SNAR-A4

Summary

SNAR-A4 (small NF90 (ILF3) associated RNA A4, HGNC:34307) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100169956 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34307
Approved symbol	SNAR-A4
Name	small NF90 (ILF3) associated RNA A4
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55287678
Entrez	100169956
RNAcentral	URS00004E56CF — ncRNA, 121 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): RS1011667195 (19:50093897 T>A), RS1023430074 (19:50094535 G>A,T), RS1031650552 (19:50093149 T>G), RS113353798 (19:50093278 C>A,G,T), RS113579783 (19:50093279 A>G,T), RS1156305817 (19:50093316 G>C), RS1156993802 (19:50094338 C>A,G), RS1157678708 (19:50093091 T>C), RS1159317504 (19:50093272 C>G), RS1159873190 (19:50094184 A>G,T), RS1159915360 (19:50092107 A>G), RS1162864166 (19:50092226 A>T), RS1163948252 (19:50094210 G>A,T), RS1164268698 (19:50094445 T>G), RS1164270013 (19:50092321 G>A,C)

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)

Clinical trials (associated diseases)

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