SNORD133

Summary

SNORD133 (small nucleolar RNA, C/D box 133, HGNC:50414) is a gene on chromosome 12q13.12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50414
Approved symbol	SNORD133
Name	small nucleolar RNA, C/D box 133
Location	12q13.12
Locus type	RNA, small nucleolar
Status	Approved
Aliases	ZL42, ggn68
Entrez	106633800
RNAcentral	URS00008E3A5F — snoRNA, 216 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): RS1002445217 (12:50457044 C>T), RS1002474406 (12:50455491 A>T), RS1003409094 (12:50455910 G>T), RS1003442136 (12:50455709 A>T), RS1004255565 (12:50455388 A>G), RS1004511326 (12:50456755 G>T), RS1005022587 (12:50455241 G>A,C), RS1008250936 (12:50454631 A>G), RS1008589184 (12:50456025 C>T), RS1008885346 (12:50457011 C>A), RS1008917991 (12:50456645 T>G), RS1010647313 (12:50455515 T>G), RS1011370006 (12:50457106 G>C), RS1014751078 (12:50456123 C>T), RS1018345893 (12:50454641 T>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.