SNORD3I

Summary

SNORD3I (small nucleolar RNA, C/D box 3I, HGNC:52242) is a gene on chromosome 8p23.1.

Predicted to be involved in RNA processing. Predicted to be located in nucleolus.

Source: NCBI Gene 109616996 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52242
Approved symbol	SNORD3I
Name	small nucleolar RNA, C/D box 3I
Location	8p23.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109616996
RNAcentral	URS0000ABD8AD — snoRNA, 92 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): RS1000603907 (8:9060603 C>G), RS1001063343 (8:9058854 T>TA), RS1002015266 (8:9059853 G>A), RS1002080015 (8:9058922 G>A), RS1004576216 (8:9059039 G>A), RS1004626927 (8:9058937 C>A,G), RS1005999961 (8:9058568 T>C), RS1007848726 (8:9060170 A>G), RS1008473863 (8:9058603 C>T), RS1008526012 (8:9058319 G>C,T), RS1008799319 (8:9059292 G>A), RS1008859776 (8:9059123 G>A), RS1008988104 (8:9059381 T>G), RS1009307572 (8:9059502 G>C), RS1009525428 (8:9059570 A>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.