SNAR-A12

Summary

SNAR-A12 (small NF90 (ILF3) associated RNA A12, HGNC:34315) is a gene on chromosome 19q13.33.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100126800 — RefSeq curated summary.

At a glance

• GWAS associations: 1

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34315
Approved symbol	SNAR-A12
Name	small NF90 (ILF3) associated RNA A12
Location	19q13.33
Locus type	RNA, misc
Status	Approved
Entrez	100126800
RNAcentral	URS000010A63C — 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 300 via entrez): RS1012935129 (19:47907639 C>A), RS1045723767 (19:47907780 G>A), RS1157082403 (19:47906879 A>C), RS1157207644 (19:47906990 T>A,C,G), RS1157264158 (19:47907791 C>CT,CTT), RS1157283430 (19:47907030 G>A,T), RS1160675144 (19:47907700 A>C,G,T), RS1160920973 (19:47907514 A>C,G), RS1163347309 (19:47907737 G>A,T), RS1164399503 (19:47906965 A>T), RS1167007544 (19:47907044 A>G), RS1167876603 (19:47907267 G>A,T), RS1170604546 (19:47907488 C>A,G), RS1170659904 (19:47907433 C>G), RS1172571041 (19:47906987 T>C)

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

1 associations (top):

Study	Trait	p-value
GCST012020_543	Serum metabolite levels	6.000000e-35

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.