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RNVU1-2A RNA, variant U1 small nuclear 2A [ Homo sapiens (human) ]

Gene ID: 6063, updated on 12-Oct-2019

Summary

Official Symbol
RNVU1-2Aprovided by HGNC
Official Full Name
RNA, variant U1 small nuclear 2Aprovided by HGNC
Primary source
HGNC:HGNC:54430
See related
Ensembl:ENSG00000278099
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
U1P2A; RNU1P2; vU1.2a; RNU1-12P; RNVU1.2a

Genomic context

See RNVU1-2A 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 (144551779..144551943, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene NBPF member 15 Neighboring gene profilin 1 pseudogene 6 Neighboring gene uncharacterized LOC105371211 Neighboring gene uncharacterized LOC105379574 Neighboring gene uncharacterized LOC107985110 Neighboring gene tRNA-Asn (GTT) 3-2

Genomic regions, transcripts, and products

General gene information

Other Names

  • RNA, U1 small nuclear 12 (pseudogene)
  • RNA, U1 small nuclear pseudogene 2
  • RNA, variant U1 small nuclear 11

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_145576.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC253578
    Related
    ENST00000617626.1

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
    144551779..144551943 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NT_187520.1 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    63074..63238 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_001184.2: Suppressed sequence

    Description
    NG_001184.2: This RefSeq was removed because it is now thought that this gene is transcribed.
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