SNORD162

Summary

SNORD162 (small nucleolar RNA, C/D box 162, HGNC:51876) is a gene on chromosome 4p16.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51876
Approved symbol	SNORD162
Name	small nucleolar RNA, C/D box 162
Location	4p16.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623454
RNAcentral	URS0000ABD855 — snoRNA, 98 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): RS1000517395 (4:4664696 G>C), RS1002089448 (4:4664151 C>T), RS1002286836 (4:4662786 G>A), RS1002426802 (4:4664347 A>G,T), RS1002721178 (4:4663034 T>A), RS1005327356 (4:4663818 G>A,T), RS1005360118 (4:4663637 C>A,T), RS1005378185 (4:4664125 G>A), RS1006879005 (4:4663435 C>T), RS1007480821 (4:4662360 A>G), RS1009252585 (4:4663999 T>C), RS1010495232 (4:4663410 T>C), RS1010930691 (4:4662733 C>T), RS1013281896 (4:4664672 C>G), RS1014173797 (4:4664390 G>A)

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.