Assay Details
Target Gene Details
Entrez Gene ID: | 7965 |
Gene Name: | aminoacyl tRNA synthetase complex interacting multifunctional protein 2 |
Gene Aliases: |
JTV-1, JTV1, P38 |
Location: |
Chr.7:6009241-6023834 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
AIMP2 | NM_001326606.1 | NP_001313535.1 | ||
NM_001326607.1 | NP_001313536.1 | |||
NM_001326609.1 | NP_001313538.1 | |||
NM_001326611.1 | NP_001313540.1 | |||
NM_006303.3 | NP_006294.2 | |||
XM_005249847.3 | XP_005249904.1 | |||
XM_005249848.2 | XP_005249905.1 | |||
XM_005249850.3 | XP_005249907.1 | |||
XM_006715772.2 | XP_006715835.1 | |||
XM_011515519.1 | XP_011513821.1 | |||
AK313037.1 | ||||
BC002853.1 | AAH02853.1 | |||
BC010156.1 | AAH10156.1 | |||
BC013630.1 | AAH13630.1 | |||
CX867709.1 | ||||
U24169.1 | AAC50391.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1034916 | Chr.7:5895149 - 6119339 on Build GRCh38 | Gain | USP42 CCZ1 PMS2 RSPH10B AIMP2 EIF2AK1 ANKRD61 |
nsv436904 | Chr.7:5035574 - 6713282 on Build GRCh38 | Insertion | USP42 CCZ1 ZNF890P FBXL18 DAGLB ZDHHC4 RNF216-IT1 LOC100419773 LOC221946 EIF2AK1 ANKRD61 RBAKDN CYTH3 RBAK-RBAKDN ACTB LOC107986762 OCM KDELR2 LOC100129484 C7orf26 ZNF815P RNF216 FSCN1 MIR6874 WIPI2 ZNF853 ZNF316 MIR589 TNRC18 ZNF12 FAM220A GRID2IP PMS2 RSPH10B AIMP2 RBAK RAC1 SLC29A4 |
nsv830894 | Chr.7:5850027 - 6032584 on Build GRCh38 | Loss | CCZ1 ZNF815P PMS2 RSPH10B AIMP2 OCM EIF2AK1 ANKRD61 |
nsv605998 | Chr.7:5995434 - 6062403 on Build GRCh38 | Loss | PMS2 AIMP2 EIF2AK1 ANKRD61 |
dgv6241n100 | Chr.7:5709351 - 6016988 on Build GRCh38 | Gain | CCZ1 ZNF815P RNF216 PMS2 RSPH10B AIMP2 MIR6874 OCM |
esv3612009 | Chr.7:6015386 - 6020307 on Build GRCh38 | Gain | AIMP2 |
nsv1018388 | Chr.7:5999082 - 6091538 on Build GRCh38 | Gain | USP42 PMS2 AIMP2 EIF2AK1 ANKRD61 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |