Hs04781970_cn

• Gene Symbol: CCDC14
• Assay Reference Genome Location: Chr.3:123897247 on build GRCh38
• Cytoband: 3q21.1

Target Gene Details

• Entrez Gene ID: 64770
• Gene Name: coiled-coil domain containing 14
• Gene Aliases: -
• Location: Chr.3:123887383-123961412 on Build GRCh38
• Assay Gene Location: Overlaps Intron 13 - Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC14	XM_005247715.4			XP_005247772.1
	XM_011513081.2			XP_011511383.1
	XM_017007061.1			XP_016862550.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3597633	Chr.3:123813223 - 123952334 on Build GRCh38	Gain	MYLK CCDC14
nsv591428	Chr.3:123608828 - 124139902 on Build GRCh38	Gain	MYLK-AS1 ROPN1 MYLK MIR5002 CCDC14 MYLK-AS2 KALRN
nsv3979	Chr.3:123854567 - 123898685 on Build GRCh38	Insertion	MYLK CCDC14
nsv1007525	Chr.3:123876493 - 123958230 on Build GRCh38	Loss	MYLK CCDC14

More Information

Additional Information:

For this assay, SNP(s) [rs115528102] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

substantia nigra development
protein localization to centrosome

Function(s)

protein binding