Hs06303067_cn

• Gene Symbol: FAM168A
• Assay Reference Genome Location: Chr.11:73402453 on build GRCh38
• Cytoband: 11q13.4

Target Gene Details

• Entrez Gene ID: 23201
• Gene Name: family with sequence similarity 168 member A
• Gene Aliases: KIAA0280, TCRP1
• Location: Chr.11:73400478-73598189 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM168A	NM_001286050.1	9	5330	NP_001272979.1
	NM_001286051.1	6	4985	NP_001272980.1
	NM_015159.2	8	5303	NP_055974.1
	XM_017017415.1	6	4910	XP_016872904.1
	XM_017017416.1	6	4745	XP_016872905.1
	D87470.1	9	5187

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv951041	Chr.11:73336156 - 73402655 on Build GRCh38	Deletion	RELT FAM168A ARHGEF17

More Information

Additional Information:

For this assay, SNP(s) [rs150370782] 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, Exonic, DGV Variation

Panther Classification:

Molecular Function -

myelin protein

Gene Ontology Categories:

Function(s)

protein binding