Hs02716084_cn

• Gene Symbol: C1QL3
• Assay Reference Genome Location: Chr.10:16520585 on build GRCh38
• Cytoband: 10p13

Target Gene Details

• Entrez Gene ID: 389941
• Gene Name: complement C1q like 3
• Gene Aliases: C1QTNF13, C1ql, CTRP13, K100
• Location: Chr.10:16513743-16522005 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C1QL3	NM_001010908.1	1	1421	NP_001010908.1
	BC127716.1	2	489
	BC127717.1	2	435

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv25020	Chr.10:16519159 - 16526059 on Build GRCh38	Deletion	C1QL3
nsv831797	Chr.10:16514510 - 16690309 on Build GRCh38	Loss	RSU1 PTER C1QL3
nsv1046833	Chr.10:16385108 - 16530259 on Build GRCh38	Gain	PTER C1QL3

More Information

Additional Information:

For this assay, SNP(s) [rs75810014] 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)

regulation of synapse organization