SNORD129

Summary

SNORD129 (small nucleolar RNA, C/D box 129, HGNC:50410) is a gene on chromosome 10p14.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50410
Approved symbol	SNORD129
Name	small nucleolar RNA, C/D box 129
Location	10p14
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635547
RNAcentral	URS00008E39EC — snoRNA, 105 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): RS1001056650 (10:7188486 G>A,T), RS1001143107 (10:7188298 G>A), RS1002149423 (10:7186875 A>T), RS1004770446 (10:7187911 C>A,T), RS1004898470 (10:7188574 A>C,T), RS1005848191 (10:7187621 T>C), RS1005952118 (10:7187190 G>A), RS1009118853 (10:7186463 T>C), RS1009736125 (10:7188281 T>C), RS1010382876 (10:7187066 T>C), RS1010750622 (10:7186500 A>G,T), RS1011388547 (10:7188454 G>A,C), RS1011711968 (10:7188162 C>G,T), RS1013598476 (10:7188315 A>G), RS1014728379 (10:7187578 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.