SNAR-C4

Summary

SNAR-C4 (small NF90 (ILF3) associated RNA C4, HGNC:34322) is a gene on chromosome 19q13.32.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170219 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34322
Approved symbol	SNAR-C4
Name	small NF90 (ILF3) associated RNA C4
Location	19q13.32
Locus type	RNA, misc
Status	Approved
Entrez	100170219
RNAcentral	URS0000268556 — ncRNA, 120 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): RS1157292177 (19:47937617 T>C), RS1157939653 (19:47938134 C>A,G,T), RS1160015179 (19:47938661 C>T), RS1160706754 (19:47939668 C>G,T), RS1161219764 (19:47938844 G>T), RS1161771404 (19:47939589 G>GT), RS1161976869 (19:47939897 G>T), RS1163512253 (19:47938859 T>G), RS1164946482 (19:47939763 T>C), RS1165179994 (19:47938854 T>G), RS1166951529 (19:47939168 G>A), RS1167236733 (19:47939568 G>GCGCGGGCC), RS1167341901 (19:47939651 A>C,G,T), RS1167776880 (19:47939610 A>G), RS1169641935 (19:47938124 T>TC)

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

2 total (human), top 2 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
2-methyl-4-isothiazolin-3-one	increases expression	1
didecyldimethylammonium	decreases expression	1

Clinical trials (associated diseases)

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