SNORD13I

Summary

SNORD13I (small nucleolar RNA, C/D box 13I, HGNC:52248) is a gene on chromosome 11q22.1.

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

Source: NCBI Gene 109616988 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52248
Approved symbol	SNORD13I
Name	small nucleolar RNA, C/D box 13I
Location	11q22.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109616988
RNAcentral	URS00006868FF — snoRNA, 105 nt, 3 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): RS1000279623 (11:100934118 C>A), RS1001083722 (11:100932405 A>C,G), RS1002022270 (11:100934316 A>G,T), RS1002543015 (11:100934073 A>G), RS1003790962 (11:100933346 G>A), RS1005653083 (11:100933294 A>C,G), RS1005911519 (11:100934009 A>T), RS1005990276 (11:100933747 C>T), RS1006684665 (11:100934423 T>A), RS1009854593 (11:100932831 G>A,C), RS1010793769 (11:100934651 A>G), RS1010823290 (11:100934335 C>T), RS1014170274 (11:100932332 T>C), RS1015770084 (11:100932960 G>C), RS1017121959 (11:100934770 C>A,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.