SNORA87

Summary

SNORA87 (small nucleolar RNA, H/ACA box 87, HGNC:50391) is a gene on chromosome 10q25.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50391
Approved symbol	SNORA87
Name	small nucleolar RNA, H/ACA box 87
Location	10q25.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635520
RNAcentral	URS00008E3A56 — snoRNA, 222 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): RS1000006717 (10:113045628 A>G), RS1000625180 (10:113045932 C>T), RS1001444195 (10:113044760 C>G,T), RS1002853012 (10:113043423 C>A), RS1003126250 (10:113043615 C>G), RS1004303654 (10:113045689 G>T), RS1005638860 (10:113045014 G>T), RS1006388533 (10:113043830 A>G), RS1007081043 (10:113044102 T>C), RS1007203424 (10:113043726 CTT>C,CTTT), RS1007438373 (10:113044397 T>C), RS1010381048 (10:113043907 A>G), RS1010901841 (10:113044090 T>C), RS1011485760 (10:113043623 A>G), RS1013576616 (10:113044834 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.