642541 Neighboring gene uncharacterized LOC105378849 Neighboring gene NANOG hESC enhancer GRCh37_chr1:90739373-90739874 Neighboring gene NANOG hESC enhancer GRCh37_chr1:90741293-90741867 Neighboring gene uncharacterized LOC107985088 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1301 Neighboring gene uncharacterized LOC105378850

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_044880.1 

    Range
    101..204
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    90253456..90253559 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    90096849..90096952 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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