SNORD155

Summary

SNORD155 (small nucleolar RNA, C/D box 155, HGNC:51869) is a gene on chromosome 3q13.31.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51869
Approved symbol	SNORD155
Name	small nucleolar RNA, C/D box 155
Location	3q13.31
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623450
RNAcentral	URS0000ABD7F8 — snoRNA, 61 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): RS1002616263 (3:115906263 T>G), RS1002953676 (3:115905501 A>G), RS1006424801 (3:115906904 T>C), RS1006550418 (3:115905565 G>A,C), RS1007189881 (3:115905770 A>G), RS1008189207 (3:115906525 G>A), RS1008220035 (3:115907086 C>A,G), RS1009966389 (3:115904642 T>C), RS1010372169 (3:115905813 A>G,T), RS1015791438 (3:115905075 G>T), RS1016278267 (3:115904750 T>C), RS1017178577 (3:115905113 C>T), RS1017547776 (3:115904788 A>G), RS1018197957 (3:115906579 T>G), RS1020398665 (3:115906245 T>C)

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.