Hs03397419_cn

• Gene Symbol: POTEI
• Assay Reference Genome Location: Chr.2:130726552 on build GRCh38
• Cytoband: 2q21.1

Target Gene Details

• Entrez Gene ID: 653269
• Gene Name: POTE ankyrin domain family member I
• Gene Aliases: POTE2beta
• Location: Chr.2:130462245-131626428 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
POTEI

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv4074n100	Chr.2:130550793 - 131291209 on Build GRCh38	Gain	POTEE TISP43 AMER3 POTEJ CFC1 GPR148 ARHGEF4 LOC440910 PLEKHB2 FAM168B CYP4F30P POTEI
dgv731e199	Chr.2:130678437 - 131300107 on Build GRCh38	Deletion	POTEE AMER3 GPR148 ARHGEF4 LOC440910 PLEKHB2 FAM168B CYP4F30P POTEI
esv2670824	Chr.2:130625264 - 131605218 on Build GRCh38	Deletion	WTH3DI MZT2A AMER3 GPR148 ARHGEF4 LOC440910 FAM168B POTEKP POTEE POTEJ LOC150776 LINC01120 CCDC74A TUBA3D MIR4784 PLEKHB2 NOC2LP2 CYP4F30P POTEI
esv3893337	Chr.2:130722838 - 131194387 on Build GRCh38	Loss	AMER3 GPR148 ARHGEF4 PLEKHB2 FAM168B POTEI
dgv616e201	Chr.2:130674635 - 131312550 on Build GRCh38	Deletion	POTEE AMER3 GPR148 ARHGEF4 LOC440910 PLEKHB2 FAM168B CYP4F30P POTEI
esv3575299	Chr.2:130680940 - 130753107 on Build GRCh38	Gain	GPR148 CYP4F30P POTEI
nsv1014723	Chr.2:130720375 - 131379551 on Build GRCh38	Loss	POTEE WTH3DI AMER3 GPR148 ARHGEF4 LOC440910 PLEKHB2 FAM168B POTEI
nsv583135	Chr.2:130724905 - 131194388 on Build GRCh38	Loss	AMER3 GPR148 ARHGEF4 PLEKHB2 FAM168B POTEI
nsv524021	Chr.2:130724906 - 131553515 on Build GRCh38	Loss	WTH3DI MZT2A AMER3 GPR148 ARHGEF4 LOC440910 FAM168B POTEE LOC150776 LINC01120 CCDC74A TUBA3D MIR4784 PLEKHB2 NOC2LP2 POTEI
esv2760576	Chr.2:130634172 - 131521752 on Build GRCh38	Gain+Loss	WTH3DI MZT2A AMER3 GPR148 ARHGEF4 LOC440910 FAM168B POTEE POTEJ LOC150776 LINC01120 TUBA3D MIR4784 PLEKHB2 NOC2LP2 CYP4F30P POTEI
esv2759092	Chr.2:129589265 - 132440430 on Build GRCh38	Gain+Loss	RAB6C AMER3 ANKRD30BL LINC01087 FAM168B TISP43 LINC01120 C2orf27B TUBA3D MED15P9 CYP4F30P MZT2A CFC1 ARHGEF4 LOC440910 C2orf27A CFC1B IMP4 MIR4784 MZT2B NOC2LP2 WTH3DI FAM201B GPR148 FAR2P2 RAB6C-AS1 SMPD4 POTEE POTEJ LOC150776 NOC2LP1 LOC646743 CCDC74A TUBA3E POTEF FAR2P1 CCDC74B CCDC115 POTEI CYP4F62P GPR39 ZNF806 LOC389033 MIR663B POTEKP LOC100507460 LOC101927924 PTPN18 PLEKHB2 LOC107985778
nsv428403	Chr.2:129818076 - 130882067 on Build GRCh38	Loss	RAB6C AMER3 GPR148 FAR2P2 RAB6C-AS1 SMPD4 TISP43 POTEJ NOC2LP1 LOC646743 MED15P9 TUBA3E POTEF FAR2P1 CYP4F30P CCDC74B CCDC115 POTEI CYP4F62P CFC1 ARHGEF4 LOC389033 CFC1B IMP4 LOC101927924 PTPN18 MZT2B LOC107985778

More Information

Additional Information:

For this assay, SNP(s) [rs77516077] 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