SNORA114

Summary

SNORA114 (small nucleolar RNA, H/ACA box 114, HGNC:51852) is a gene on chromosome 7p22.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51852
Approved symbol	SNORA114
Name	small nucleolar RNA, H/ACA box 114
Location	7p22.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623488
RNAcentral	URS0000ABD8BD — snoRNA, 141 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): RS1000230409 (7:2089571 C>T), RS1001082752 (7:2090923 T>C), RS1002702133 (7:2090864 G>C), RS1002734527 (7:2091052 A>G), RS1003744762 (7:2090117 G>A), RS1004980342 (7:2090942 A>C), RS1004988922 (7:2090489 G>A,C), RS1005344889 (7:2090716 G>A,C), RS1006228333 (7:2090209 G>A), RS1007426317 (7:2088916 T>A), RS1008324090 (7:2088466 C>G), RS1008614759 (7:2089696 G>A,T), RS1008687624 (7:2088638 C>A), RS1009075571 (7:2089493 C>T), RS1009792576 (7:2088492 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.