SNAR-G2

Summary

SNAR-G2 (small NF90 (ILF3) associated RNA G2, HGNC:34328) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170228 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34328
Approved symbol	SNAR-G2
Name	small NF90 (ILF3) associated RNA G2
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Entrez	100170228
RNAcentral	URS00004E5347 — ncRNA, 119 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): RS1000447906 (19:49031911 C>A), RS1001724214 (19:49031721 C>G,T), RS1003520882 (19:49032911 G>A,C,T), RS1005514294 (19:49031733 C>G,T), RS1005852474 (19:49031172 C>A,G,T), RS1005905010 (19:49031332 C>G), RS1006801131 (19:49033659 G>A), RS1008419223 (19:49032255 A>C,G,T), RS1008476090 (19:49032371 G>A,C), RS1010371713 (19:49031579 A>G), RS1010466592 (19:49031686 A>C,G,T), RS1011052792 (19:49033722 A>G), RS1012320165 (19:49032401 G>A,C), RS1012709065 (19:49031916 A>C), RS1012779283 (19:49032843 G>T)

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

8 total (human), top 8 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Benzo(a)pyrene	affects methylation	1
Glycerol	affects cotreatment, increases expression	1
Nicotine	increases expression, affects cotreatment	1
Rotenone	decreases expression	1
Silicon Dioxide	decreases expression	1
Tobacco Smoke Pollution	increases expression	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.