SNORA119

Summary

SNORA119 (small nucleolar RNA, H/ACA box 119, HGNC:51857) is a gene on chromosome 16q24.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51857
Approved symbol	SNORA119
Name	small nucleolar RNA, H/ACA box 119
Location	16q24.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623464
RNAcentral	URS0000ABD8B9 — snoRNA, 144 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): RS1000403224 (16:89952085 G>C), RS1001946770 (16:89952119 C>T), RS1002169094 (16:89951687 C>T), RS1002851519 (16:89953698 G>A), RS1003584018 (16:89952413 A>G), RS1004788178 (16:89953033 A>G), RS1005009264 (16:89953966 G>A), RS1005058100 (16:89953748 G>A), RS1005726970 (16:89951770 C>G), RS1008523539 (16:89954010 T>C), RS1009189166 (16:89951996 G>A,C), RS1009756641 (16:89952218 T>C), RS1009807177 (16:89952093 G>A), RS1010147413 (16:89953016 C>A), RS1010399167 (16:89952367 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

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
aflatoxin B2	decreases methylation	1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.