SNORD128

Summary

SNORD128 (small nucleolar RNA, C/D box 128, HGNC:50409) is a gene on chromosome 1p36.23.

At a glance

• GWAS associations: 1

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50409
Approved symbol	SNORD128
Name	small nucleolar RNA, C/D box 128
Location	1p36.23
Locus type	RNA, small nucleolar
Status	Approved
Aliases	ZL43
Entrez	106632271
RNAcentral	URS00008E3A15 — snoRNA, 114 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): RS1000486159 (1:8496398 G>A,C), RS1002991018 (1:8496822 A>G), RS1005550987 (1:8494841 T>C), RS1005650549 (1:8494576 A>C), RS1006015773 (1:8494451 G>A,T), RS1007282504 (1:8495402 C>A), RS1007747060 (1:8495654 T>C), RS1007787278 (1:8496172 T>A,G), RS1008816009 (1:8496338 A>G,T), RS1009685485 (1:8496460 C>T), RS1010788714 (1:8495714 A>G), RS1012821920 (1:8494982 C>T), RS1013012367 (1:8496667 G>A), RS1014099041 (1:8495756 C>A), RS1014148333 (1:8496055 G>A,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

1 associations (top):

Study	Trait	p-value
GCST004521_274	Autism spectrum disorder or schizophrenia	7.000000e-09

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.