SNAR-A10

Summary

SNAR-A10 (small NF90 (ILF3) associated RNA A10, HGNC:34313) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170216 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34313
Approved symbol	SNAR-A10
Name	small NF90 (ILF3) associated RNA A10
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55318263
Entrez	100170216
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): RS111428952 (19:50122575 G>C), RS112975391 (19:50123056 C>G,T), RS1157048241 (19:50124280 C>A,T), RS1157567294 (19:50123821 G>A), RS1159264473 (19:50123897 A>C,T), RS1161585944 (19:50123343 T>A,G), RS1162542959 (19:50123972 C>G), RS1165711561 (19:50123576 T>A,C), RS1168104789 (19:50123987 T>G), RS1171393656 (19:50123671 C>A,T), RS1172766042 (19:50124085 G>A,T), RS1173460077 (19:50123550 T>C), RS1175990368 (19:50123890 CA>C), RS1176344215 (19:50123693 T>C), RS1177957752 (19:50123978 AAACGTTTTTGC>A)

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.