SNORA89

Summary

SNORA89 (small nucleolar RNA, H/ACA box 89, HGNC:50393) is a gene on chromosome 14q13.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50393
Approved symbol	SNORA89
Name	small nucleolar RNA, H/ACA box 89
Location	14q13.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635522
RNAcentral	URS00008E39EB — snoRNA, 177 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): RS1000360575 (14:33708827 A>G), RS1000391697 (14:33708570 A>C,G), RS1000574853 (14:33708212 A>G), RS1001568344 (14:33709311 T>C), RS1001939566 (14:33709145 C>A), RS1003829060 (14:33708515 C>T), RS1004641704 (14:33707653 G>A), RS1005602011 (14:33708850 A>C,T), RS1010431222 (14:33709142 C>T), RS1010496518 (14:33709533 G>A), RS1011670417 (14:33707182 A>G), RS1013234470 (14:33707908 C>T), RS1013515165 (14:33707700 G>A), RS1013702560 (14:33707683 A>T), RS1014293041 (14:33708869 T>C)

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.