SNORA98

Summary

SNORA98 (small nucleolar RNA, H/ACA box 98, HGNC:50402) is a gene on chromosome 6q24.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50402
Approved symbol	SNORA98
Name	small nucleolar RNA, H/ACA box 98
Location	6q24.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635530
RNAcentral	URS00008E3981 — snoRNA, 113 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): RS1000307470 (6:144405727 C>T), RS1001580039 (6:144404332 T>C), RS1002858671 (6:144404386 C>T), RS1003077374 (6:144404698 T>C), RS1004805604 (6:144405878 G>A), RS1004830333 (6:144406146 G>A), RS1005199513 (6:144405565 T>A,C), RS1006093647 (6:144404658 A>G), RS1006560748 (6:144405092 A>T), RS1006886898 (6:144404311 C>A), RS1007376188 (6:144405201 T>A), RS1007818063 (6:144403754 G>A), RS1009948546 (6:144405185 A>G,T), RS1010001163 (6:144405443 G>A,T), RS1010210863 (6:144405081 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.