Hs05840114_cn

• Gene Symbol: FAM117B
• Assay Reference Genome Location: Chr.2:202640437 on build GRCh38
• Cytoband: 2q33.2

Target Gene Details

• Entrez Gene ID: 150864
• Gene Name: family with sequence similarity 117 member B
• Gene Aliases: ALS2CR13
• Location: Chr.2:202635178-202769757 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM117B	NM_173511.3			NP_775782.2
	AB053315.1			BAB69023.1
	AI523857.1
	AK096090.1			BAC04700.1
	CN397358.1

More Information

Additional Information:

For this assay, SNP(s) [rs114462446,rs79785327] 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, non-DGV Variation

Gene Ontology Categories:

Function(s)

protein binding