SNAR-C2

Summary

SNAR-C2 (small NF90 (ILF3) associated RNA C2, HGNC:34320) is a gene on chromosome 19q13.32.

Predicted to be located in cytoplasm and nucleus.

Source: NCBI Gene 100170218 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:34320
Approved symbol	SNAR-C2
Name	small NF90 (ILF3) associated RNA C2
Location	19q13.32
Locus type	RNA, misc
Status	Approved
Entrez	100170218
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): RS113911137 (19:47928128 T>G), RS1157040319 (19:47928858 G>A,T), RS1157361991 (19:47928793 A>G,T), RS1157543005 (19:47927595 G>A), RS1159103366 (19:47928761 G>A), RS1159200887 (19:47928786 A>C,G,T), RS1159254425 (19:47927045 AC>A), RS1159315550 (19:47927251 T>A,C), RS1159368777 (19:47929431 C>T), RS1160373968 (19:47928170 C>A,T), RS1161953218 (19:47928851 G>A), RS1162438756 (19:47928351 C>G), RS1164048481 (19:47927014 G>A,C), RS1164206799 (19:47928330 G>A,T), RS1164555141 (19:47928791 A>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

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.