SNORD146

Summary

SNORD146 (small nucleolar RNA, C/D box 146, HGNC:51860) is a gene on chromosome 3p21.31.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51860
Approved symbol	SNORD146
Name	small nucleolar RNA, C/D box 146
Location	3p21.31
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623484
RNAcentral	URS0000ABD814 — snoRNA, 130 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): RS1000964489 (3:47662441 T>C), RS1002541105 (3:47663688 C>A,T), RS1004097725 (3:47662124 AGC>A), RS1005024681 (3:47662051 G>A,C), RS1005314336 (3:47663326 T>C,G), RS1006245017 (3:47663672 T>C,G), RS1006684046 (3:47663483 C>T), RS1008922164 (3:47661535 C>A,T), RS1009252672 (3:47663268 G>A,T), RS1012391025 (3:47661610 A>G,T), RS1013254743 (3:47662342 G>A), RS1014608666 (3:47662055 C>A), RS1014637877 (3:47661744 A>G), RS1016321913 (3:47663500 A>G), RS1016754857 (3:47663326 TAA>T,TA)

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.