Hs01472806_cn

• Gene Symbol: C2CD2
• Assay Reference Genome Location: Chr.21:41885755 on build GRCh38
• Cytoband: 21q22.3

Target Gene Details

• Entrez Gene ID: 25966
• Gene Name: C2 calcium dependent domain containing 2
• Gene Aliases: C21orf25, C21orf258, TMEM24L
• Location: Chr.21:41885110-41953957 on Build GRCh38
• Assay Gene Location: Within Exon 17

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C2CD2	NM_015500.1	14	5702	NP_056315.1
	NM_199050.2	13	5201	NP_950251.1
	XM_011529522.1	14	5802	XP_011527824.1
	XM_017028315.1	11	4938	XP_016883804.1
	AB047784.1	14	5702	BAD74068.1
	AK125120.1	5	4271
	AL050173.1	3	3916	CAB43307.1
	CR627455.1	6	5476	CAH10536.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv587574	Chr.21:41877778 - 41893574 on Build GRCh38	Loss	PRDM15 C2CD2
dgv7851n54	Chr.21:41870944 - 41897914 on Build GRCh38	Loss	PRDM15 C2CD2
nsv587564	Chr.21:41833660 - 41887220 on Build GRCh38	Loss	PRDM15 C2CD2
nsv587565	Chr.21:41863326 - 41888378 on Build GRCh38	Loss	PRDM15 C2CD2

More Information

Additional Information:

For this assay, SNP(s) [rs118060196] 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