SNORA110

Summary

SNORA110 (small nucleolar RNA, H/ACA box 110, HGNC:51403) is a gene on chromosome 1p34.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51403
Approved symbol	SNORA110
Name	small nucleolar RNA, H/ACA box 110
Location	1p34.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635545
RNAcentral	URS00008E3A22 — snoRNA, 216 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): RS1003024477 (1:44252577 T>C), RS1003461485 (1:44252971 C>T), RS1004988372 (1:44253365 G>C), RS1005057579 (1:44253736 A>G), RS1006235287 (1:44252993 C>T), RS1006592477 (1:44252524 A>C), RS1008131010 (1:44252177 G>C), RS1010298296 (1:44254487 T>TC), RS1011464352 (1:44254263 C>A), RS1014240209 (1:44252832 G>A), RS1014786302 (1:44253259 C>T), RS1016290786 (1:44253013 G>A), RS1016343557 (1:44253417 C>A), RS1018191130 (1:44253545 A>G), RS1019197614 (1:44253769 A>C)

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.