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RNU6-1286P RNA, U6 small nuclear 1286, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481586, updated on 4-Mar-2025

Summary

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Official Symbol
RNU6-1286Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1286, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48249
See related
Ensembl:ENSG00000206598 AllianceGenome:HGNC:48249
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 RNU6-1286P in Genome Data Viewer
Location:
6q22.31
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (121354354..121354460)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (122541443..122541549)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (121675500..121675606)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377977 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_88787 Neighboring gene TBC1 domain family member 32 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_88931 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89007 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89060 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89073 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89101 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_89176 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17513 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 25019 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr6:121697099-121697600 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr6:121697601-121698100 Neighboring gene ribosomal protein S15a pseudogene 21 Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 29

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_044311.1 

    Range
    101..207
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    121354354..121354460
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    122541443..122541549
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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