SNORD169

Summary

SNORD169 (small nucleolar RNA, C/D box 169, HGNC:51883) is a gene on chromosome 14q24.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51883
Approved symbol	SNORD169
Name	small nucleolar RNA, C/D box 169
Location	14q24.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623479
RNAcentral	URS0000ABD8CD — snoRNA, 64 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): RS1000593332 (14:69976268 C>T), RS1001000286 (14:69976478 A>G), RS1003542088 (14:69978466 A>C,G), RS1004560916 (14:69976901 G>A), RS1008680749 (14:69977443 C>T), RS1008739109 (14:69977172 C>G), RS1009567303 (14:69976691 C>T), RS1011573047 (14:69977894 T>A,C), RS1012653977 (14:69977768 A>G,T), RS1012954497 (14:69977072 C>A,T), RS1015525493 (14:69976451 C>T), RS1016150647 (14:69976906 A>G,T), RS1019464214 (14:69977596 G>A,C,T), RS1021112720 (14:69976242 A>G), RS1023375578 (14:69978414 C>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.