SNORA118

Summary

SNORA118 (small nucleolar RNA, H/ACA box 118, HGNC:51856) is a gene on chromosome 19p13.11.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51856
Approved symbol	SNORA118
Name	small nucleolar RNA, H/ACA box 118
Location	19p13.11
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623483
RNAcentral	URS0000ABD8D8 — snoRNA, 131 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): RS1001190829 (19:17092741 A>C), RS1002185425 (19:17092662 T>A,C), RS1005421860 (19:17091067 C>T), RS1005524745 (19:17091479 G>A), RS1006111927 (19:17092753 C>T), RS1008122495 (19:17090381 G>A), RS1008571414 (19:17090643 T>C), RS1009162128 (19:17092549 A>T), RS1009817136 (19:17091899 G>A), RS1009968198 (19:17092387 A>C), RS1011500164 (19:17090758 G>A,C,T), RS1011658517 (19:17090499 C>T), RS1012389140 (19:17091410 G>C), RS1012541552 (19:17091284 G>A), RS1014357070 (19:17091400 A>AT)

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.