SNAR-C1

Summary

SNAR-C1 (small NF90 (ILF3) associated RNA C1, HGNC:34319) is a gene on chromosome 19q13.32.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170225 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34319
Approved symbol	SNAR-C1
Name	small NF90 (ILF3) associated RNA C1
Location	19q13.32
Locus type	RNA, misc
Status	Approved
Entrez	100170225
RNAcentral	URS0000405895 — ncRNA, 120 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): RS1008466284 (19:47955530 C>G), RS1019820299 (19:47955533 A>C), RS111394127 (19:47953834 C>A,T), RS111963791 (19:47954975 G>A,C,T), RS112385489 (19:47955467 T>C), RS113460119 (19:47956018 C>A), RS113522468 (19:47955228 G>C,T), RS113778070 (19:47954262 G>C), RS1156720976 (19:47955925 C>G,T), RS1156723784 (19:47954504 C>A,G), RS1158938105 (19:47955209 G>C,T), RS1159822231 (19:47955573 G>A), RS1160421046 (19:47953829 G>T), RS1160456026 (19:47955248 G>A,C,T), RS1162007285 (19:47955917 T>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.