SNORA113

Summary

SNORA113 (small nucleolar RNA, H/ACA box 113, HGNC:51851) is a gene on chromosome 12q15.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51851
Approved symbol	SNORA113
Name	small nucleolar RNA, H/ACA box 113
Location	12q15
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623461
RNAcentral	URS0000ABD847 — snoRNA, 154 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): RS1000003443 (12:69515133 A>G), RS1000438263 (12:69514726 A>G), RS1002074940 (12:69513583 G>A), RS1002831590 (12:69514484 A>T), RS1004690216 (12:69514407 G>A), RS1005935470 (12:69513984 C>T), RS1006865605 (12:69515572 CTG>C), RS1008385577 (12:69516075 T>C,G), RS1010197367 (12:69514693 C>T), RS1011492316 (12:69515196 G>A), RS1014048290 (12:69515585 T>A), RS1016449244 (12:69515761 A>G), RS1016569679 (12:69513705 A>T), RS1018302858 (12:69514045 A>T), RS1018672383 (12:69513692 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

Clinical trials (associated diseases)

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