Assay Details
Target Gene Details
Entrez Gene ID: | 8515 |
Gene Name: | integrin subunit alpha 10 |
Gene Aliases: |
PRO827 |
Location: |
Chr.1:145891208-145910189 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 27 - Intron 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ITGA10 | NM_001303040.1 | NP_001289969.1 | ||
NM_001303041.1 | NP_001289970.1 | |||
NM_003637.4 | NP_003628.2 | |||
XM_005277436.3 | XP_005277493.1 | |||
XM_011510083.2 | XP_011508385.1 | |||
XM_011510084.1 | XP_011508386.1 | |||
XM_017002622.1 | XP_016858111.1 | |||
XM_017002623.1 | XP_016858112.1 | |||
XM_017002624.1 | XP_016858113.1 | |||
XM_017002625.1 | XP_016858114.1 | |||
XM_017002626.1 | XP_016858115.1 | |||
XM_017002628.1 | XP_016858117.1 | |||
AF074015.1 | AAC31952.1 | |||
AF112345.1 | AAF21944.1 | |||
AK304155.1 | ||||
AK304183.1 | ||||
AK314255.1 | ||||
BC140831.1 | ||||
BC144637.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1005055 | Chr.1:145642988 - 148991068 on Build GRCh38 | Loss | NBPF11 NUDT4P1 MIR6736 RNVU1-3 CHD1L PDZK1P1 LIX1L RNVU1-6 ANKRD34A ITGA10 PEX11B HFE2 NUDT4P2 RNVU1-8 LOC100996763 PRKAB2 POLR3GL NBPF13P GPR89A LOC728989 POLR3C LOC101927468 LINC01138 PDIA3P1 ANKRD35 ACP6 LOC100505824 LOC100996517 HYDIN2 RNVU1-1 PPIAL4G GNRHR2 CD160 LOC105371226 PDE4DIP GJA5 CH17-408M7.1 NBPF10 LOC284561 RBM8A GJA8 BCL9 LOC100132057 MIR6077 NUDT17 PIAS3 GPR89B RNVU1-7 TXNIP RNF115 LOC101928979 MIR5087 LOC105371242 NBPF14 PDZK1 RNU1-13P LINC00624 NBPF12 FMO5 NOTCH2NL |
esv3587420 | Chr.1:145824369 - 145905171 on Build GRCh38 | Gain | MIR6736 ANKRD35 POLR3C NUDT17 PIAS3 ITGA10 |
nsv831381 | Chr.1:145784568 - 145960930 on Build GRCh38 | Gain | POLR3GL MIR6736 GNRHR2 RNF115 LIX1L POLR3C ANKRD34A ITGA10 PEX11B ANKRD35 RBM8A NUDT17 PIAS3 |
esv3587419 | Chr.1:145893340 - 145919968 on Build GRCh38 | Gain | PEX11B GNRHR2 ITGA10 |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |