Hs02899565_cn

• Gene Symbol: C2CD2
• Assay Reference Genome Location: Chr.21:41887205 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	4252	NP_056315.1
	NM_199050.2	13	3751	NP_950251.1
	XM_005261109.4	13	3792	XP_005261166.1
	XM_011529522.1	14	4352	XP_011527824.1
	XM_011529523.2	15	5018	XP_011527825.1
	XM_017028315.1	11	3488	XP_016883804.1
	AB047784.1	14	4252	BAD74068.1
	AK125120.1	5	2821
	AK128550.1	11	3591
	AL050173.1	3	2466	CAB43307.1
	AL833323.1	13	3751
	CR627455.1	6	4026	CAH10536.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv459271	Chr.21:41887220 - 41907962 on Build GRCh38	Loss	C2CD2
nsv828881	Chr.21:41887014 - 41887850 on Build GRCh38	Gain	C2CD2
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

• Set Membership: Intragenic, Exonic, DGV Variation