SNORA93

Summary

SNORA93 (small nucleolar RNA, H/ACA box 93, HGNC:50397) is a gene on chromosome 3p25.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50397
Approved symbol	SNORA93
Name	small nucleolar RNA, H/ACA box 93
Location	3p25.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635526
RNAcentral	URS00008E3A7A — snoRNA, 168 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

Literature-anchored findings (GeneRIF, showing 1)

• Tumor-educated platelet SNORA58, SNORA68 and SNORD93 as novel diagnostic biomarkers for esophageal cancer. (PMID:37129021)

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

0 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): RS1001412948 (3:13618918 C>A,T), RS1001590971 (3:13618680 C>G,T), RS1002019784 (3:13618431 A>G), RS1002474796 (3:13617183 C>T), RS1004388930 (3:13617483 C>T), RS1004433396 (3:13617941 G>C), RS1004944341 (3:13616431 C>G), RS1006007588 (3:13617444 A>T), RS1008119670 (3:13616502 G>A), RS1009723752 (3:13617362 C>G), RS1009786181 (3:13616762 G>C,T), RS1010134721 (3:13617661 A>C,G), RS1010287644 (3:13618574 C>A,G,T), RS1010757885 (3:13618895 C>T), RS1010779879 (3:13618775 C>T)

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

Clinical trials (associated diseases)

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