SNORA112

Summary

SNORA112 (small nucleolar RNA, H/ACA box 112, HGNC:51850) is a gene on chromosome 2q11.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51850
Approved symbol	SNORA112
Name	small nucleolar RNA, H/ACA box 112
Location	2q11.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623481
RNAcentral	URS0000ABD8C0 — snoRNA, 124 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): RS1000539978 (2:96215032 G>C), RS1001059315 (2:96215210 G>A), RS1001488025 (2:96214251 C>A), RS1003592403 (2:96214005 A>T), RS1005200218 (2:96213207 G>A), RS1006252811 (2:96212964 A>G), RS1006962752 (2:96213291 G>A), RS1007996883 (2:96215011 C>G), RS1008485026 (2:96214791 G>A,T), RS1009321873 (2:96214712 T>G), RS1010891238 (2:96213133 C>G), RS1010922308 (2:96212715 C>T), RS1013580246 (2:96213897 A>C), RS1015845476 (2:96212980 C>G), RS1017263237 (2:96214254 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

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.