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: | Overlaps Exon 3 - Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
EGFL7 | NM_016215.4 | NP_057299.1 | ||
NR_045110.1 | ||||
NR_045111.1 | ||||
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 | ||||
AL512735.1 | CAC21666.1 | |||
AY358902.1 | AAQ89261.1 | |||
AY358903.1 | AAQ89262.1 | |||
BC088371.1 | AAH88371.1 | |||
BI770335.1 | ||||
BX361374.2 |
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 | HSPC324 LINC01451 MIR126 AGPAT2 EGFL7 |
nsv509334 | Chr.9:136514168 - 136724663 on Build GRCh38 | Insertion | HSPC324 SNHG7 LINC01451 MIR4673 NOTCH1 NALT1 MIR126 AGPAT2 EGFL7 MIR4674 FAM69B |
nsv951203 | Chr.9:136562849 - 136770848 on Build GRCh38 | Deletion | LCN10 LINC01451 LCN15 LOC100128593 FAM69B SNORA17A HSPC324 SNHG7 SNORA17B MIR6722 LCN8 LCN6 MIR126 AGPAT2 EGFL7 |
nsv469918 | Chr.9:136359865 - 137173890 on Build GRCh38 | Loss | C8G PHPT1 LCN15 LRRC26 CCDC183 MAN1B1 SNORA17A ENTPD2 NALT1 C9orf163 MIR126 CLIC3 MAN1B1-AS1 RABL6 CCDC183-AS1 EGFL7 MIR3621 LCN12 MAMDC4 EDF1 TMEM141 HSPC324 INPP5E SNHG7 SDCCAG3 C9orf142 MIR4673 NPDC1 NOTCH1 UAP1L1 AGPAT2 CARD9 LCN10 C9orf139 LINC01451 GRIN1 DNLZ MIR4479 LCNL1 LOC101930307 SNAPC4 SNORA17B C9orf172 PRR31 MIR4674 ABCA2 DPP7 FBXW5 MIR4292 TMEM210 LOC100128593 FAM69B PTGDS SEC16A FUT7 MIR6722 LCN8 TRAF2 LCN6 SAPCD2 PMPCA |
esv2759720 | Chr.9:136356377 - 136932033 on Build GRCh38 | Loss | LCN10 PHPT1 LINC01451 LCN15 DNLZ MIR4479 CCDC183 SNORA17A SNAPC4 SNORA17B C9orf172 NALT1 C9orf163 MIR126 RABL6 CCDC183-AS1 EGFL7 MIR4674 GPSM1 MIR4292 MAMDC4 LOC100128593 FAM69B EDF1 TMEM141 HSPC324 INPP5E SNHG7 SDCCAG3 SEC16A MIR4673 NOTCH1 MIR6722 LCN8 TRAF2 LCN6 PMPCA AGPAT2 CARD9 |
nsv8579 | Chr.9:136505432 - 136760256 on Build GRCh38 | Gain | LCN10 LINC01451 LCN15 LOC100128593 FAM69B SNORA17A HSPC324 SNHG7 SNORA17B MIR4673 NOTCH1 MIR6722 LCN8 NALT1 LCN6 MIR126 AGPAT2 EGFL7 MIR4674 |
nsv615971 | Chr.9:136583078 - 136670216 on Build GRCh38 | Loss | HSPC324 LINC01451 EGFL7 |
nsv1053781 | Chr.9:136590694 - 136722927 on Build GRCh38 | Gain | HSPC324 LINC01451 MIR126 AGPAT2 EGFL7 FAM69B |
dgv957n27 | Chr.9:136619086 - 136725859 on Build GRCh38 | Loss | HSPC324 SNHG7 MIR126 AGPAT2 EGFL7 FAM69B |
esv2422220 | Chr.9:136584135 - 137350098 on Build GRCh38 | Deletion | C8G PHPT1 SLC34A3 LCN15 LRRC26 CCDC183 MAN1B1 SNORA17A ENTPD2 TOR4A ANAPC2 RNF224 EXD3 MIR126 CLIC3 MAN1B1-AS1 RABL6 CCDC183-AS1 EGFL7 RNF208 STPG3 NELFB MIR3621 LCN12 MAMDC4 TUBB4B EDF1 TMEM141 HSPC324 SNHG7 C9orf142 NRARP NPDC1 UAP1L1 AGPAT2 TMEM203 SSNA1 LCN10 C9orf139 LINC01451 GRIN1 MIR4479 LCNL1 LOC101930307 C9orf173-AS1 SNORA17B NDOR1 C9orf172 PRR31 FAM166A ABCA2 DPP7 FBXW5 TPRN MIR4292 CYSRT1 TMEM210 LOC100128593 FAM69B PTGDS FUT7 MIR6722 LCN8 TRAF2 LCN6 SAPCD2 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |