SNORA117

Summary

SNORA117 (small nucleolar RNA, H/ACA box 117, HGNC:51855) is a gene on chromosome 20q13.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51855
Approved symbol	SNORA117
Name	small nucleolar RNA, H/ACA box 117
Location	20q13.33
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623463
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): RS1000612406 (20:62883183 CA>C), RS1000898893 (20:62883531 G>A,C), RS1000950579 (20:62883323 C>T), RS1002133198 (20:62882839 C>T), RS1002136517 (20:62883125 T>C), RS1002201007 (20:62883811 G>A,T), RS1002529632 (20:62882886 G>C), RS1003861994 (20:62884814 ACTCT>A,ACT), RS1005029547 (20:62883726 G>A), RS1005278299 (20:62882984 G>A), RS1005371370 (20:62882805 G>A), RS1006639563 (20:62883692 G>A), RS1006890344 (20:62884232 CA>C), RS1006994764 (20:62882578 C>A,T), RS1008759440 (20:62884584 G>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.