SNAR-A7

Summary

SNAR-A7 (small NF90 (ILF3) associated RNA A7, HGNC:34310) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100169953 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34310
Approved symbol	SNAR-A7
Name	small NF90 (ILF3) associated RNA A7
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55302203
Entrez	100169953
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): RS1161613169 (19:50106533 G>C,T), RS1164126713 (19:50106605 G>C,T), RS1169897990 (19:50108434 G>T), RS1170322884 (19:50106609 A>C,G), RS1175485950 (19:50106522 T>A,C), RS1182788159 (19:50106555 AG>A), RS1184693639 (19:50106594 A>C,G), RS1188482030 (19:50106653 C>T), RS1193335544 (19:50106674 C>G), RS1202548620 (19:50106588 C>G), RS1207308710 (19:50106642 G>C,T), RS1212772310 (19:50106637 T>C), RS1216498625 (19:50106897 C>A), RS1223715359 (19:50106844 G>A,C,T), RS1228671274 (19:50106559 C>A,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.