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

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

Location:: Xq28

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	X	NC_000023.11 (154768528..154768659)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	X	NC_060947.1 (153004938..153005069)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	X	NC_000023.10 (153996803..153996934)

Chromosome X - NC_000023.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

stSG604277 (e-PCR)
- UniSTS:447594

ECD10168 (e-PCR)
- UniSTS:291208

REN90596 (e-PCR)
- UniSTS:415394

REN90597 (e-PCR)
- UniSTS:415395

REN90598 (e-PCR)
- UniSTS:415396

REN90599 (e-PCR)
- UniSTS:415397

REN90600 (e-PCR)
- UniSTS:415398

REN90601 (e-PCR)
- UniSTS:415399

REN90602 (e-PCR)
- UniSTS:415400

REN90603 (e-PCR)
- UniSTS:415401

REN90604 (e-PCR)
- UniSTS:415402

REN90605 (e-PCR)
- UniSTS:415403

ECD09694 (e-PCR)
- UniSTS:290735

ECD14101 (e-PCR)
- UniSTS:295126

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.