SNAR-F

Summary

SNAR-F (small NF90 (ILF3) associated RNA F, HGNC:34326) is a gene on chromosome 19q13.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34326
Approved symbol	SNAR-F
Name	small NF90 (ILF3) associated RNA F
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Entrez	100126781
RNAcentral	URS000028A228 — ncRNA, 123 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): RS1003700246 (19:50603120 C>A), RS1012054292 (19:50603425 C>T), RS1014645567 (19:50604625 A>G), RS1015337310 (19:50603197 T>C), RS1015431136 (19:50604495 A>C), RS1015503461 (19:50603601 C>A,T), RS1024320717 (19:50604815 TAC>T), RS1027546950 (19:50603180 C>A,T), RS1028053365 (19:50604292 A>G), RS1028158252 (19:50603262 T>TC), RS1032028334 (19:50603236 CTCTT>C), RS1032059479 (19:50602987 A>G), RS1034808912 (19:50603124 C>G), RS1040736007 (19:50603835 G>A,T), RS10421679 (19:50604187 C>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: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

9 total (human), top 9 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Benzo(a)pyrene	affects methylation	1
Glycerol	increases expression, affects cotreatment	1
Nicotine	affects cotreatment, increases expression	1
Rotenone	decreases expression	1
Silicon Dioxide	decreases expression	1
Tobacco Smoke Pollution	increases expression	1
Valproic Acid	increases methylation	1
Cadmium Chloride	decreases expression	1
Propylene Glycol	affects cotreatment, increases expression	1

Clinical trials (associated diseases)

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