SNORD141A

Summary

SNORD141A (small nucleolar RNA, C/D box 141A, HGNC:51406) is a gene on chromosome 9q34.13.

At a glance

• GWAS associations: 1

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51406
Approved symbol	SNORD141A
Name	small nucleolar RNA, C/D box 141A
Location	9q34.13
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635683
RNAcentral	URS00008E397A — 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): RS1003235063 (9:133018904 G>A,T), RS1003284164 (9:133019128 A>G), RS1008595829 (9:133018800 G>A), RS1015955837 (9:133018688 C>T), RS1017704115 (9:133019443 C>T), RS1018047643 (9:133020593 T>C), RS1022229806 (9:133019167 T>C,G), RS1025986238 (9:133018718 C>A,T), RS1029553090 (9:133019407 T>C), RS1031661633 (9:133018863 G>A), RS1031718313 (9:133019228 C>A,T), RS1037959438 (9:133019079 C>T), RS1040037123 (9:133019075 T>A,C), RS1043476159 (9:133020358 T>G), RS1044601990 (9:133018719 G>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

1 associations (top):

Study	Trait	p-value
GCST005990_49	Non-albumin protein levels	2.000000e-08

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Smoke	decreases expression	1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.