SNORD158

Summary

SNORD158 (small nucleolar RNA, C/D box 158, HGNC:51872) is a gene on chromosome 10q25.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51872
Approved symbol	SNORD158
Name	small nucleolar RNA, C/D box 158
Location	10q25.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623470
RNAcentral	URS0000ABD803 — snoRNA, 58 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): RS1003863896 (10:116194713 T>A), RS1006447949 (10:116194958 G>A,T), RS1006564803 (10:116195500 T>C), RS1007659275 (10:116195431 G>A), RS1008236438 (10:116196438 G>A), RS1010641543 (10:116194752 C>T), RS1012339191 (10:116195948 G>A,C), RS1015344885 (10:116196499 TATATATA>T), RS1016358055 (10:116194965 G>A), RS1016411920 (10:116194703 A>C), RS1017625739 (10:116195165 A>G), RS1017887903 (10:116195195 A>C,T), RS1019049379 (10:116196510 T>C), RS1022057299 (10:116194374 G>A,C), RS1023775770 (10:116194477 T>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.