SNORD165

Summary

SNORD165 (small nucleolar RNA, C/D box 165, HGNC:51879) is a gene on chromosome 7p22.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51879
Approved symbol	SNORD165
Name	small nucleolar RNA, C/D box 165
Location	7p22.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623455
RNAcentral	URS0000ABD87E — snoRNA, 63 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): RS1000083275 (7:4837528 C>A,G), RS1000296583 (7:4837110 T>G), RS1000388775 (7:4839129 G>A), RS1000410880 (7:4836967 G>A), RS1003770417 (7:4839057 G>A), RS1004485420 (7:4838735 C>T), RS1004936412 (7:4839070 C>G,T), RS1005104476 (7:4837716 G>A), RS1006545483 (7:4837239 A>G), RS1006564392 (7:4837052 G>A), RS1008282483 (7:4838694 A>G), RS1009681901 (7:4837158 C>G), RS1010282881 (7:4839402 T>C), RS1011203868 (7:4837252 G>A), RS1011256134 (7:4837467 T>C)

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.