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SNORA36A small nucleolar RNA, H/ACA box 36A [ Homo sapiens (human) ]

Gene ID: 677817, updated on 13-May-2022

Summary

Official Symbol
SNORA36Aprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 36Aprovided by HGNC
Primary source
HGNC:HGNC:32628
See related
Ensembl:ENSG00000206948 AllianceGenome:HGNC:32628
Gene type
snoRNA
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ACA36
Summary
Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residues U105 and U1244 of 18S rRNA. [provided by RefSeq, Feb 2009]
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Genomic context

See SNORA36A in Genome Data Viewer
Location:
Xq28
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (154768528..154768659)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (153004938..153005069)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (153996803..153996934)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 3 subfamily B member 1 pseudogene Neighboring gene GRB2 associated binding protein 3 Neighboring gene Sharpr-MPRA regulatory region 12525 Neighboring gene microRNA 664b Neighboring gene dyskerin pseudouridine synthase 1 Neighboring gene small nucleolar RNA, H/ACA box 56 Neighboring gene MAGUK p55 scaffold protein 1

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ACA36 snoRNA

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_002969.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AJ609463
    Related
    ENST00000384221.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    154768528..154768659
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    153004938..153005069
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)