SNORD170

Summary

SNORD170 (small nucleolar RNA, C/D box 170, HGNC:51884) is a gene on chromosome 5p15.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51884
Approved symbol	SNORD170
Name	small nucleolar RNA, C/D box 170
Location	5p15.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623458
RNAcentral	URS0000ABD7F6 — snoRNA, 85 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): RS1001368447 (5:14462060 C>T), RS1001795357 (5:14462296 T>C,G), RS1003370890 (5:14462716 G>A), RS1003897152 (5:14464114 C>T), RS1003929909 (5:14464359 T>C), RS1004112690 (5:14463287 A>G), RS1005655047 (5:14463395 A>G), RS1007156359 (5:14463752 CT>C), RS1008257886 (5:14462703 A>T), RS1008284970 (5:14462976 G>A,T), RS1009740416 (5:14463260 T>A,C,G), RS1011255662 (5:14462444 A>G), RS1012640547 (5:14463724 C>G,T), RS1013353476 (5:14464193 G>A,T), RS1013435822 (5:14462807 C>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.