Assay Details
Target Gene Details
Entrez Gene ID: | 1984 |
Gene Name: | eukaryotic translation initiation factor 5A |
Gene Aliases: |
EIF-5A, EIF5A1, eIF5AI |
Location: |
Chr.17:7306999-7312463 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 7 - Intron 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
EIF5A | NM_001143760.1 | NP_001137232.1 | ||
NM_001143761.1 | NP_001137233.1 | |||
NM_001143762.1 | NP_001137234.1 | |||
NM_001970.4 | NP_001961.1 | |||
XM_005256509.2 | XP_005256566.1 | |||
AF087992.1 | ||||
AK222585.1 | ||||
AK292615.1 | ||||
AY129319.1 | AAN17514.1 | |||
AY129320.1 | AAN17515.1 | |||
AY129321.1 | AAN17516.1 | |||
AY129322.1 | AAN17517.1 | |||
BC000751.2 | AAH00751.1 | |||
BC001832.2 | AAH01832.1 | |||
BC030160.2 | AAH30160.1 | |||
BC080196.1 | AAH80196.1 | |||
BC085015.1 | AAH85015.1 | |||
BC107779.1 | AAI07780.1 | |||
BG479628.1 | ||||
CB111036.1 | ||||
M23419.1 | AAA58453.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2422288 | Chr.17:6789933 - 7646709 on Build GRCh38 | Deletion | FXR2 ACADVL YBX2 SPEM1 MPDU1 EIF4A1 ALOX12P2 SLC35G6 GPS2 ATP1B2 LOC107983988 TNFSF13 TMEM256-PLSCR3 KCTD11 ASGR2 ELP5 TEKT1 DLG4 NEURL4 EIF5A PHF23 PLSCR3 TMEM95 SENP3-EIF4A1 C17orf49 MIR324 FGF11 TMEM102 SNORA48 SLC16A11 CTDNEP1 SLC16A13 CD68 SAT2 TMEM256 NLGN2 CLDN7 BCL6B TNK1 TNFSF12-TNFSF13 DVL2 SHBG C17orf74 TNFSF12 GABARAP ALOX12-AS1 MIR195 SOX15 ASGR1 CHRNB1 SLC2A4 FBXO39 SENP3 RNASEK-C17orf49 CLEC10A ACAP1 SNORD10 ALOX12 LOC100996842 MIR497HG MIR497 SNORA67 POLR2A ZBTB4 RNASEK |
nsv827873 | Chr.17:7309838 - 7311789 on Build GRCh38 | Gain | EIF5A |
esv3639865 | Chr.17:7292786 - 7322537 on Build GRCh38 | Loss | YBX2 NEURL4 EIF5A GPS2 |
nsv960048 | Chr.17:7311126 - 7312422 on Build GRCh38 | Duplication | EIF5A |
nsv509650 | Chr.17:7299079 - 7338714 on Build GRCh38 | Insertion | ACAP1 NEURL4 EIF5A GPS2 |
nsv952118 | Chr.17:7174582 - 7456981 on Build GRCh38 | Deletion | ACADVL YBX2 SPEM1 TMEM256 NLGN2 CLDN7 TNK1 GPS2 DVL2 C17orf74 GABARAP LOC107983988 ASGR1 TMEM256-PLSCR3 CHRNB1 SLC2A4 KCTD11 ELP5 DLG4 ACAP1 NEURL4 EIF5A PHF23 PLSCR3 TMEM95 MIR324 FGF11 TMEM102 CTDNEP1 |
esv2665200 | Chr.17:7091816 - 7333062 on Build GRCh38 | Deletion | ACADVL YBX2 SLC2A4 ASGR2 ELP5 DLG4 CLDN7 NEURL4 EIF5A PHF23 GPS2 DVL2 MIR324 GABARAP CTDNEP1 ASGR1 |
nsv574322 | Chr.17:7010333 - 7689462 on Build GRCh38 | Loss | FXR2 ACADVL YBX2 WRAP53 SPEM1 MPDU1 EIF4A1 SLC35G6 GPS2 ATP1B2 LOC107983988 TNFSF13 TP53 TMEM256-PLSCR3 KCTD11 ASGR2 ELP5 DLG4 NEURL4 EIF5A PHF23 PLSCR3 TMEM95 SENP3-EIF4A1 C17orf49 MIR324 FGF11 TMEM102 SNORA48 SLC16A11 CTDNEP1 SLC16A13 CD68 SAT2 TMEM256 NLGN2 CLDN7 BCL6B TNK1 TNFSF12-TNFSF13 DVL2 SHBG C17orf74 TNFSF12 GABARAP ALOX12-AS1 MIR195 SOX15 ASGR1 CHRNB1 SLC2A4 SENP3 RNASEK-C17orf49 CLEC10A ACAP1 SNORD10 ALOX12 LOC100996842 MIR497HG MIR497 SNORA67 POLR2A ZBTB4 RNASEK |
nsv1963 | Chr.17:7244585 - 7333855 on Build GRCh38 | Deletion | YBX2 SLC2A4 ELP5 CLDN7 NEURL4 EIF5A GPS2 CTDNEP1 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |