SNORD164

Summary

SNORD164 (small nucleolar RNA, C/D box 164, HGNC:51878) is a gene on chromosome 11p13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51878
Approved symbol	SNORD164
Name	small nucleolar RNA, C/D box 164
Location	11p13
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623487
RNAcentral	URS0000ABD7FE — snoRNA, 61 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): RS1002328339 (11:35162925 C>A,T), RS1002569274 (11:35162860 T>C), RS1003976502 (11:35162146 A>G), RS1005647814 (11:35160957 A>G), RS1005703629 (11:35161329 T>A,C), RS1006897006 (11:35161930 C>A), RS1007515571 (11:35162158 G>A), RS1008571789 (11:35163339 T>C), RS1011203690 (11:35160968 C>A), RS1011931823 (11:35161589 T>C), RS1015216189 (11:35161643 T>C), RS1015372229 (11:35162410 G>A,C,T), RS1015486874 (11:35162179 C>G,T), RS1016470296 (11:35162926 G>A,T), RS1017050105 (11:35161332 A>G)

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.