SNORA88

Summary

SNORA88 (small nucleolar RNA, H/ACA box 88, HGNC:50392) is a gene on chromosome 11p13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50392
Approved symbol	SNORA88
Name	small nucleolar RNA, H/ACA box 88
Location	11p13
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635521
RNAcentral	URS00008E3A21 — snoRNA, 171 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): RS1000558203 (11:32144342 C>T), RS1000930222 (11:32144149 C>G,T), RS1001739146 (11:32145282 C>G), RS1001770217 (11:32145499 C>T), RS1002439830 (11:32143783 GT>G), RS1005417541 (11:32144099 A>T), RS1005495075 (11:32144287 T>G), RS1007078602 (11:32144154 AGCTGGGACTACAGGT>A), RS1007543213 (11:32144979 A>C,T), RS1008825484 (11:32143495 T>A), RS1010758878 (11:32145659 T>TC), RS1011221740 (11:32143581 C>T), RS1011359761 (11:32143300 T>C), RS1012682181 (11:32144025 T>G), RS1012816682 (11:32143637 A>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.