SNORD175

Summary

SNORD175 (small nucleolar RNA, C/D box 175, HGNC:51889) is a gene on chromosome 19q13.2.

Predicted to be involved in RNA processing. Predicted to be located in nucleolus.

Source: NCBI Gene 109623469 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51889
Approved symbol	SNORD175
Name	small nucleolar RNA, C/D box 175
Location	19q13.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623469
RNAcentral	URS0000ABD7D4 — snoRNA, 72 nt, 3 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): RS1001918835 (19:39467680 C>A,G,T), RS1001973154 (19:39466924 TAA>T), RS1004366702 (19:39467623 C>T), RS1008492041 (19:39467027 T>C), RS1009292422 (19:39466703 T>G), RS1010229241 (19:39467000 A>C), RS1010699162 (19:39468000 G>A), RS1018840203 (19:39468422 C>G,T), RS1019201896 (19:39468132 C>T), RS1019476898 (19:39467354 G>T), RS1020470991 (19:39468008 T>C), RS1020471505 (19:39466613 G>A,C), RS1020808448 (19:39467761 T>C), RS1020860845 (19:39468104 C>T), RS1024707818 (19:39467378 G>A,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.