Genomic Map
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Target Gene Details
Entrez Gene ID: | 196743 |
Gene Name: | polyamine oxidase (exo-N4-amino) |
Gene Aliases: |
PAO |
Location: |
Chr.10:133379237-133391696 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PAOX | NM_152911.3 | 3 | 903 | NP_690875.1 |
| NM_207127.2 | 3 | 903 | NP_997010.1 | |
| NM_207128.2 | 3 | 903 | NP_997011.1 | |
| NR_109763.1 | 3 | 903 | ||
| NR_109764.1 | 2 | 416 | ||
| NR_109765.1 | 2 | 416 | ||
| NR_109766.1 | 2 | 416 | ||
| AF226657.1 | 2 | 643 | AAN40706.1 | |
| AF312698.1 | 3 | 949 | AAO63265.1 | |
| AK124186.1 | ||||
| AK128001.1 | 3 | 787 | ||
| AL834535.1 | 1 | 148 | CAD39191.1 | |
| AY358418.1 | 3 | 843 | AAQ88784.1 | |
| AY541513.1 | 3 | 853 | AAS64373.1 | |
| AY541514.1 | 2 | 366 | AAS64374.1 | |
| AY541515.1 | 3 | 853 | AAS64375.1 | |
| AY541516.1 | 3 | 879 | AAS64376.1 | |
| AY541517.1 | 2 | 365 | AAS64377.1 | |
| AY541518.1 | 2 | 366 | AAS64378.1 | |
| AY541519.1 | 3 | 853 | AAS64379.1 | |
| AY541521.1 | AAS64381.1 | |||
| AY541522.1 | AAS64382.1 | |||
| AY541523.1 | AAS64383.1 | |||
| AY541524.1 | 4 | 753 | AAS64384.1 | |
| BC032778.1 | 3 | 914 | AAH32778.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv470980 | Chr.10:133186655 - 133409514 on Build GRCh38 | Loss |
 PAOX
VENTX
MIR202
MTG1
CALY
ECHS1
ZNF511
UTF1
ADAM8
MIR3944
FUOM
MIR202HG
KNDC1
PRAP1
TUBGCP2
|
| esv2759793 | Chr.10:133030918 - 133619181 on Build GRCh38 | Gain+Loss |
PAOX
VENTX
SPRN
MIR202
MTG1
CALY
ECHS1
ZNF511
ADGRA1-AS1
UTF1
ADGRA1
ADAM8
SYCE1
MIR3944
SCART1
FUOM
MIR202HG
KNDC1
CYP2E1
PRAP1
TUBGCP2
SPRNP1
|
| nsv952707 | Chr.10:133333097 - 133403896 on Build GRCh38 | Deletion |
PAOX
FUOM
MTG1
CALY
ECHS1
PRAP1
MIR3944
|
| nsv467509 | Chr.10:133328068 - 133402966 on Build GRCh38 | Loss |
PAOX
FUOM
MTG1
CALY
ECHS1
PRAP1
MIR3944
|
| nsv428243 | Chr.10:133245214 - 133767422 on Build GRCh38 | Gain |
PAOX
SPRN
MIR202
MTG1
CALY
ECHS1
ZNF511
ADAM8
FRG2B
SYCE1
MIR3944
SCART1
FUOM
MIR202HG
CYP2E1
PRAP1
TUBGCP2
SPRNP1
|
| nsv470981 | Chr.10:133365107 - 133620799 on Build GRCh38 | Gain |
PAOX
SPRN
MTG1
ECHS1
CYP2E1
SYCE1
SPRNP1
MIR3944
SCART1
|
| dgv2e196 | Chr.10:133189913 - 133450541 on Build GRCh38 | Duplication |
PAOX
VENTX
SPRN
MIR202
MTG1
CALY
ECHS1
ZNF511
UTF1
ADAM8
MIR3944
FUOM
MIR202HG
KNDC1
PRAP1
TUBGCP2
|
| dgv35e55 | Chr.10:133370615 - 133621047 on Build GRCh38 | Gain |
PAOX
SPRN
MTG1
ECHS1
CYP2E1
SYCE1
SPRNP1
MIR3944
SCART1
|
| nsv1052904 | Chr.10:133298340 - 133769367 on Build GRCh38 | Gain |
PAOX
SPRN
MTG1
CALY
ECHS1
ZNF511
FRG2B
SYCE1
MIR3944
SCART1
FUOM
CYP2E1
PRAP1
TUBGCP2
SPRNP1
|
| nsv1037772 | Chr.10:133263092 - 133403671 on Build GRCh38 | Gain |
PAOX
FUOM
MTG1
CALY
ECHS1
ZNF511
PRAP1
ADAM8
TUBGCP2
MIR3944
|
| nsv527785 | Chr.10:133344451 - 133402966 on Build GRCh38 | Loss |
PAOX
FUOM
MTG1
ECHS1
PRAP1
MIR3944
|
| esv2750853 | Chr.10:133266358 - 133621047 on Build GRCh38 | Gain |
PAOX
SPRN
MTG1
CALY
ECHS1
ZNF511
ADAM8
SYCE1
MIR3944
SCART1
FUOM
CYP2E1
PRAP1
TUBGCP2
SPRNP1
|
| nsv528260 | Chr.10:132859348 - 133620799 on Build GRCh38 | Loss |
PAOX
MIR202
ADGRA1-AS1
UTF1
MIR3944
LINC01167
FUOM
LINC01166
MIR202HG
CFAP46
VENTX
SPRN
MTG1
CALY
ECHS1
ZNF511
ADGRA1
ADAM8
SYCE1
SCART1
LINC01168
KNDC1
CYP2E1
PRAP1
TUBGCP2
SPRNP1
|
| dgv3e196 | Chr.10:133266297 - 133450541 on Build GRCh38 | Duplication |
PAOX
SPRN
FUOM
MTG1
CALY
ECHS1
ZNF511
PRAP1
ADAM8
TUBGCP2
MIR3944
|
| nsv832040 | Chr.10:133301560 - 133412641 on Build GRCh38 | Loss |
PAOX
FUOM
MTG1
CALY
ECHS1
ZNF511
PRAP1
TUBGCP2
MIR3944
|
| nsv552589 | Chr.10:133257500 - 133563944 on Build GRCh38 | Gain |
PAOX
SPRN
MTG1
CALY
ECHS1
ZNF511
ADAM8
SYCE1
MIR3944
SCART1
FUOM
CYP2E1
PRAP1
TUBGCP2
|
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Additional Information:
For this assay, SNP(s) [rs78367010] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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