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