Hs05223248_cn

• Gene Symbol: FAM13C
• Assay Reference Genome Location: Chr.10:59263404 on build GRCh38
• Cytoband: 10q21.1

Target Gene Details

• Entrez Gene ID: 220965
• Gene Name: family with sequence similarity 13 member C
• Gene Aliases: FAM13C1
• Location: Chr.10:59245933-59363186 on Build GRCh38
• Assay Gene Location: Within Intron 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM13C	NM_001001971.2			NP_001001971.1
	NM_001143773.1			NP_001137245.1
	NM_001166698.1			NP_001160170.1
	NM_198215.3			NP_937858.2
	XM_005269618.4			XP_005269675.2
	XM_005269619.4			XP_005269676.2
	XM_006717702.3			XP_006717765.1
	XM_006717703.3			XP_006717766.1
	XM_011539490.2			XP_011537792.1
	XM_011539491.2			XP_011537793.1
	XM_017015885.1			XP_016871374.1
	XM_017015886.1			XP_016871375.1
	XM_017015887.1			XP_016871376.1
	XM_017015888.1			XP_016871377.1
	XM_017015889.1			XP_016871378.1
	XM_017015890.1			XP_016871379.1
	XM_017015891.1			XP_016871380.1
	XM_017015892.1			XP_016871381.1
	XM_017015893.1			XP_016871382.1
	AK289796.1
	AK294805.1
	AK299924.1
	AK316542.1
	BC036453.1			AAH36453.1
	BC064431.1			AAH64431.1
	U79304.1			AAB50228.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv831888	Chr.10:59183895 - 59378493 on Build GRCh38	Gain	FAM13C PHYHIPL

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

protein binding