SNORA107

Summary

SNORA107 (small nucleolar RNA, H/ACA box 107, HGNC:51400) is a gene on chromosome 13q31.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51400
Approved symbol	SNORA107
Name	small nucleolar RNA, H/ACA box 107
Location	13q31.1
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635542
RNAcentral	URS00008E3A02 — snoRNA, 125 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): RS1000104510 (13:84782770 G>A), RS1001634652 (13:84784117 A>G), RS1002133334 (13:84781686 G>A), RS1003232905 (13:84783067 T>A), RS1005396537 (13:84782233 AT>A), RS1005509322 (13:84782010 G>T), RS1005691473 (13:84782143 C>T), RS1006056376 (13:84783134 A>G,T), RS1006133645 (13:84781855 C>T), RS1007067123 (13:84783453 G>A), RS1007183382 (13:84783196 T>G), RS1008343135 (13:84784036 G>T), RS1008623897 (13:84783716 A>G), RS1008854998 (13:84784276 C>A,T), RS1009580836 (13:84781948 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.