SNORD13C

Summary

SNORD13C (small nucleolar RNA, C/D box 13C, HGNC:52252) is a gene on chromosome 1q21.2.

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

Source: NCBI Gene 109616989 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52252
Approved symbol	SNORD13C
Name	small nucleolar RNA, C/D box 13C
Location	1q21.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109616989
RNAcentral	URS00006A4586 — snoRNA, 104 nt, 2 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): RS1004595135 (1:150259991 T>A), RS1009021861 (1:150261773 A>G), RS1013246713 (1:150261854 A>C), RS1025211854 (1:150260695 A>G), RS1027555162 (1:150261456 C>G), RS1029276281 (1:150260757 T>A), RS1032344208 (1:150260962 G>T), RS1033826118 (1:150260328 G>T), RS1034327050 (1:150260125 G>A), RS1036341669 (1:150262033 G>C), RS1037346169 (1:150260582 C>G,T), RS1037440315 (1:150260249 G>A,T), RS1038920169 (1:150259967 C>A,G,T), RS1042211548 (1:150259927 G>A), RS1046551228 (1:150261155 C>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.