SNORD173

Summary

SNORD173 (small nucleolar RNA, C/D box 173, HGNC:51887) is a gene on chromosome 8q22.3.

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

Source: NCBI Gene 109623480 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51887
Approved symbol	SNORD173
Name	small nucleolar RNA, C/D box 173
Location	8q22.3
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623480
RNAcentral	URS0000ABD8B0 — snoRNA, 104 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): RS1001098870 (8:103307082 C>T), RS1003294018 (8:103307474 T>A), RS1006678464 (8:103308846 G>A), RS1007198284 (8:103307049 G>A), RS1008871155 (8:103308610 C>G), RS1008922070 (8:103308277 T>A,C), RS1010806009 (8:103307171 T>C), RS1011003375 (8:103307423 G>A), RS1011995556 (8:103308167 C>T), RS1012047908 (8:103307819 G>C), RS1012251526 (8:103307546 CA>C), RS1015051147 (8:103308136 T>C), RS1017273713 (8:103307060 C>G), RS1019170481 (8:103308279 T>G), RS1022573155 (8:103308642 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.