SNORD166

Summary

SNORD166 (small nucleolar RNA, C/D box 166, HGNC:51880) is a gene on chromosome 6q21.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51880
Approved symbol	SNORD166
Name	small nucleolar RNA, C/D box 166
Location	6q21
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623478
RNAcentral	URS0000ABD89C — snoRNA, 106 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): RS1001252669 (6:111113239 T>C), RS1001810018 (6:111112912 A>G), RS1003747168 (6:111114237 G>A), RS1005162245 (6:111112112 C>T), RS1007958078 (6:111113656 G>A,C), RS1009348886 (6:111114100 G>A), RS1011454853 (6:111113595 T>C), RS1013707594 (6:111112456 T>C), RS1014523408 (6:111113061 T>C), RS1016185955 (6:111113938 G>A), RS1016343497 (6:111113674 G>C), RS1016544791 (6:111112478 G>A), RS1020236049 (6:111113418 T>G), RS1020309986 (6:111113014 A>G), RS1023819874 (6:111112207 AT>A,ATT,ATTTTTT)

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.