SNAR-A8

Summary

SNAR-A8 (small NF90 (ILF3) associated RNA A8, HGNC:34311) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100169958 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34311
Approved symbol	SNAR-A8
Name	small NF90 (ILF3) associated RNA A8
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	snaR-A55307557
Entrez	100169958
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 121 via entrez): RS1162569283 (19:50114253 C>G), RS1188317385 (19:50114307 T>G), RS1228054720 (19:50114178 T>C), RS1289212025 (19:50114277 T>C), RS1323821825 (19:50112281 G>A), RS1325555218 (19:50114119 C>T), RS1334037133 (19:50114151 A>G), RS1339042580 (19:50112248 T>A,C), RS1339384023 (19:50114144 T>C), RS1385659466 (19:50114234 G>A), RS1412524092 (19:50112251 C>A), RS1456237053 (19:50114262 G>T), RS1475659197 (19:50114319 T>C), RS1555740877 (19:50112452 G>C), RS1568427832 (19:50111965 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.