SNAR-G1

Summary

SNAR-G1 (small NF90 (ILF3) associated RNA G1, HGNC:34327) is a gene on chromosome 19q13.33.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34327
Approved symbol	SNAR-G1
Name	small NF90 (ILF3) associated RNA G1
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Entrez	100126780
RNAcentral	URS00005D5557 — ncRNA, 128 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): RS1002736778 (19:49036378 C>T), RS1002813143 (19:49036922 A>C), RS1003198893 (19:49036485 AC>A), RS1004580892 (19:49037598 CCG>C), RS1006251902 (19:49037034 G>A,C,T), RS1006262953 (19:49037077 G>A,C,T), RS1006593052 (19:49036667 C>G), RS1006650939 (19:49036829 C>A,G), RS1008654367 (19:49035407 C>T), RS1009046089 (19:49035210 G>C), RS1010213588 (19:49037356 G>A), RS1010546302 (19:49036983 G>A), RS1012223893 (19:49036468 C>A,T), RS1013183467 (19:49035532 G>A,C), RS1013353412 (19:49037407 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: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

6 total (human), top 6 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
sodium arsenite	increases expression	1
Benzo(a)pyrene	increases methylation	1
Tobacco Smoke Pollution	increases expression	1
Valproic Acid	increases methylation	1
Cadmium Chloride	decreases expression	1
Lactic Acid	increases expression	1

Clinical trials (associated diseases)

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