SNAR-A2

Summary

SNAR-A2 (small NF90 (ILF3) associated RNA A2, HGNC:34305) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100126799 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34305
Approved symbol	SNAR-A2
Name	small NF90 (ILF3) associated RNA A2
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	SNAR-A53129250
Entrez	100126799
RNAcentral	URS00003848F7 — ncRNA, 122 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 236 via entrez): RS1045669925 (19:47934283 G>A), RS112554108 (19:47934434 C>A), RS112730971 (19:47933883 C>T), RS112750155 (19:47934294 C>T), RS1157093315 (19:47934235 C>CG), RS1157403262 (19:47934595 C>A), RS1165269396 (19:47934327 C>A), RS1167973249 (19:47934445 G>A), RS1172445264 (19:47934440 C>T), RS1177637036 (19:47934260 G>A), RS1191044252 (19:47934397 CTTT>C,CT,CTT,CTTTT,CTTTTT), RS1191131813 (19:47934234 G>A,T), RS1192543087 (19:47934486 G>A), RS1193632270 (19:47934510 C>G), RS1206126435 (19:47934661 C>T)

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.