Hs00437063_cn

• Gene Symbol: ELMO3
• Assay Reference Genome Location: Chr.16:67203994 on build GRCh38
• Cytoband: 16q22.1

Target Gene Details

• Entrez Gene ID: 79767
• Gene Name: engulfment and cell motility 3
• Gene Aliases: CED-12, CED12, ELMO-3
• Location: Chr.16:67199125-67204024 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 20

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ELMO3	NM_024712.3			NP_078988.2
	AI955864.1
	AK023886.1			BAB14712.1
	AK056923.1	19	2445
	AK300976.1
	BC015524.1			AAH15524.1
	BC034410.1

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	LCAT DPEP2 TRADD NUTF2 CTCF EDC4 GFOD2 LOC105369155 KCTD19 DUS2 DPEP3 FHOD1 ELMO3 PARD6A CARMIL2 PSKH1 HSD11B2 MIR328 ACD C16orf86 SLC12A4 ENKD1 SLC9A5 LRRC36 KIAA0895L ZDHHC1 NRN1L TSNAXIP1 EXOC3L1 ATP6V0D1 NOL3 CENPT FAM65A LRRC29 LOC100505942 LOC100131303 TMEM208 PLEKHG4 FBXL8 LOC107984813 TPPP3 HSF4 E2F4 THAP11 AGRP CTRL PSMB10 RANBP10 DDX28
nsv827707	Chr.16:67148355 - 67289296 on Build GRCh38	Loss	KIAA0895L FHOD1 C16orf70 EXOC3L1 ELMO3 HSF4 B3GNT9 TRADD E2F4 NOL3 MIR328 LOC105369155 LRRC29 TMEM208 PLEKHG4 FBXL8 SLC9A5
nsv952044	Chr.16:67141198 - 67244397 on Build GRCh38	Deletion	KIAA0895L FHOD1 C16orf70 EXOC3L1 ELMO3 HSF4 B3GNT9 TRADD E2F4 NOL3 MIR328 LOC105369155 LRRC29 TMEM208 FBXL8
nsv1160429	Chr.16:67161549 - 67220197 on Build GRCh38	Deletion	KIAA0895L LOC105369155 LRRC29 EXOC3L1 ELMO3 HSF4 FBXL8 E2F4 NOL3 MIR328
nsv524492	Chr.16:67174030 - 67294550 on Build GRCh38	Loss	KIAA0895L FHOD1 EXOC3L1 ELMO3 E2F4 NOL3 MIR328 LOC105369155 KCTD19 LRRC29 TMEM208 PLEKHG4 SLC9A5
nsv524363	Chr.16:67136529 - 68071571 on Build GRCh38	Loss	LCAT DPEP2 B3GNT9 TRADD NUTF2 CTCF EDC4 GFOD2 LOC105369155 KCTD19 DUS2 DPEP3 FHOD1 C16orf70 ELMO3 PARD6A CARMIL2 PSKH1 HSD11B2 MIR328 ACD C16orf86 SLC12A4 ENKD1 SLC9A5 LRRC36 KIAA0895L ZDHHC1 NRN1L TSNAXIP1 EXOC3L1 ATP6V0D1 NOL3 CENPT FAM65A LRRC29 LOC100505942 LOC100131303 TMEM208 PLEKHG4 FBXL8 LOC107984813 TPPP3 HSF4 E2F4 THAP11 AGRP CTRL PSMB10 RANBP10 DDX28
nsv457513	Chr.16:67181417 - 67282697 on Build GRCh38	Loss	KIAA0895L FHOD1 LOC105369155 LRRC29 EXOC3L1 ELMO3 TMEM208 PLEKHG4 E2F4 SLC9A5 MIR328

More Information

Additional Information:

For this assay, SNP(s) [rs114080435,rs116660338] 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, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

scaffold/adaptor protein

Gene Ontology Categories:

Process(es)

phagocytosis
apoptotic process
cell migration

Function(s)

protein binding
SH3 domain binding