SNORD161

Summary

SNORD161 (small nucleolar RNA, C/D box 161, HGNC:51875) is a gene on chromosome 4q21.21.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51875
Approved symbol	SNORD161
Name	small nucleolar RNA, C/D box 161
Location	4q21.21
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623453
RNAcentral	URS0000ABD844 — snoRNA, 66 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): RS1001763453 (4:78287648 T>C), RS10023496 (4:78289275 T>C,G), RS1002568228 (4:78289294 A>G), RS10028695 (4:78288976 G>A,T), RS1005051797 (4:78287914 A>G), RS1005912230 (4:78287239 C>A,G,T), RS1006379038 (4:78287581 G>A), RS1006594983 (4:78288297 G>A), RS1007376804 (4:78287640 T>A), RS1007429340 (4:78287892 T>A), RS1009096211 (4:78289366 T>A), RS1009378286 (4:78287901 T>C), RS1009840839 (4:78288240 T>G), RS1009887100 (4:78288564 A>G), RS1009902454 (4:78288786 T>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.