SNORD154

Summary

SNORD154 (small nucleolar RNA, C/D box 154, HGNC:51868) is a gene on chromosome 20q12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51868
Approved symbol	SNORD154
Name	small nucleolar RNA, C/D box 154
Location	20q12
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623474
RNAcentral	URS0000ABD89B — snoRNA, 52 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): RS1000957964 (20:40714295 G>A,T), RS1002563396 (20:40715963 A>G), RS1002667905 (20:40716495 G>A), RS1002919596 (20:40716265 T>C), RS1007183271 (20:40715617 A>G), RS1007881496 (20:40714519 G>A), RS1008180995 (20:40714335 G>A), RS1009871076 (20:40716542 A>C), RS1012540593 (20:40716288 G>T), RS1012654782 (20:40716598 C>A), RS1013514388 (20:40714925 C>T), RS1015084170 (20:40714200 G>A), RS1016618288 (20:40715981 A>G), RS1016651213 (20:40716285 C>T), RS1018762501 (20:40715502 G>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.