Assay Details
Target Gene Details
Entrez Gene ID: | 4335 |
Gene Name: | MAX network transcriptional repressor |
Gene Aliases: |
MAD6, MXD6, ROX, bHLHd3 |
Location: |
Chr.17:2384060-2400964 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MNT | NM_020310.2 | 5 | 1125 | NP_064706.1 |
XM_011523868.2 | 5 | 1062 | XP_011522170.1 | |
XM_011523869.1 | 2 | 159 | XP_011522171.1 | |
XM_017024654.1 | 2 | 2771 | XP_016880143.1 | |
AK291596.1 | 5 | 1222 | ||
BC117563.1 | 5 | 875 | AAI17564.1 | |
X96401.1 | 5 | 1085 | CAA65265.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833338 | Chr.17:2363607 - 2592205 on Build GRCh38 | Loss | MNT LOC101927864 METTL16 LOC284009 SGSM2 |
nsv470569 | Chr.17:2359409 - 2395680 on Build GRCh38 | Loss | MNT LOC101927864 SGSM2 |
nsv1063109 | Chr.17:2342302 - 2591288 on Build GRCh38 | Gain | MNT LOC101927864 METTL16 LOC284009 SGSM2 |
nsv469765 | Chr.17:2213155 - 2400446 on Build GRCh38 | Loss | LOC101927839 SNORD91A TSR1 MNT LOC101927864 SRR SMG6 SNORD91B SGSM2 |
nsv952104 | Chr.17:2337907 - 2399506 on Build GRCh38 | Deletion | MNT LOC101927864 SGSM2 |
nsv1160444 | Chr.17:2377640 - 2402666 on Build GRCh38 | Deletion | MNT SGSM2 |
nsv1160443 | Chr.17:2346610 - 2406836 on Build GRCh38 | Deletion | MNT LOC101927864 SGSM2 |
nsv1066475 | Chr.17:2359823 - 2390866 on Build GRCh38 | Loss | MNT LOC101927864 SGSM2 |
dgv3083n100 | Chr.17:2351844 - 2409068 on Build GRCh38 | Gain | MNT LOC101927864 LOC284009 SGSM2 |
nsv833336 | Chr.17:2176922 - 2400456 on Build GRCh38 | Loss | LOC101927839 SNORD91A TSR1 MNT LOC101927864 SRR SMG6 SNORD91B SGSM2 |
nsv574224 | Chr.17:2269769 - 2423186 on Build GRCh38 | Gain | SNORD91A TSR1 MNT LOC101927864 SRR SMG6 METTL16 SNORD91B LOC284009 SGSM2 |
nsv517489 | Chr.17:2344688 - 2395680 on Build GRCh38 | Loss | MNT LOC101927864 SGSM2 |
nsv1055225 | Chr.17:2343962 - 2389565 on Build GRCh38 | Loss | MNT LOC101927864 SGSM2 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |