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RNVU1-6 RNA, variant U1 small nuclear 6 [ Homo sapiens (human) ]

Gene ID: 101954276, updated on 12-Oct-2019

Summary

Official Symbol
RNVU1-6provided by HGNC
Official Full Name
RNA, variant U1 small nuclear 6provided by HGNC
Primary source
HGNC:HGNC:48314
See related
Ensembl:ENSG00000201558
Gene type
snRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
vU1.6; RNU1-99

Genomic context

See RNVU1-6 in Genome Data Viewer
Location:
1q21.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (146052081..146052244, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene tRNA-Lys (anticodon CTT) 2-1 Neighboring gene uncharacterized LOC107985594 Neighboring gene long intergenic non-protein coding RNA 1719 Neighboring gene NBPF member 10

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000001.11 Chromosome 1 Reference GRCh38.p13 Primary Assembly

Interactions

Products Interactant Other Gene Complex Source Pubs Description

NCBI Reference Sequences (RefSeq)

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.

RNA

  1. NR_104085.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC239799
    Related
    ENST00000364688.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    146052081..146052244 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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