Hs03874433_cn

• Gene Symbol: CEP170B
• Assay Reference Genome Location: Chr.14:104874966 on build GRCh38
• Cytoband: 14q32.33

Target Gene Details

• Entrez Gene ID: 283638
• Gene Name: centrosomal protein 170B
• Gene Aliases: CEP170R, FAM68C, KIAA0284
• Location: Chr.14:104865313-104896770 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CEP170B	NM_001112726.2			NP_001106197.1
	NM_015005.2			NP_055820.2
	XM_005267550.3			XP_005267607.1
	XM_011536665.2			XP_011534967.1
	XM_011536666.2			XP_011534968.1
	XM_017021227.1			XP_016876716.1
	XM_017021228.1			XP_016876717.1
	XM_017021229.1			XP_016876718.1
	XM_017021230.1			XP_016876719.1
	AB006622.3
	BC112928.1			AAI12929.1
	BU170784.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv3971n54	Chr.14:104865033 - 104881702 on Build GRCh38	Loss	CEP170B
nsv566099	Chr.14:104818822 - 104946204 on Build GRCh38	Gain	LINC00638 CEP170B AHNAK2 PLD4
esv3635627	Chr.14:104741717 - 104883507 on Build GRCh38	Gain	ZBTB42 SIVA1 LINC00638 AKT1 CEP170B ADSSL1
nsv952272	Chr.14:104843664 - 104889263 on Build GRCh38	Deletion	CEP170B
nsv566137	Chr.14:104865985 - 104893219 on Build GRCh38	Loss	CEP170B
nsv566138	Chr.14:104874306 - 104884018 on Build GRCh38	Loss	CEP170B
nsv470677	Chr.14:104660017 - 104882215 on Build GRCh38	Loss	INF2 ZBTB42 MIR4710 SIVA1 LINC00638 AKT1 CEP170B LOC101929634 ADSSL1 LOC388022
nsv1054574	Chr.14:103210111 - 105365114 on Build GRCh38	Loss	INF2 ZBTB42 LINC00638 CEP170B AHNAK2 TMEM179 APOPT1 ADSSL1 BAG5 PPP1R13B C14orf180 C14orf2 CKB TRMT61A SIVA1 JAG2 BRF1 NUDT14 LOC107984648 MIR6765 LOC105370691 TDRD9 LOC105378183 LOC388022 LOC102723354 AKT1 PACS2 MARK3 GPR132 ZFYVE21 LOC101929634 LINC00637 MIR203A KLC1 MIR4710 EIF5 LOC105370687 BTBD6 LOC105370708 ASPG C14orf79 SNORA28 RD3L PLD4 CDCA4 KIF26A XRCC3 MIR203B

More Information

Additional Information:

For this assay, SNP(s) [rs78369243] 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, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

scaffold/adaptor protein