Hs03501358_cn

• Gene Symbol: FAM200B
• Assay Reference Genome Location: Chr.4:15682959 on build GRCh38
• Cytoband: 4p15.32

Target Gene Details

• Entrez Gene ID: 285550
• Gene Name: family with sequence similarity 200 member B
• Gene Aliases: -
• Location: Chr.4:15681729-15690447 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM200B	NM_001145191.1			NP_001138663.1
	XM_017008048.1			XP_016863537.1
	DA408954.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv315n21	Chr.4:15609148 - 15690513 on Build GRCh38	Loss	BST1 FBXL5 FAM200B
nsv949802	Chr.4:15647778 - 15695177 on Build GRCh38	Duplication	BST1 FBXL5 FAM200B
nsv428439	Chr.4:15555338 - 15747897 on Build GRCh38	Gain+Loss	BST1 CC2D2A FBXL5 FAM200B
esv2759227	Chr.4:15442993 - 15747897 on Build GRCh38	Gain+Loss	BST1 CC2D2A FBXL5 FAM200B C1QTNF7

More Information

Additional Information:

For this assay, SNP(s) [rs111623988] 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

Gene Ontology Categories:

Process(es)

regulation of transcription from RNA polymerase II promoter

Function(s)

RNA polymerase II transcription factor activity, sequence-specific DNA binding
DNA binding