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