SNORA105C

Summary

SNORA105C (small nucleolar RNA, H/ACA box 105C, HGNC:51399) is a gene on chromosome 12q13.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51399
Approved symbol	SNORA105C
Name	small nucleolar RNA, H/ACA box 105C
Location	12q13.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635541
RNAcentral	URS00008E39AC — snoRNA, 116 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): RS1001457662 (12:56512034 G>A,T), RS1001508547 (12:56512470 G>A), RS1002099166 (12:56511743 G>A,T), RS1002948552 (12:56510920 C>T), RS1005446967 (12:56512518 G>A), RS1006568297 (12:56513253 G>A), RS1006686018 (12:56513024 T>C), RS1006695759 (12:56513346 T>A,G), RS1009918648 (12:56513470 A>G), RS1012213016 (12:56513213 G>C,T), RS1014676738 (12:56511556 T>C), RS1015922202 (12:56512548 T>G), RS1019323564 (12:56513257 G>A), RS1025311913 (12:56511146 G>A,C), RS1028462142 (12:56510997 C>G,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.