SNORD172

Summary

SNORD172 (small nucleolar RNA, C/D box 172, HGNC:51886) is a gene on chromosome 10q22.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51886
Approved symbol	SNORD172
Name	small nucleolar RNA, C/D box 172
Location	10q22.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623471
RNAcentral	URS0000ABD8A3 — snoRNA, 59 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): RS1000247249 (10:75019972 T>C), RS1000711605 (10:75022138 GGAA>G), RS1000941937 (10:75020431 A>G), RS1001365993 (10:75020415 C>G,T), RS1003088192 (10:75022251 T>G), RS1004723366 (10:75021422 C>T), RS1004976602 (10:75021433 T>C), RS1008777431 (10:75021781 T>C,G), RS1009262971 (10:75022024 A>C), RS1009784242 (10:75020404 C>A,T), RS1013657223 (10:75021155 T>C), RS1014240172 (10:75020394 G>A), RS1014686444 (10:75020074 A>G), RS1015206398 (10:75020954 A>C,G), RS1016502364 (10:75021435 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.