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