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 | AGPAT2 LINC01451 MIR126 EGFL7 HSPC324 |
nsv509334 | Chr.9:136514168 - 136724663 on Build GRCh38 | Insertion | AGPAT2 LINC01451 MIR126 FAM69B MIR4673 MIR4674 EGFL7 HSPC324 NOTCH1 NALT1 SNHG7 |
nsv951203 | Chr.9:136562849 - 136770848 on Build GRCh38 | Deletion | AGPAT2 MIR126 LCN6 SNORA17B LOC100128593 SNHG7 LCN10 LINC01451 LCN15 FAM69B MIR6722 EGFL7 HSPC324 SNORA17A LCN8 |
nsv469918 | Chr.9:136359865 - 137173890 on Build GRCh38 | Loss | AGPAT2 MIR126 SEC16A MIR3621 MIR4292 MIR4479 LCN6 C9orf163 SNORA17B C9orf139 SNAPC4 DNLZ C8G ABCA2 LCN12 FAM69B MIR4673 LCNL1 EDF1 MAN1B1 C9orf142 FBXW5 PTGDS MAMDC4 DPP7 LCN10 MAN1B1-AS1 CCDC183-AS1 LCN15 INPP5E MIR6722 LRRC26 TMEM141 CARD9 GRIN1 TRAF2 LOC100128593 ENTPD2 SNHG7 LINC01451 PMPCA HSPC324 NALT1 SAPCD2 NPDC1 CCDC183 C9orf172 MIR4674 UAP1L1 NOTCH1 LOC101930307 TMEM210 RABL6 PRR31 CLIC3 EGFL7 PHPT1 SDCCAG3 FUT7 SNORA17A LCN8 |
esv2759720 | Chr.9:136356377 - 136932033 on Build GRCh38 | Loss | AGPAT2 TMEM141 CARD9 MIR126 SEC16A MIR4292 MIR4479 LCN6 C9orf163 TRAF2 SNORA17B LOC100128593 SNAPC4 DNLZ SNHG7 LINC01451 FAM69B MIR4673 PMPCA HSPC324 GPSM1 NALT1 CCDC183 C9orf172 EDF1 MIR4674 NOTCH1 MAMDC4 LCN10 CCDC183-AS1 LCN15 RABL6 INPP5E MIR6722 EGFL7 PHPT1 SDCCAG3 SNORA17A LCN8 |
nsv8579 | Chr.9:136505432 - 136760256 on Build GRCh38 | Gain | AGPAT2 MIR126 MIR4674 LCN6 SNORA17B LOC100128593 NOTCH1 SNHG7 LCN10 LINC01451 LCN15 FAM69B MIR6722 MIR4673 EGFL7 HSPC324 NALT1 SNORA17A LCN8 |
nsv615971 | Chr.9:136583078 - 136670216 on Build GRCh38 | Loss | LINC01451 EGFL7 HSPC324 |
nsv1053781 | Chr.9:136590694 - 136722927 on Build GRCh38 | Gain | AGPAT2 LINC01451 MIR126 FAM69B EGFL7 HSPC324 |
dgv957n27 | Chr.9:136619086 - 136725859 on Build GRCh38 | Loss | AGPAT2 MIR126 FAM69B EGFL7 HSPC324 SNHG7 |
esv2422220 | Chr.9:136584135 - 137350098 on Build GRCh38 | Deletion | AGPAT2 MIR126 CYSRT1 NRARP MIR3621 MIR4292 MIR4479 LCN6 SNORA17B C9orf139 C8G ABCA2 LCN12 FAM69B LCNL1 TOR4A TPRN ANAPC2 EDF1 MAN1B1 C9orf142 FBXW5 PTGDS MAMDC4 DPP7 LCN10 MAN1B1-AS1 CCDC183-AS1 LCN15 SLC34A3 MIR6722 NELFB TMEM203 LRRC26 TMEM141 GRIN1 TUBB4B TRAF2 LOC100128593 ENTPD2 SNHG7 SSNA1 C9orf173-AS1 LINC01451 HSPC324 STPG3 FAM166A SAPCD2 RNF224 NPDC1 NDOR1 CCDC183 C9orf172 RNF208 UAP1L1 LOC101930307 TMEM210 RABL6 PRR31 CLIC3 EGFL7 PHPT1 FUT7 EXD3 SNORA17A LCN8 |
More Information
Additional Information:
For this assay, SNP(s) [rs75759763] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |