SNORD132

Summary

SNORD132 (small nucleolar RNA, C/D box 132, HGNC:50413) is a gene on chromosome 2q13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50413
Approved symbol	SNORD132
Name	small nucleolar RNA, C/D box 132
Location	2q13
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635550
RNAcentral	URS00008E3A41 — snoRNA, 100 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): RS1001354213 (2:110658565 T>A,C), RS1004041772 (2:110659673 T>C), RS1005764364 (2:110658150 T>C), RS1008345323 (2:110660227 T>C), RS1010021634 (2:110659010 G>C), RS1012912136 (2:110658932 G>A), RS1014565647 (2:110657985 T>C), RS1015901097 (2:110659847 T>C), RS1015958332 (2:110657956 C>T), RS1016662780 (2:110659446 G>A), RS1016907490 (2:110659588 T>C), RS1019955705 (2:110658636 G>A,C,T), RS1020450966 (2:110659041 C>T), RS1023583056 (2:110658979 T>C), RS1024532500 (2:110657791 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.