SNAR-A14

Summary

SNAR-A14 (small NF90 (ILF3) associated RNA A14, HGNC:34338) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100191063 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34338
Approved symbol	SNAR-A14
Name	small NF90 (ILF3) associated RNA A14
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Aliases	SNAR-A55293015
Entrez	100191063
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): RS111599887 (19:50097833 A>T), RS111739380 (19:50098825 G>A), RS1156591080 (19:50098824 G>C,T), RS1159850365 (19:50099347 C>G), RS1160446967 (19:50098920 C>T), RS1161954053 (19:50098804 C>T), RS1162095743 (19:50099589 C>G), RS1163825315 (19:50099438 G>T), RS1163910248 (19:50099010 G>A,C,T), RS1166336688 (19:50097746 T>C), RS1166733035 (19:50099634 C>T), RS1170744921 (19:50098636 C>T), RS1170798080 (19:50097742 G>A), RS1171134587 (19:50099849 T>C), RS1174175169 (19:50099786 G>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)

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
Benzo(a)pyrene	increases methylation	1

Clinical trials (associated diseases)

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