SNORD13G

Summary

SNORD13G (small nucleolar RNA, C/D box 13G, HGNC:52246) is a gene on chromosome 13q32.1.

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

Source: NCBI Gene 109616987 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52246
Approved symbol	SNORD13G
Name	small nucleolar RNA, C/D box 13G
Location	13q32.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109616987
RNAcentral	URS00006A860A — 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): RS1000944077 (13:95209443 G>A), RS1005787239 (13:95208672 G>A), RS1007535953 (13:95210252 G>A), RS1009466023 (13:95209726 A>G), RS1012849785 (13:95209299 T>C), RS1013158036 (13:95208815 T>C), RS1014091581 (13:95210117 T>C,G), RS1014621186 (13:95210306 C>G), RS1016089194 (13:95209805 C>A,T), RS1016119028 (13:95210044 T>C), RS1016354942 (13:95208688 T>A,C), RS1017092043 (13:95208383 C>A,T), RS1017123407 (13:95208690 G>A), RS1022765310 (13:95210585 C>A), RS1022835269 (13:95210322 TAAAA>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.