SNORA116

Summary

SNORA116 (small nucleolar RNA, H/ACA box 116, HGNC:51854) is a gene on chromosome 6q25.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51854
Approved symbol	SNORA116
Name	small nucleolar RNA, H/ACA box 116
Location	6q25.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623462
RNAcentral	URS0000ABD864 — snoRNA, 147 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): RS1000621156 (6:158321737 G>A), RS1000777916 (6:158321970 C>G), RS1002215745 (6:158322199 C>G), RS1002632928 (6:158321052 T>TA), RS1005190613 (6:158322938 C>T), RS1005241541 (6:158322537 C>A), RS1005298872 (6:158322995 T>C), RS1006299628 (6:158321479 G>A,C), RS1006691020 (6:158321717 T>C), RS1006742384 (6:158321988 C>G,T), RS1007099684 (6:158322314 A>G), RS1009038750 (6:158321008 C>T), RS1009194106 (6:158323529 T>C), RS1010168691 (6:158322131 G>C), RS1012536224 (6:158322969 C>T)

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.