SNORA120

Summary

SNORA120 (small nucleolar RNA, H/ACA box 120, HGNC:51858) is a gene on chromosome 12p13.31.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51858
Approved symbol	SNORA120
Name	small nucleolar RNA, H/ACA box 120
Location	12p13.31
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109729112
RNAcentral	URS0000ABD83F — snoRNA, 147 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): RS1002414137 (12:6039588 T>C), RS1002614297 (12:6040976 C>T), RS1002674362 (12:6040978 G>A,C), RS1002747694 (12:6040772 G>A), RS1003846978 (12:6041375 A>G), RS1004324792 (12:6041152 G>A,C,T), RS1008854886 (12:6042085 CAT>C), RS1008937318 (12:6039999 C>T), RS1009278418 (12:6040215 C>A,T), RS1009832038 (12:6041273 T>C), RS1010209076 (12:6039640 TAAGC>T), RS1011719448 (12:6041621 T>C), RS1012222661 (12:6041792 C>T), RS1012892539 (12:6041900 G>A), RS1012994096 (12:6042181 A>G)

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.