SNORD13H

Summary

SNORD13H (small nucleolar RNA, C/D box 13H, HGNC:52247) is a gene on chromosome 16q22.1.

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

Source: NCBI Gene 109617018 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52247
Approved symbol	SNORD13H
Name	small nucleolar RNA, C/D box 13H
Location	16q22.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109617018
RNAcentral	URS0000729D3D — snoRNA, 104 nt, 4 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): RS1002833984 (16:69709342 A>G), RS1003069268 (16:69709642 A>C,G), RS1003498652 (16:69709135 G>A,T), RS1003770534 (16:69709568 T>A), RS10048108 (16:69708345 G>C,T), RS1007675593 (16:69708870 C>G), RS1008016956 (16:69708503 G>A,T), RS1008706115 (16:69710307 T>C), RS1008737189 (16:69710547 C>A), RS1009372295 (16:69708940 A>C), RS1010258103 (16:69710192 G>C), RS1010767751 (16:69709681 C>T), RS1011355370 (16:69708185 C>A), RS1011679085 (16:69708422 G>A), RS1014866579 (16:69710314 C>A)

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.