SNORD152

Summary

SNORD152 (small nucleolar RNA, C/D box 152, HGNC:51866) is a gene on chromosome 19q13.13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51866
Approved symbol	SNORD152
Name	small nucleolar RNA, C/D box 152
Location	19q13.13
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623473
RNAcentral	URS0000ABD890 — snoRNA, 54 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): RS1000897412 (19:38162129 C>T), RS1001284712 (19:38161905 G>T), RS1001909287 (19:38163163 A>T), RS1002643677 (19:38163581 G>A), RS1002981824 (19:38163309 G>A), RS1005931797 (19:38163294 A>C), RS1007147314 (19:38161176 T>A,C), RS1007161870 (19:38163630 G>A), RS1007740735 (19:38162606 C>T), RS1008866563 (19:38163216 G>A), RS1010169619 (19:38163332 A>G), RS1010551830 (19:38161933 T>C), RS1011142473 (19:38162957 C>T), RS1011585883 (19:38163198 A>G), RS1012740351 (19:38162191 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.