SNAR-A6

Summary

SNAR-A6 (small NF90 (ILF3) associated RNA A6, HGNC:34309) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100169957 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34309
Approved symbol	SNAR-A6
Name	small NF90 (ILF3) associated RNA A6
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55299144
Entrez	100169957
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): RS111856365 (19:50104720 C>A,G,T), RS112325040 (19:50105537 A>C,G), RS112926278 (19:50104953 G>A), RS1156312350 (19:50106004 C>A,T), RS1156857358 (19:50104703 C>A,T), RS1161166800 (19:50103699 A>G), RS1161638555 (19:50104855 TTCTG>T), RS1166127227 (19:50105087 C>G), RS1166855530 (19:50103967 T>C), RS1167635433 (19:50105899 G>A,C), RS1170804552 (19:50104195 G>GCC), RS1172388737 (19:50106071 C>G), RS1173008735 (19:50104672 G>A), RS1174633392 (19:50105950 C>T), RS1175577672 (19:50104842 T>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)

Clinical trials (associated diseases)

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