SNORD150

Summary

SNORD150 (small nucleolar RNA, C/D box 150, HGNC:51864) is a gene on chromosome 11q23.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51864
Approved symbol	SNORD150
Name	small nucleolar RNA, C/D box 150
Location	11q23.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623467
RNAcentral	URS0000ABD875 — snoRNA, 75 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): RS1000176398 (11:119190517 T>C), RS1002195650 (11:119192461 T>C), RS1004800970 (11:119192417 A>T), RS1005869242 (11:119191084 C>T), RS1007094130 (11:119191435 CAG>C), RS1007681613 (11:119191756 C>A,T), RS1008341396 (11:119191341 G>A), RS1011193570 (11:119190187 TAAATAAAAATAA>T,TAAATAA,TAAATAAAAATAAAAATAA), RS1012365154 (11:119190520 G>A,T), RS1012477787 (11:119190927 A>G), RS1014151387 (11:119192268 A>G), RS1014222699 (11:119192013 T>A,C), RS1014543470 (11:119191113 T>G), RS1014647836 (11:119190830 T>C), RS1018451406 (11:119191448 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.