SNAR-A5

Summary

SNAR-A5 (small NF90 (ILF3) associated RNA A5, HGNC:34308) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100169952 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34308
Approved symbol	SNAR-A5
Name	small NF90 (ILF3) associated RNA A5
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55296080
Entrez	100169952
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): RS1049496880 (19:50101658 G>A), RS113046716 (19:50101011 G>A), RS1160397684 (19:50100412 G>A,T), RS1162393981 (19:50103008 C>G,T), RS1166017422 (19:50100436 G>T), RS1171124841 (19:50102996 C>A,T), RS1171993092 (19:50101726 C>A,G,T), RS1176530181 (19:50100396 G>A,C,T), RS1179044200 (19:50102934 G>A,C), RS1182403190 (19:50102945 T>A,G), RS1183960711 (19:50101611 T>G), RS1193267958 (19:50102982 T>C,G), RS1193572327 (19:50102039 G>C), RS1196531499 (19:50100620 C>A,T), RS1197326043 (19:50102959 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)

Clinical trials (associated diseases)

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