Hs05440964_cn

• Gene Symbol: FAM192A
• Assay Reference Genome Location: Chr.16:57170491 on build GRCh38
• Cytoband: 16q13

Target Gene Details

• Entrez Gene ID: 80011
• Gene Name: family with sequence similarity 192 member A
• Gene Aliases: C16orf94, CDA018, CDA10, NIP30
• Location: Chr.16:57152466-57186242 on Build GRCh38
• Assay Gene Location: Within Intron 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM192A	NM_024946.2			NP_079222.1
	XM_005256156.4			XP_005256213.1
	XM_005256158.3			XP_005256215.1
	XM_005256160.2			XP_005256217.1
	XM_005256163.2			XP_005256220.1
	XM_005256164.3			XP_005256221.1
	XM_005256165.2			XP_005256222.1
	XM_006721275.3			XP_006721338.2
	XM_011523343.2			XP_011521645.1
	XM_017023681.1			XP_016879170.1
	XM_017023682.1			XP_016879171.1
	XM_017023683.1			XP_016879172.1
	XM_017023684.1			XP_016879173.1
	XM_017023685.1			XP_016879174.1
	XM_017023686.1			XP_016879175.1
	XM_017023687.1			XP_016879176.1
	XM_017023688.1			XP_016879177.1
	XM_017023689.1			XP_016879178.1
	XM_017023690.1			XP_016879179.1
	XM_017023691.1			XP_016879180.1
	XM_017023692.1			XP_016879181.1
	XM_017023693.1			XP_016879182.1
	XM_017023694.1			XP_016879183.1
	XM_017023695.1			XP_016879184.1
	XM_017023696.1			XP_016879185.1
	XM_017023697.1			XP_016879186.1
	XM_017023698.1			XP_016879187.1
	XM_017023699.1			XP_016879188.1
	XM_017023700.1			XP_016879189.1
	XM_017023701.1			XP_016879190.1
	XM_017023702.1			XP_016879191.1
	XM_017023703.1			XP_016879192.1
	XM_017023704.1			XP_016879193.1
	AF212249.1			AAK14932.1
	AF271785.1			AAG44796.1
	AF356585.1			AAK43697.1
	AK023291.1			BAB14512.1
	AK025452.1			BAB15136.1
	AL834421.1			CAD39082.1
	BC020536.1			AAH20536.1
	BC063409.1			AAH63409.1
	BC071952.1			AAH71952.1

More Information

Additional Information:

For this assay, SNP(s) [rs116735523] 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