SNORD153

Summary

SNORD153 (small nucleolar RNA, C/D box 153, HGNC:51867) is a gene on chromosome 11q25.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51867
Approved symbol	SNORD153
Name	small nucleolar RNA, C/D box 153
Location	11q25
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623486
RNAcentral	URS0000ABD845 — snoRNA, 76 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): RS1000042481 (11:134152110 G>A,C), RS1001202097 (11:134151854 C>T), RS1001335068 (11:134151931 G>A,T), RS1001422976 (11:134151688 T>G), RS1003550216 (11:134151019 A>C,G), RS1003771183 (11:134150842 G>C), RS1004892103 (11:134152469 C>G), RS1004997776 (11:134153132 A>G), RS1005415449 (11:134152646 C>A,T), RS1006006558 (11:134152389 T>A,C), RS1006010382 (11:134151639 C>T), RS1006072814 (11:134151436 T>C,G), RS1006414511 (11:134152525 ATAT>A,ATATTAT), RS1007985693 (11:134152353 T>TAAC), RS1008575588 (11:134151388 C>A,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.