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 4 |
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 | |||
AB125649.1 | BAD01469.1 | |||
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 MIR126 LINC01451 EGFL7 AGPAT2 |
nsv509334 | Chr.9:136514168 - 136724663 on Build GRCh38 | Insertion | HSPC324 SNHG7 MIR4673 MIR126 LINC01451 NOTCH1 MIR4674 EGFL7 NALT1 AGPAT2 FAM69B |
nsv951203 | Chr.9:136562849 - 136770848 on Build GRCh38 | Deletion | LCN8 SNHG7 MIR126 LINC01451 MIR6722 LOC100128593 AGPAT2 SNORA17B HSPC324 LCN6 LCN15 LCN10 SNORA17A EGFL7 FAM69B |
nsv469918 | Chr.9:136359865 - 137173890 on Build GRCh38 | Loss | LRRC26 NOTCH1 UAP1L1 PTGDS NALT1 CCDC183 SNORA17B C9orf142 ABCA2 FUT7 CCDC183-AS1 C9orf139 C9orf163 NPDC1 SNORA17A EGFL7 SNAPC4 TMEM210 MAMDC4 LINC01451 MIR6722 LOC100128593 TRAF2 PHPT1 AGPAT2 FBXW5 DPP7 MIR4292 HSPC324 CARD9 SEC16A GRIN1 C9orf172 FAM69B DNLZ SNHG7 MIR4673 MIR126 ENTPD2 SDCCAG3 MIR4674 MAN1B1-AS1 MAN1B1 PRR31 MIR3621 INPP5E LCN6 LCNL1 C8G LCN10 EDF1 LOC101930307 SAPCD2 LCN12 LCN8 MIR4479 PMPCA RABL6 TMEM141 LCN15 CLIC3 |
esv2759720 | Chr.9:136356377 - 136932033 on Build GRCh38 | Loss | DNLZ SNHG7 MIR4673 MIR126 NOTCH1 SDCCAG3 MIR4674 NALT1 CCDC183 SNORA17B INPP5E LCN6 CCDC183-AS1 C9orf163 LCN10 SNORA17A EGFL7 EDF1 SNAPC4 LCN8 MIR4479 PMPCA MAMDC4 LINC01451 MIR6722 LOC100128593 TRAF2 PHPT1 AGPAT2 RABL6 MIR4292 HSPC324 CARD9 SEC16A TMEM141 C9orf172 LCN15 GPSM1 FAM69B |
nsv8579 | Chr.9:136505432 - 136760256 on Build GRCh38 | Gain | LCN8 SNHG7 MIR4673 MIR126 LINC01451 NOTCH1 MIR6722 LOC100128593 MIR4674 NALT1 AGPAT2 SNORA17B HSPC324 LCN6 LCN15 LCN10 SNORA17A EGFL7 FAM69B |
nsv615971 | Chr.9:136583078 - 136670216 on Build GRCh38 | Loss | HSPC324 LINC01451 EGFL7 |
nsv1053781 | Chr.9:136590694 - 136722927 on Build GRCh38 | Gain | HSPC324 MIR126 LINC01451 EGFL7 AGPAT2 FAM69B |
dgv957n27 | Chr.9:136619086 - 136725859 on Build GRCh38 | Loss | HSPC324 SNHG7 MIR126 EGFL7 AGPAT2 FAM69B |
esv2422220 | Chr.9:136584135 - 137350098 on Build GRCh38 | Deletion | NELFB LRRC26 TUBB4B UAP1L1 PTGDS FAM166A CCDC183 SNORA17B C9orf142 ABCA2 FUT7 CCDC183-AS1 C9orf139 NPDC1 NDOR1 SNORA17A EGFL7 TMEM210 MAMDC4 LINC01451 MIR6722 LOC100128593 TRAF2 PHPT1 AGPAT2 FBXW5 DPP7 MIR4292 HSPC324 GRIN1 C9orf172 FAM69B EXD3 SNHG7 MIR126 ENTPD2 MAN1B1-AS1 MAN1B1 PRR31 MIR3621 C9orf173-AS1 LCN6 LCNL1 TPRN TOR4A C8G LCN10 SLC34A3 STPG3 EDF1 LOC101930307 SAPCD2 LCN12 LCN8 MIR4479 CYSRT1 SSNA1 ANAPC2 RABL6 RNF224 NRARP TMEM141 LCN15 TMEM203 CLIC3 RNF208 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |