SNORD168

Summary

SNORD168 (small nucleolar RNA, C/D box 168, HGNC:51882) is a gene on chromosome 8q24.11.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51882
Approved symbol	SNORD168
Name	small nucleolar RNA, C/D box 168
Location	8q24.11
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623457
RNAcentral	URS0000ABD882 — 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): RS1000850005 (8:117920646 T>C), RS1001090081 (8:117920957 C>G), RS1001862222 (8:117922400 T>G), RS1001905719 (8:117921562 C>CA), RS1002274584 (8:117921298 T>C), RS1006218084 (8:117922867 T>G), RS1007647566 (8:117921378 G>C), RS1007947244 (8:117922491 G>A), RS1008023525 (8:117922219 C>G), RS1008614985 (8:117920595 G>A,T), RS1009609576 (8:117920657 T>C,G), RS1009857750 (8:117922430 T>C), RS1009950707 (8:117922221 C>A), RS1014258693 (8:117920367 G>A), RS1014473449 (8:117921628 T>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.