SNORA94

Summary

SNORA94 (small nucleolar RNA, H/ACA box 94, HGNC:50398) is a gene on chromosome 3p21.31.

At a glance

• Clinical variants (ClinVar): 1 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50398
Approved symbol	SNORA94
Name	small nucleolar RNA, H/ACA box 94
Location	3p21.31
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635528
RNAcentral	URS00008E39F0 — snoRNA, 231 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): RS1002746804 (3:48606887 G>A,C), RS1003721234 (3:48605019 G>A,C), RS1003935835 (3:48606680 G>A), RS1006453977 (3:48606529 A>C), RS1007620732 (3:48606024 G>C), RS1008129719 (3:48606305 G>A), RS1010557199 (3:48605219 C>A), RS1011812146 (3:48605591 C>G), RS1012145225 (3:48606932 T>A,C), RS1012362353 (3:48604960 A>C), RS1012393391 (3:48605179 C>T), RS1017516858 (3:48605673 C>A,G), RS1017574515 (3:48606027 A>C), RS1017796015 (3:48606974 T>C), RS1018704608 (3:48605668 C>G,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.