SNORA99

Summary

SNORA99 (small nucleolar RNA, H/ACA box 99, HGNC:50403) is a gene on chromosome 8p23.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50403
Approved symbol	SNORA99
Name	small nucleolar RNA, H/ACA box 99
Location	8p23.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635531
RNAcentral	URS00008E39B9 — snoRNA, 197 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): RS1000953343 (8:11705352 T>C), RS1001363463 (8:11705136 T>A), RS1001971008 (8:11704176 T>C), RS1002106624 (8:11705383 G>A), RS1002361227 (8:11704300 A>C,G), RS1002958031 (8:11703427 C>G,T), RS1003804474 (8:11704350 C>G), RS1004926174 (8:11703601 T>A,C), RS1005805259 (8:11704960 C>T), RS1005856138 (8:11704689 G>A,T), RS1006814457 (8:11705968 C>T), RS1007703424 (8:11704640 G>C), RS1008234077 (8:11704805 T>C), RS1008690347 (8:11703728 G>T), RS1008816021 (8:11703893 G>A,C,T)

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.