Hs00499893_cn

• Gene Symbol: ELMO3
• Assay Reference Genome Location: Chr.16:67199134 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 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ELMO3	NM_024712.3			NP_078988.2
	AK056923.1
	AK300976.1
	DA872517.1

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

More Information

Additional Information:

For this assay, SNP(s) [rs200422281] 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