Hs04034025_cn

• Gene Symbol: CACNG7
• Assay Reference Genome Location: Chr.19:53929360 on build GRCh38
• Cytoband: 19q13.42

Target Gene Details

• Entrez Gene ID: 59284
• Gene Name: calcium voltage-gated channel auxiliary subunit gamma 7
• Gene Aliases: -
• Location: Chr.19:53909425-53943944 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CACNG7	NM_031896.4			NP_114102.2
	XM_005259124.3			XP_005259181.1
	XM_017027093.1			XP_016882582.1
	AF288387.1			AAK20030.1
	AF361353.1			AAL50048.1
	AF458897.1			AAM00594.1
	BC069332.1			AAH69332.1
	BC093869.1			AAH93869.1
	BC113503.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1064558	Chr.19:53773468 - 53957491 on Build GRCh38	Gain	MIR371A MIR371B NLRP12 LOC105372457 MYADM MIR372 MIR373 PRKCG CACNG7
nsv2541	Chr.19:53901764 - 53946589 on Build GRCh38	Deletion	PRKCG CACNG7
nsv1063127	Chr.19:53926876 - 54068977 on Build GRCh38	Gain	MIR935 CACNG6 VSTM1 CACNG8 CACNG7
esv2718812	Chr.19:53184636 - 54322450 on Build GRCh38	Deletion	MIR525 CNOT3 ZNF765 MIR516A1 MIR518C MIR519E DPRX MIR515-1 ZNF845 ZNF761 LENG1 ZNF818P MIR519A2 ZNF331 MIR520D LILRB3 ZNF525 MIR526A2 MBOAT7 MIR935 MIR521-1 MIR520G TPM3P9 LOC284379 LOC105372457 MIR516A2 MIR515-2 ZNF813 MYADM MIR372 MIR373 TSEN34 PRKCG TFPT NLRP12 MIR523 MIR518A2 MIR516B1 MIR1323 MIR520B MIR520A MIR524 LILRB5 MIR512-1 MIR371A CACNG6 MIR1283-1 MIR520F MIR512-2 MIR517C BIRC8 RPS9 MIR522 MIR526A1 MIR518A1 CACNG7 MIR516B2 ZNF665 NDUFA3 MIR1283-2 MIR527 MIR521-2 TARM1 VSTM1 PRPF31 ZNF677 MIR518B LILRB2 MIR526B TMC4 MIR519D MIR518F OSCAR MIR520H MIR518E MIR498 VN1R2 MIR371B MIR519A1 MIR517B MIR520E LILRA6 MIR4752 LILRA5 MIR520C MIR519B MIR519C VN1R4 MIR518D MIR517A CACNG8 FAM90A27P
nsv833876	Chr.19:53845956 - 53995117 on Build GRCh38	Loss	MIR935 CACNG6 LOC105372457 MYADM PRKCG CACNG8 CACNG7

More Information

Additional Information:

For this assay, SNP(s) [rs78724150] 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, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

voltage-gated ion channel

Gene Ontology Categories:

Process(es)

calcium ion transport
transmission of nerve impulse
cardiac conduction
calcium ion transmembrane transport
regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor activity

Function(s)

voltage-gated calcium channel activity
channel regulator activity