Hs03925621_cn

• Gene Symbol: KCNG4
• Assay Reference Genome Location: Chr.16:84225582 on build GRCh38
• Cytoband: 16q24.1

Target Gene Details

• Entrez Gene ID: 93107
• Gene Name: potassium voltage-gated channel modifier subfamily G member 4
• Gene Aliases: KV6.3, KV6.4
• Location: Chr.16:84221135-84239750 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
KCNG4	NM_172347.2			NP_758857.1
	AF348984.1			AAL83911.1
	AF450108.1			AAP46289.1
	BC109203.2			AAI09204.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3639413	Chr.16:84172318 - 84253359 on Build GRCh38	Loss	TAF1C ADAD2 KCNG4 DNAAF1
nsv833310	Chr.16:84206440 - 84372385 on Build GRCh38	Loss	KCNG4 WFDC1 ATP2C2 LOC105376777
nsv833309	Chr.16:84076867 - 84248591 on Build GRCh38	Loss	TAF1C LOC729887 ADAD2 HSDL1 KCNG4 DNAAF1 MBTPS1
nsv1065790	Chr.16:83830329 - 84243597 on Build GRCh38	Loss	TAF1C LOC729887 ADAD2 SLC38A8 HSDL1 KCNG4 DNAAF1 MBTPS1 LOC105371371 OSGIN1 MLYCD NECAB2
esv2761930	Chr.16:84007420 - 84312461 on Build GRCh38	Gain	TAF1C LOC729887 ADAD2 SLC38A8 HSDL1 KCNG4 WFDC1 DNAAF1 MBTPS1 LOC105376777
esv3639414	Chr.16:84176251 - 84352273 on Build GRCh38	Loss	TAF1C ADAD2 KCNG4 WFDC1 DNAAF1 LOC105376777
nsv1111143	Chr.16:84219450 - 84226725 on Build GRCh38	Tandem Duplication	KCNG4
nsv483044	Chr.16:84166395 - 87066394 on Build GRCh38	Gain	LINC00311 FOXC2 MIR6774 LOC400548 COX4I1 LINC00917 EMC8 DNAAF1 LOC101928557 LINC01082 GSE1 KIAA0513 TLDC1 FLJ30679 LOC105376777 FENDRR CRISPLD2 C16orf74 FAM92B ZDHHC7 KLHL36 FOXC2-AS1 LOC105371374 IRF8 TAF1C USP10 LOC102724344 MIR5093 FOXF1 MTHFSD ATP2C2 LOC146513 LOC101928474 GINS2 LOC101928614 LINC01081 ADAD2 KCNG4 LOC440390 WFDC1 FOXL1 COTL1 MIR1910
nsv1059227	Chr.16:84029323 - 84233403 on Build GRCh38	Loss	TAF1C LOC729887 ADAD2 SLC38A8 HSDL1 KCNG4 DNAAF1 MBTPS1

More Information

Additional Information:

For this assay, SNP(s) [rs77104975] 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)

regulation of ion transmembrane transport
protein homooligomerization
potassium ion transmembrane transport

Function(s)

delayed rectifier potassium channel activity
ion channel binding