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RNVU1-34 RNA, variant U1 small nuclear 34 [ Homo sapiens (human) ]

Gene ID: 106480177, updated on 23-Nov-2021

Summary

Official Symbol
RNVU1-34provided by HGNC
Official Full Name
RNA, variant U1 small nuclear 34provided by HGNC
Primary source
HGNC:HGNC:48427
See related
Ensembl:ENSG00000200997
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
U1A7; RNU1-85P
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Genomic context

See RNVU1-34 in Genome Data Viewer
Location:
17q22
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (58679527..58679690, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (56756888..56757051, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene testis expressed 14, intercellular bridge forming factor Neighboring gene RNA, U1 small nuclear 108, pseudogene Neighboring gene immunoglobulin (CD79A) binding protein 1 pseudogene 2 Neighboring gene RNA, U1 small nuclear 52, pseudogene Neighboring gene uncharacterized LOC105371843 Neighboring gene RAD51 paralog C Neighboring gene protein phosphatase, Mg2+/Mn2+ dependent 1E Neighboring gene RNA, U6 small nuclear 518, pseudogene

Genomic regions, transcripts, and products

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_045398.1 

    Range
    101..264
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    58679527..58679690 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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