Genomic Map
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Target Gene Details
Entrez Gene ID: | 80833 |
Gene Name: | apolipoprotein L3 |
Gene Aliases: |
APOLIII, CG121, CG12_1, apoL-III |
Location: |
Chr.22:36140323-36166177 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| APOL3 | NM_014349.2 | 3 | 627 | NP_055164.1 |
| NM_030644.1 | 4 | 511 | NP_085147.1 | |
| NM_145639.1 | 3 | 398 | NP_663614.1 | |
| NM_145640.2 | 2 | 301 | NP_663615.1 | |
| NM_145641.2 | 4 | 1810 | NP_663616.1 | |
| NM_145642.2 | 3 | 1747 | NP_663617.1 | |
| XM_006724324.1 | 4 | 389 | XP_006724387.1 | |
| XM_006724325.2 | 3 | 300 | XP_006724388.1 | |
| XM_017028946.1 | 3 | 227 | XP_016884435.1 | |
| XM_017028947.1 | 4 | 340 | XP_016884436.1 | |
| XM_017028948.1 | 5 | 644 | XP_016884437.1 | |
| XM_017028949.1 | 5 | 529 | XP_016884438.1 | |
| XM_017028950.1 | 4 | 1234 | XP_016884439.1 | |
| XM_017028951.1 | 3 | 1121 | XP_016884440.1 | |
| XM_017028952.1 | 2 | 147 | XP_016884441.1 | |
| AF070675.1 | 3 | 467 | AAC83233.1 | |
| AF305227.1 | 3 | 254 | AAK20213.1 | |
| AK025349.1 | 3 | 224 | ||
| AY014902.1 | 4 | 511 | AAG50344.1 | |
| AY014903.1 | 3 | 398 | AAG50345.1 | |
| AY014904.1 | 2 | 301 | AAG50346.1 | |
| AY014905.1 | 3 | 627 | AAG50347.1 | |
| AY014906.1 | 4 | 1810 | AAG50348.1 | |
| AY014907.1 | 3 | 1747 | AAG50349.1 | |
| BC042918.1 | 3 | 203 | AAH42918.1 | |
| BC050596.1 | 3 | 258 | AAH50596.1 | |
| BF797347.1 | 2 | 162 | ||
| CR456379.1 | 2 | 121 | CAG30265.1 | |
| DA878288.1 | 2 | 231 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv8093n54 | Chr.22:36137894 - 36187036 on Build GRCh38 | Loss |
 APOL3
|
| esv2751964 | Chr.22:36137737 - 36183513 on Build GRCh38 | Loss |
APOL3
|
| dgv4563n100 | Chr.22:36142329 - 36186502 on Build GRCh38 | Loss |
APOL3
|
| esv3647677 | Chr.22:36137690 - 36164506 on Build GRCh38 | Loss |
APOL3
|
| nsv526454 | Chr.22:36143804 - 36187036 on Build GRCh38 | Loss |
APOL3
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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