SNORA115

Summary

SNORA115 (small nucleolar RNA, H/ACA box 115, HGNC:51853) is a gene on chromosome 2q35.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51853
Approved symbol	SNORA115
Name	small nucleolar RNA, H/ACA box 115
Location	2q35
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623482
RNAcentral	URS0000ABD8C8 — snoRNA, 144 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): RS1000552857 (2:217834783 G>A), RS1002353297 (2:217833196 G>A,T), RS1003621021 (2:217834352 T>C), RS1003975021 (2:217834755 G>A), RS1005910193 (2:217835501 C>T), RS1006905569 (2:217834208 C>A,T), RS1008484085 (2:217835069 G>A), RS1008889083 (2:217835378 T>C), RS1010620386 (2:217833456 C>T), RS1012283553 (2:217834985 G>A,C), RS1012814670 (2:217835058 A>C,G,T), RS1013824133 (2:217833832 C>T), RS1014079385 (2:217835351 C>A,T), RS1015703434 (2:217835319 T>C), RS1016889923 (2:217834012 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.