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SNORA2C small nucleolar RNA, H/ACA box 2C [ Homo sapiens (human) ]

Gene ID: 677815, updated on 13-May-2022

Summary

Official Symbol
SNORA2Cprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 2Cprovided by HGNC
Primary source
HGNC:HGNC:32624
See related
Ensembl:ENSG00000221491 MIM:615487; AllianceGenome:HGNC:32624
Gene type
snoRNA
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ACA34; MIR1291; SNORA34
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Genomic context

See SNORA2C in Genome Data Viewer
Location:
12q13.11
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (48654382..48654518, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (48616405..48616541, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (49048165..49048301, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 11 subfamily M member 1 pseudogene Neighboring gene uncharacterized LOC124902928 Neighboring gene KAT8 regulatory NSL complex subunit 2 Neighboring gene microRNA 1291 Neighboring gene small nucleolar RNA, H/ACA box 2A Neighboring gene small nucleolar RNA, H/ACA box 2B

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • ACA34 snoRNA
  • small nucleolar RNA, H/ACA box 34

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in RNA processing IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in nucleolus IEA
Inferred from Electronic Annotation
more info
 

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.

RNA

  1. NR_002968.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AJ609443
    Related
    ENST00000408564.2

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    48654382..48654518 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    48616405..48616541 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)