SNORA86

Summary

SNORA86 (small nucleolar RNA, H/ACA box 86, HGNC:50390) is a gene on chromosome 10p11.22.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50390
Approved symbol	SNORA86
Name	small nucleolar RNA, H/ACA box 86
Location	10p11.22
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106633814
RNAcentral	URS00008E3A3E — snoRNA, 139 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): RS1000222337 (10:32902394 A>G), RS1000505816 (10:32903295 T>G), RS1004463134 (10:32903401 A>G), RS1004688066 (10:32903082 T>A), RS1005702366 (10:32902322 C>A), RS1006599928 (10:32901854 G>A), RS1008263917 (10:32903108 T>C), RS1010322106 (10:32902729 T>C), RS1010622368 (10:32903072 G>A,T), RS1013601446 (10:32902453 A>G), RS1016703578 (10:32901087 T>C), RS1018379998 (10:32902814 G>A), RS1019097334 (10:32901599 C>T), RS1019383258 (10:32902884 T>C), RS1022971853 (10:32901661 A>G)

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.