SNORD151

Summary

SNORD151 (small nucleolar RNA, C/D box 151, HGNC:51865) is a gene on chromosome 7p12.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51865
Approved symbol	SNORD151
Name	small nucleolar RNA, C/D box 151
Location	7p12.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623468
RNAcentral	URS0000ABD894 — snoRNA, 84 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): RS1000867649 (7:47465763 A>G), RS1002993781 (7:47466015 A>G), RS1003289610 (7:47464983 G>A,T), RS1003320793 (7:47464617 C>T), RS1004159402 (7:47465663 G>A), RS1004270794 (7:47466392 T>G), RS1004429149 (7:47465425 T>C,G), RS1006658630 (7:47464635 A>G), RS1007844249 (7:47465895 G>T), RS1010165791 (7:47465818 G>A), RS1010685013 (7:47465310 T>C), RS1010731107 (7:47466757 G>A), RS1010766065 (7:47466537 G>A), RS1010967380 (7:47465018 T>C), RS1013060581 (7:47464565 G>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.