SNORD167

Summary

SNORD167 (small nucleolar RNA, C/D box 167, HGNC:51881) is a gene on chromosome 1p36.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51881
Approved symbol	SNORD167
Name	small nucleolar RNA, C/D box 167
Location	1p36.33
Locus type	RNA, small nucleolar
Status	Approved
Entrez	109623456
RNAcentral	URS0000ABD8DD — snoRNA, 84 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): RS1000249074 (1:1305384 G>A,C,T), RS1004845635 (1:1306711 C>T), RS1005670410 (1:1305894 C>G), RS1005682899 (1:1304365 TGCCCTCGGGGAAGAAG>T), RS1005802160 (1:1305726 G>GC), RS1006134465 (1:1304857 CG>C), RS1006930480 (1:1304994 G>C), RS1007228873 (1:1305155 C>A,T), RS1009251360 (1:1304359 C>T), RS1009590578 (1:1304274 G>A,T), RS1011447994 (1:1306469 G>A,T), RS1011828681 (1:1305662 T>G), RS1011943443 (1:1305466 C>T), RS1013009234 (1:1305799 C>A,T), RS1013538975 (1:1305592 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

CTD chemical–gene interactions

3 total (human), top 3 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
benzo(e)pyrene	decreases methylation	1
Methapyrilene	decreases methylation	1
Smoke	decreases expression	1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.