Hs04678588_cn

• Gene Symbol: POTEI
• Assay Reference Genome Location: Chr.2:130738173 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	POTEI GPR148 POTEJ CFC1 PLEKHB2 AMER3 CYP4F30P POTEE TISP43 LOC440910 FAM168B ARHGEF4
dgv731e199	Chr.2:130678437 - 131300107 on Build GRCh38	Deletion	POTEI GPR148 PLEKHB2 AMER3 CYP4F30P POTEE LOC440910 FAM168B ARHGEF4
esv2670824	Chr.2:130625264 - 131605218 on Build GRCh38	Deletion	POTEI GPR148 POTEJ POTEKP MIR4784 TUBA3D WTH3DI CYP4F30P MZT2A POTEE NOC2LP2 CCDC74A PLEKHB2 AMER3 LINC01120 LOC150776 LOC440910 FAM168B ARHGEF4
nsv583136	Chr.2:130730100 - 130846832 on Build GRCh38	Loss	POTEI GPR148 AMER3 ARHGEF4
dgv4075n100	Chr.2:130720375 - 131521740 on Build GRCh38	Gain	POTEI GPR148 MIR4784 TUBA3D WTH3DI MZT2A POTEE NOC2LP2 PLEKHB2 AMER3 LINC01120 LOC150776 LOC440910 FAM168B ARHGEF4
esv3893337	Chr.2:130722838 - 131194387 on Build GRCh38	Loss	POTEI GPR148 PLEKHB2 AMER3 FAM168B ARHGEF4
esv3575299	Chr.2:130680940 - 130753107 on Build GRCh38	Gain	POTEI GPR148 CYP4F30P
dgv616e201	Chr.2:130674635 - 131312550 on Build GRCh38	Deletion	POTEI GPR148 PLEKHB2 AMER3 CYP4F30P POTEE LOC440910 FAM168B ARHGEF4
nsv583135	Chr.2:130724905 - 131194388 on Build GRCh38	Loss	POTEI GPR148 PLEKHB2 AMER3 FAM168B ARHGEF4
nsv524021	Chr.2:130724906 - 131553515 on Build GRCh38	Loss	POTEI GPR148 MIR4784 TUBA3D WTH3DI MZT2A POTEE NOC2LP2 CCDC74A PLEKHB2 AMER3 LINC01120 LOC150776 LOC440910 FAM168B ARHGEF4
esv2760576	Chr.2:130634172 - 131521752 on Build GRCh38	Gain+Loss	POTEI GPR148 POTEJ MIR4784 TUBA3D WTH3DI CYP4F30P MZT2A POTEE NOC2LP2 PLEKHB2 AMER3 LINC01120 LOC150776 LOC440910 FAM168B ARHGEF4
esv2759092	Chr.2:129589265 - 132440430 on Build GRCh38	Gain+Loss	FAR2P2 LOC100507460 TUBA3D CYP4F30P POTEE TISP43 NOC2LP2 TUBA3E FAR2P1 AMER3 LOC150776 CCDC74B FAM168B LINC01087 LOC101927924 POTEKP LOC389033 FAM201B SMPD4 PLEKHB2 IMP4 CYP4F62P RAB6C ARHGEF4 POTEI GPR148 LOC646743 GPR39 MZT2B MIR4784 MZT2A CCDC115 RAB6C-AS1 NOC2LP1 CCDC74A ANKRD30BL LINC01120 PTPN18 LOC440910 C2orf27A POTEJ CFC1 MIR663B CFC1B WTH3DI C2orf27B ZNF806 POTEF LOC107985778 MED15P9
nsv428403	Chr.2:129818076 - 130882067 on Build GRCh38	Loss	POTEI GPR148 LOC646743 FAR2P2 MZT2B CYP4F30P CCDC115 RAB6C-AS1 TISP43 NOC2LP1 TUBA3E FAR2P1 AMER3 CCDC74B PTPN18 LOC101927924 POTEJ CFC1 CFC1B LOC389033 SMPD4 POTEF IMP4 LOC107985778 CYP4F62P RAB6C MED15P9 ARHGEF4

More Information

Additional Information:

For this assay, SNP(s) [rs75557753] 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