Hs01403674_cn

• Gene Symbol: TC2N
• Assay Reference Genome Location: Chr.14:91782447 on build GRCh38
• Cytoband: 14q32.12

Target Gene Details

• Entrez Gene ID: 123036
• Gene Name: tandem C2 domains, nuclear
• Gene Aliases: C14orf47, C2CD1, MTAC2D1, Tac2-N
• Location: Chr.14:91779751-91867536 on Build GRCh38
• Assay Gene Location: Within Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TC2N	NM_001128595.2	12	2338	NP_001122067.1
	NM_001128596.2	12	2457	NP_001122068.1
	NM_001289134.1	11	2146	NP_001276063.1
	NM_152332.5	12	2526	NP_689545.1
	BC040503.1	12	2339	AAH40503.1
	BX647828.1	12	2260
	BX648227.1	2	252

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv3635327	Chr.14:91717848 - 91867474 on Build GRCh38	Gain	TC2N CATSPERB
nsv1053264	Chr.14:91781715 - 91827174 on Build GRCh38	Loss	TC2N

More Information

Additional Information:

For this assay, SNP(s) [rs114965754] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

vesicle fusion
regulation of gene expression
regulation of calcium ion-dependent exocytosis
regulation of blood coagulation
calcium ion-regulated exocytosis of neurotransmitter

Function(s)

molecular_function
calcium ion binding
calcium-dependent phospholipid binding
syntaxin binding
clathrin binding