SNORD13F

Summary

SNORD13F (small nucleolar RNA, C/D box 13F, HGNC:52245) is a gene on chromosome 11q13.1.

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

Source: NCBI Gene 109616986 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52245
Approved symbol	SNORD13F
Name	small nucleolar RNA, C/D box 13F
Location	11q13.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109616986
RNAcentral	URS000065912C — snoRNA, 85 nt, 5 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): RS1001111307 (11:66051798 C>T), RS1002167154 (11:66052077 C>A), RS1002283364 (11:66051871 A>C,G), RS1003394196 (11:66053146 C>A,G,T), RS1004288347 (11:66052255 G>A,C), RS1007416265 (11:66052515 A>T), RS1008184435 (11:66051868 A>G), RS1009255157 (11:66052750 G>A), RS1009884945 (11:66052931 A>T), RS1010557735 (11:66053503 ACT>A), RS1010693641 (11:66053107 A>C,G), RS1012154470 (11:66053628 C>A,T), RS1013817021 (11:66052026 G>A,C), RS1013906849 (11:66051290 G>C), RS1014741773 (11:66052104 G>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.