Hs06180372_cn

• Gene Symbol: FAM167A
• Assay Reference Genome Location: Chr.8:11443038 on build GRCh38
• Cytoband: 8p23.1

Target Gene Details

• Entrez Gene ID: 83648
• Gene Name: family with sequence similarity 167 member A
• Gene Aliases: C8orf13, D8S265
• Location: Chr.8:11421464-11475904 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM167A	NM_053279.2			NP_444509.2
	XM_005272398.4			XP_005272455.1
	XM_011543837.1			XP_011542139.1
	XM_011543838.2			XP_011542140.1
	XM_011543840.2			XP_011542142.1
	AJ301564.1			CAC82740.1
	AK290704.1
	AL157475.1			CAB75670.1
	AL834122.1			CAD38843.1
	BC048214.1			AAH48214.1
	BC104041.1			AAI04042.1
	BC104042.1			AAI04043.1
	BC104043.1			AAI04044.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv951100	Chr.8:11442292 - 11457691 on Build GRCh38	Deletion	FAM167A
esv34097	Chr.8:11319863 - 11632385 on Build GRCh38	Loss	TDH SLC35G5 LINC00208 BLK MTMR9 FAM167A FAM167A-AS1 LOC101929290
nsv509252	Chr.8:11419836 - 11481229 on Build GRCh38	Insertion	FAM167A FAM167A-AS1
nsv1030756	Chr.8:11434564 - 11475273 on Build GRCh38	Gain	FAM167A FAM167A-AS1
nsv522860	Chr.8:11396370 - 11472855 on Build GRCh38	Loss	FAM167A FAM167A-AS1
nsv465465	Chr.8:11387555 - 11449609 on Build GRCh38	Loss	FAM167A FAM167A-AS1
nsv470183	Chr.8:11379466 - 11449609 on Build GRCh38	Loss	FAM167A FAM167A-AS1

More Information

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

Gene Ontology Categories:

Function(s)

protein binding