SNORD3K

Summary

SNORD3K (small nucleolar RNA, C/D box 3K, HGNC:52244) is a gene on chromosome 2q31.1.

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

Source: NCBI Gene 109617017 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52244
Approved symbol	SNORD3K
Name	small nucleolar RNA, C/D box 3K
Location	2q31.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109617017
RNAcentral	URS0000A95150 — snoRNA, 100 nt, 1 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): RS1002614982 (2:169816795 C>G), RS1003418008 (2:169815233 T>C), RS1004424138 (2:169814970 C>T), RS1004662290 (2:169814355 T>C,G), RS1004713218 (2:169814916 T>C), RS1006338731 (2:169815975 G>A), RS1006417292 (2:169816771 C>T), RS1007843044 (2:169815896 C>T), RS1007979709 (2:169814282 T>C), RS1010469671 (2:169815624 A>T), RS1010797863 (2:169815845 T>G), RS1013696743 (2:169816747 C>T), RS1014018243 (2:169816455 T>G), RS1015008694 (2:169816010 A>G), RS1015018800 (2:169816379 T>C)

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.