SNORA90

Summary

SNORA90 (small nucleolar RNA, H/ACA box 90, HGNC:50394) is a gene on chromosome 17q12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50394
Approved symbol	SNORA90
Name	small nucleolar RNA, H/ACA box 90
Location	17q12
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635523
RNAcentral	URS00008E39A2 — snoRNA, 175 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

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): RS1001202288 (17:37244051 CT>C), RS1002547954 (17:37243643 G>A), RS1003843705 (17:37243704 C>A,T), RS1004320042 (17:37244008 A>G), RS1004743785 (17:37242818 C>G), RS1008167141 (17:37244237 G>A,T), RS1009379522 (17:37243306 G>A), RS1009836398 (17:37244351 G>A), RS1010141874 (17:37243745 T>A,C), RS1010778608 (17:37243624 T>C,G), RS1011346041 (17:37243020 T>C), RS1013773171 (17:37243884 T>C), RS1015203741 (17:37244009 T>C), RS1015336504 (17:37243738 T>C), RS1019093241 (17:37244295 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

Clinical trials (associated diseases)

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