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RNVU1-19 RNA, variant U1 small nuclear 19 [ Homo sapiens (human) ]

Gene ID: 101954277, updated on 18-Aug-2020

Summary

Official Symbol
RNVU1-19provided by HGNC
Official Full Name
RNA, variant U1 small nuclear 19provided by HGNC
Primary source
HGNC:HGNC:48324
See related
Ensembl:ENSG00000275538
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
vU1.13; vU1.19; RNU1-126; RNU1-147; RNVU1-13

Genomic context

See RNVU1-19 in Genome Data Viewer
Location:
1p11.2
Exon count:
1
Annotation release Status Assembly Chr Location
109.20200815 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (120850819..120850985, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene NBPF member 26 Neighboring gene tRNA-Asn (anticodon GTT) 7-1 Neighboring gene peptidylprolyl isomerase A like 4A Neighboring gene uncharacterized LOC100996720 Neighboring gene long intergenic non-protein coding RNA 623

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

General gene information

Other Names

  • RNA, variant U1 small nuclear 13

Gene Ontology Provided by GOA

Function Evidence Code Pubs
pre-mRNA 5'-splice site binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
mRNA 5'-splice site recognition IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
U1 snRNP IEA
Inferred from Electronic Annotation
more info
 

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_104086.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC253572
    Related
    ENST00000613023.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20200815

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
    120850819..120850985 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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