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
nsv566099	Chr.14:104818822 - 104946204 on Build GRCh38	Gain	CEP170B LINC00638 PLD4 AHNAK2
dgv3971n54	Chr.14:104865033 - 104881702 on Build GRCh38	Loss	CEP170B
esv3635627	Chr.14:104741717 - 104883507 on Build GRCh38	Gain	CEP170B SIVA1 LINC00638 ZBTB42 AKT1 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	CEP170B MIR4710 SIVA1 LOC388022 LINC00638 ZBTB42 AKT1 INF2 LOC101929634 ADSSL1
nsv1054574	Chr.14:103210111 - 105365114 on Build GRCh38	Loss	JAG2 MIR203A LINC00638 LOC107984648 APOPT1 LOC102723354 GPR132 MARK3 INF2 MIR6765 CKB XRCC3 ADSSL1 EIF5 LOC105370687 CEP170B KIF26A BRF1 RD3L ZBTB42 LOC105370708 TMEM179 PACS2 PLD4 LOC101929634 SIVA1 LOC388022 TRMT61A TDRD9 LINC00637 ASPG SNORA28 CDCA4 C14orf2 BTBD6 MIR4710 PPP1R13B MIR203B C14orf79 LOC105378183 NUDT14 KLC1 ZFYVE21 AKT1 C14orf180 AHNAK2 BAG5 LOC105370691

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