SNORA111

Summary

SNORA111 (small nucleolar RNA, H/ACA box 111, HGNC:51404) is a gene on chromosome 18q12.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51404
Approved symbol	SNORA111
Name	small nucleolar RNA, H/ACA box 111
Location	18q12.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635546
RNAcentral	URS00008E3987 — snoRNA, 166 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): RS1000021963 (18:37468228 G>A), RS1000201677 (18:37468035 C>T), RS1001621338 (18:37465953 T>C), RS1002066506 (18:37467095 C>A,T), RS1002148576 (18:37466860 A>C), RS1004461442 (18:37468343 C>A), RS1006302810 (18:37466644 G>T), RS1006524281 (18:37468458 G>A), RS1008708539 (18:37467692 C>T), RS1010387904 (18:37466283 C>T), RS1010458414 (18:37466569 G>T), RS1011237649 (18:37467702 C>G), RS1013335550 (18:37465890 G>A), RS1013348687 (18:37466933 C>G,T), RS1013439070 (18:37468258 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.