Hs03709649_cn

• Gene Symbol: EGFL7
• Assay Reference Genome Location: Chr.9:136660022 on build GRCh38
• Cytoband: 9q34.3

Target Gene Details

• Entrez Gene ID: 51162
• Gene Name: EGF like domain multiple 7
• Gene Aliases: NEU1, VE-STATIN, ZNEU1
• Location: Chr.9:136654753-136672678 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
EGFL7	NR_046367.1
	XM_011518764.1			XP_011517066.1
	XM_011518765.1			XP_011517067.1
	XM_011518766.1			XP_011517068.1
	XM_011518767.1			XP_011517069.1
	XM_011518768.1			XP_011517070.1
	XM_017014795.1			XP_016870284.1
	XM_017014796.1			XP_016870285.1
	XM_017014797.1			XP_016870286.1
	XM_017014798.1			XP_016870287.1
	XM_017014799.1			XP_016870288.1
	AK091964.1

Target Gene Details

• Entrez Gene ID: 101928612
• Gene Name: uncharacterized LOC101928612
• Gene Aliases: -
• Location: Chr.9:136648610-136660421 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
HSPC324	NR_135132.1
	AF161442.1			AAF29002.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv13005n54	Chr.9:136605258 - 136696482 on Build GRCh38	Loss	EGFL7 LINC01451 AGPAT2 HSPC324 MIR126
nsv509334	Chr.9:136514168 - 136724663 on Build GRCh38	Insertion	EGFL7 FAM69B LINC01451 NOTCH1 SNHG7 MIR4673 AGPAT2 HSPC324 MIR126 MIR4674 NALT1
nsv951203	Chr.9:136562849 - 136770848 on Build GRCh38	Deletion	FAM69B LCN15 LCN6 SNHG7 MIR6722 AGPAT2 HSPC324 MIR126 SNORA17B LOC100128593 EGFL7 LINC01451 SNORA17A LCN10 LCN8
nsv469918	Chr.9:136359865 - 137173890 on Build GRCh38	Loss	FAM69B CCDC183 GRIN1 C9orf142 SNHG7 MIR6722 TMEM141 AGPAT2 C9orf163 SNORA17B SAPCD2 CCDC183-AS1 LINC01451 C9orf172 LCN12 MAN1B1 LCN10 PRR31 MAMDC4 CLIC3 TRAF2 C8G MAN1B1-AS1 UAP1L1 EGFL7 ABCA2 SNORA17A LRRC26 PTGDS EDF1 MIR3621 NOTCH1 INPP5E LCN6 MIR4673 DPP7 HSPC324 PHPT1 LOC100128593 SEC16A MIR4479 PMPCA CARD9 DNLZ MIR4674 MIR4292 LCN8 LCN15 ENTPD2 FBXW5 TMEM210 FUT7 RABL6 SDCCAG3 MIR126 NPDC1 NALT1 LCNL1 SNAPC4 C9orf139 LOC101930307
esv2759720	Chr.9:136356377 - 136932033 on Build GRCh38	Loss	EDF1 FAM69B NOTCH1 CCDC183 INPP5E LCN6 SNHG7 MIR6722 MIR4673 TMEM141 AGPAT2 C9orf163 HSPC324 SNORA17B PHPT1 LOC100128593 CCDC183-AS1 LINC01451 SEC16A MIR4479 C9orf172 PMPCA CARD9 DNLZ MIR4674 MIR4292 LCN10 LCN8 MAMDC4 LCN15 RABL6 SDCCAG3 TRAF2 MIR126 NALT1 EGFL7 SNORA17A SNAPC4 GPSM1
nsv8579	Chr.9:136505432 - 136760256 on Build GRCh38	Gain	FAM69B NOTCH1 LCN15 LCN6 SNHG7 MIR6722 MIR4673 AGPAT2 HSPC324 MIR126 SNORA17B NALT1 LOC100128593 EGFL7 LINC01451 SNORA17A MIR4674 LCN10 LCN8
nsv615971	Chr.9:136583078 - 136670216 on Build GRCh38	Loss	EGFL7 LINC01451 HSPC324
nsv1053781	Chr.9:136590694 - 136722927 on Build GRCh38	Gain	EGFL7 FAM69B LINC01451 AGPAT2 HSPC324 MIR126
dgv957n27	Chr.9:136619086 - 136725859 on Build GRCh38	Loss	EGFL7 FAM69B SNHG7 AGPAT2 HSPC324 MIR126
esv2422220	Chr.9:136584135 - 137350098 on Build GRCh38	Deletion	STPG3 FAM69B CCDC183 GRIN1 C9orf142 SNHG7 MIR6722 TMEM141 AGPAT2 SNORA17B SAPCD2 CCDC183-AS1 LINC01451 C9orf172 LCN12 MAN1B1 TOR4A LCN10 PRR31 MAMDC4 RNF208 CLIC3 TRAF2 C8G MAN1B1-AS1 RNF224 UAP1L1 EGFL7 ABCA2 SNORA17A LRRC26 PTGDS SSNA1 FAM166A ANAPC2 EDF1 C9orf173-AS1 SLC34A3 MIR3621 LCN6 DPP7 HSPC324 TMEM203 PHPT1 LOC100128593 MIR4479 TPRN NRARP NDOR1 MIR4292 LCN8 TUBB4B LCN15 ENTPD2 FBXW5 TMEM210 FUT7 RABL6 MIR126 NPDC1 EXD3 LCNL1 CYSRT1 C9orf139 NELFB LOC101930307

More Information

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

Panther Classification:

Molecular Function -

intercellular signal molecule

Gene Ontology Categories:

Process(es)

angiogenesis
blood vessel development
vasculogenesis
positive regulation of endothelial cell proliferation
cell adhesion
negative regulation of Notch signaling pathway

Function(s)

calcium ion binding