SNORA92

Summary

SNORA92 (small nucleolar RNA, H/ACA box 92, HGNC:50396) is a gene on chromosome 22q13.1.

At a glance

• Clinical variants (ClinVar): 1 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50396
Approved symbol	SNORA92
Name	small nucleolar RNA, H/ACA box 92
Location	22q13.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635525
RNAcentral	URS00008E398A — snoRNA, 242 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

1 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000754071 (22:38224726 G>A,T), RS1001227287 (22:38224945 G>A), RS1002366486 (22:38225845 A>C,G), RS1002948785 (22:38226628 T>C), RS1003298083 (22:38224701 G>C), RS1006536534 (22:38226482 C>T), RS1006796699 (22:38224113 TTTTC>T), RS1008547467 (22:38225942 G>A), RS1009409807 (22:38225223 T>C), RS1011020059 (22:38224447 G>C), RS1013760914 (22:38224305 A>G), RS1013776523 (22:38226031 AGT>A), RS1014162009 (22:38226331 T>C), RS1015309467 (22:38224550 C>G,T), RS1015874989 (22:38225890 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Aflatoxin B1	decreases methylation	1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.