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RNU6-1027P RNA, U6 small nuclear 1027, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481505, updated on 10-Oct-2023

Summary

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Official Symbol
RNU6-1027Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1027, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47990
See related
Ensembl:ENSG00000206725 AllianceGenome:HGNC:47990
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 RNU6-1027P in Genome Data Viewer
Location:
2q36.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (229973315..229973421)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (230455997..230456103)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (230838031..230838137)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene F-box protein 36 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:230808542-230809042 Neighboring gene RNA, U6 small nuclear 964, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:230817679-230818543 Neighboring gene uncharacterized LOC105373924 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:230829825-230830039 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:230871505-230871694 Neighboring gene uncharacterized LOC107985996 Neighboring gene solute carrier family 16 member 14 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:230910722-230911921 Neighboring gene RNY4 pseudogene 19

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_045544.1 

    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    229973315..229973421
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    230455997..230456103
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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