SNORD160

Summary

SNORD160 (small nucleolar RNA, C/D box 160, HGNC:51874) is a gene on chromosome 1p34.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51874
Approved symbol	SNORD160
Name	small nucleolar RNA, C/D box 160
Location	1p34.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623476
RNAcentral	URS0000ABD889 — snoRNA, 73 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): RS1003738801 (1:44761465 A>G), RS1003993670 (1:44760953 C>T), RS1005766399 (1:44761505 G>A), RS1005818523 (1:44761661 A>G), RS1007248035 (1:44761093 A>G), RS1009239685 (1:44761116 G>A,T), RS1014154977 (1:44761974 A>G), RS1014503085 (1:44762186 G>A,C), RS1017224637 (1:44761671 T>C), RS1017457413 (1:44761805 G>A), RS1018342756 (1:44762276 G>C,T), RS1019257203 (1:44761251 T>G), RS1019356473 (1:44760972 G>C), RS1022078812 (1:44762282 G>T), RS1023665992 (1:44760649 C>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.