SNORD163

Summary

SNORD163 (small nucleolar RNA, C/D box 163, HGNC:51877) is a gene on chromosome 17p11.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51877
Approved symbol	SNORD163
Name	small nucleolar RNA, C/D box 163
Location	17p11.2
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623477
RNAcentral	URS0000ABD853 — snoRNA, 64 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): RS1000285842 (17:16152883 C>A,T), RS1000387566 (17:16153085 C>T), RS1005736922 (17:16154013 T>A), RS1005936248 (17:16154323 T>C), RS1006198796 (17:16154504 G>T), RS1007191880 (17:16153696 A>C), RS1008090544 (17:16155122 T>C), RS1008688489 (17:16153727 G>C), RS1011545677 (17:16155164 A>G), RS1011640613 (17:16154777 G>A), RS1013168946 (17:16154031 T>A), RS1013615904 (17:16154367 A>T), RS1014202622 (17:16152861 T>C), RS1017080695 (17:16154024 T>C), RS1017419171 (17:16154518 G>A)

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.