Hs04572142_cn

• Gene Symbol: POTEI
• Assay Reference Genome Location: Chr.2:130746924 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	POTEJ POTEE CYP4F30P GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B TISP43 CFC1 LOC440910
dgv731e199	Chr.2:130678437 - 131300107 on Build GRCh38	Deletion	POTEE CYP4F30P GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B LOC440910
esv2670824	Chr.2:130625264 - 131605218 on Build GRCh38	Deletion	POTEJ GPR148 POTEI PLEKHB2 LINC01120 POTEKP TUBA3D LOC440910 WTH3DI POTEE CYP4F30P MIR4784 ARHGEF4 AMER3 NOC2LP2 FAM168B LOC150776 MZT2A CCDC74A
nsv583136	Chr.2:130730100 - 130846832 on Build GRCh38	Loss	GPR148 POTEI ARHGEF4 AMER3
nsv1014723	Chr.2:130720375 - 131379551 on Build GRCh38	Loss	WTH3DI POTEE GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B LOC440910
nsv1117258	Chr.2:130745687 - 130751923 on Build GRCh38	Tandem Duplication	POTEI
esv3893337	Chr.2:130722838 - 131194387 on Build GRCh38	Loss	GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B
dgv616e201	Chr.2:130674635 - 131312550 on Build GRCh38	Deletion	POTEE CYP4F30P GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B LOC440910
esv3575299	Chr.2:130680940 - 130753107 on Build GRCh38	Gain	CYP4F30P GPR148 POTEI
nsv583135	Chr.2:130724905 - 131194388 on Build GRCh38	Loss	GPR148 POTEI PLEKHB2 ARHGEF4 AMER3 FAM168B
nsv524021	Chr.2:130724906 - 131553515 on Build GRCh38	Loss	GPR148 POTEI PLEKHB2 LINC01120 TUBA3D LOC440910 WTH3DI POTEE MIR4784 ARHGEF4 AMER3 NOC2LP2 FAM168B LOC150776 MZT2A CCDC74A
esv2760576	Chr.2:130634172 - 131521752 on Build GRCh38	Gain+Loss	POTEJ GPR148 POTEI PLEKHB2 LINC01120 TUBA3D LOC440910 WTH3DI POTEE CYP4F30P MIR4784 ARHGEF4 AMER3 NOC2LP2 FAM168B LOC150776 MZT2A
esv2759092	Chr.2:129589265 - 132440430 on Build GRCh38	Gain+Loss	POTEJ POTEF GPR148 POTEKP TUBA3D RAB6C MIR663B NOC2LP2 FAM168B TISP43 MZT2A CCDC74A LOC107985778 PTPN18 NOC2LP1 POTEI LINC01120 CFC1 LINC01087 GPR39 LOC100507460 TUBA3E POTEE CYP4F30P FAR2P2 AMER3 LOC150776 C2orf27B IMP4 ANKRD30BL PLEKHB2 FAM201B CCDC74B MIR4784 ARHGEF4 ZNF806 CFC1B CCDC115 MED15P9 MZT2B SMPD4 LOC389033 C2orf27A LOC440910 FAR2P1 LOC646743 RAB6C-AS1 WTH3DI LOC101927924 CYP4F62P
nsv428403	Chr.2:129818076 - 130882067 on Build GRCh38	Loss	POTEJ POTEF GPR148 RAB6C CCDC74B ARHGEF4 TISP43 CFC1B LOC107985778 CCDC115 PTPN18 MED15P9 MZT2B NOC2LP1 SMPD4 LOC389033 POTEI CFC1 FAR2P1 LOC646743 RAB6C-AS1 TUBA3E LOC101927924 CYP4F30P FAR2P2 CYP4F62P AMER3 IMP4

More Information

Additional Information:

For this assay, SNP(s) [rs111626961] 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