Hs03026747_cn

• Gene Symbol: FHOD1
• Assay Reference Genome Location: Chr.16:67234096 on build GRCh38
• Cytoband: 16q22.1

Target Gene Details

• Entrez Gene ID: 29109
• Gene Name: formin homology 2 domain containing 1
• Gene Aliases: FHOS
• Location: Chr.16:67229389-67247522 on Build GRCh38
• Assay Gene Location: Within Exon 17

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FHOD1	NM_001318202.1	15	1797	NP_001305131.1
	NM_013241.2	13	1719	NP_037373.2
	XM_006721180.1	4	372	XP_006721243.1
	XM_011523043.2	15	2013	XP_011521345.1
	XM_011523044.1	15	1742	XP_011521346.1
	XM_011523045.2	15	1507	XP_011521347.1
	AB041046.1	13	1689	BAD06250.1
	AB209584.1	11	2188	BAD92821.1
	AF113615.1	13	1625	AAD39906.1
	AK301157.1	3	430
	AK304232.1	13	1654
	AY192154.1	13	1607	AAO38757.1
	BC033084.1	13	1664	AAH33084.1
	KJ658417.1	15	1685

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv522852	Chr.16:67153308 - 68071571 on Build GRCh38	Gain	LOC107984813 TSNAXIP1 C16orf86 FAM65A TRADD SLC12A4 KCTD19 LCAT LOC100505942 LRRC36 LOC105369155 DDX28 MIR328 ATP6V0D1 AGRP NRN1L TMEM208 CTRL NUTF2 GFOD2 PLEKHG4 ELMO3 FHOD1 DUS2 E2F4 LRRC29 CTCF ACD LOC100131303 RANBP10 HSD11B2 THAP11 KIAA0895L PSKH1 CENPT PARD6A DPEP3 ENKD1 FBXL8 NOL3 EXOC3L1 ZDHHC1 TPPP3 HSF4 PSMB10 DPEP2 EDC4 SLC9A5 CARMIL2
nsv827707	Chr.16:67148355 - 67289296 on Build GRCh38	Loss	MIR328 TMEM208 KIAA0895L TRADD C16orf70 PLEKHG4 HSF4 ELMO3 FBXL8 FHOD1 NOL3 E2F4 B3GNT9 LRRC29 LOC105369155 EXOC3L1 SLC9A5
nsv952044	Chr.16:67141198 - 67244397 on Build GRCh38	Deletion	MIR328 TMEM208 KIAA0895L TRADD C16orf70 HSF4 ELMO3 FBXL8 FHOD1 NOL3 E2F4 B3GNT9 LRRC29 LOC105369155 EXOC3L1
nsv457513	Chr.16:67181417 - 67282697 on Build GRCh38	Loss	PLEKHG4 MIR328 ELMO3 FHOD1 E2F4 TMEM208 LRRC29 LOC105369155 EXOC3L1 SLC9A5 KIAA0895L
nsv524492	Chr.16:67174030 - 67294550 on Build GRCh38	Loss	MIR328 TMEM208 KIAA0895L KCTD19 PLEKHG4 ELMO3 FHOD1 NOL3 E2F4 LRRC29 LOC105369155 EXOC3L1 SLC9A5
nsv524363	Chr.16:67136529 - 68071571 on Build GRCh38	Loss	LOC107984813 TSNAXIP1 C16orf86 FAM65A TRADD C16orf70 SLC12A4 KCTD19 LCAT LOC100505942 LRRC36 LOC105369155 DDX28 MIR328 ATP6V0D1 AGRP NRN1L TMEM208 CTRL NUTF2 GFOD2 PLEKHG4 ELMO3 FHOD1 DUS2 E2F4 B3GNT9 LRRC29 CTCF ACD LOC100131303 RANBP10 HSD11B2 THAP11 KIAA0895L PSKH1 CENPT PARD6A DPEP3 ENKD1 FBXL8 NOL3 EXOC3L1 ZDHHC1 TPPP3 HSF4 PSMB10 DPEP2 EDC4 SLC9A5 CARMIL2

More Information

Additional Information:

For this assay, SNP(s) [rs77958237] 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, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

positive regulation of transcription from RNA polymerase II promoter
positive regulation of stress fiber assembly

Function(s)

actin binding
protein binding
identical protein binding