SNORA95

Summary

SNORA95 (small nucleolar RNA, H/ACA box 95, HGNC:50399) is a gene on chromosome 3p12.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50399
Approved symbol	SNORA95
Name	small nucleolar RNA, H/ACA box 95
Location	3p12.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635529
RNAcentral	URS00008E39CA — snoRNA, 112 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): RS1001707251 (3:85061802 TAC>T), RS1003567577 (3:85062462 C>T), RS1005302298 (3:85063385 A>T), RS1006275442 (3:85063855 GT>G), RS1006634925 (3:85064084 T>C), RS1006782087 (3:85063584 GAA>G), RS1007750435 (3:85062353 A>G), RS1008573865 (3:85062030 T>C), RS1008954454 (3:85061864 C>T), RS1009811535 (3:85062761 A>C), RS1010073614 (3:85062396 G>A,T), RS1012160567 (3:85063811 G>A,C), RS1012280368 (3:85063118 A>G), RS1012540614 (3:85064257 G>A), RS1014951286 (3:85062024 T>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.