|
| AFFYMETRIX_3PRIME_IVT_ID | Gene name | Disease caused |
|
| 200620_at | Transmembrane protein 59 | Alzheimer’s disease |
| 200877_at | Chaperonin containing TCP1, subunit 4 (delta) | Hereditary sensory neuropathy |
| 201393_s_at | Insulin-like growth factor 2 receptor | Parkinson’s disease |
| 201586_s_at | Splicing factor proline/glutamine-rich (polypyrimidine tract-binding protein associated) | Papillary renal cell carcinoma |
| 201619_at | Peroxiredoxin 3 | Oxidative stress to cells—Alzheimer’sand Parkinson’s disease |
| 201823_s_at | Ring finger protein 14 | Insulin Resistance Syndrome |
| 202438_x_at | Iduronate 2-sulfatase | Hunter syndrome |
| 202591_s_at | Single-stranded DNA-binding protein 1 | Crown gall disease |
| 202761_s_at | Spectrin repeat containing, nuclear envelope 2 | Cerebellar ataxia type 1 |
| 202836_s_at | Thioredoxin-like 4A | Niemann-Pick disease |
| 203310_at | Syntaxin-binding protein 3 | Cardiovascular disease |
| 203874_s_at | SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily a, member 1 | Autosomal recessive pleiotropic disorder |
| 204063_s_at | unc-51-like kinase 2 (C. elegans) | Polycystic kidney disease |
| 204500_s_at | ATP/GTP-binding protein 1 | Musculoskeletal disease |
| 205029_s_at | Fatty-acid-binding protein 7, brain | Coronary disease |
| 205626_s_at | Calbindin 1, 28 kDa | Parkinson’s disease |
| 207168_s_at | H2A histone family, member Y | Ataxia-Telangiectasia |
| 208684_at | coatomer protein complex, subunit alpha | Protein energy malnutrition |
| 208742_s_at | Sin3A-associated protein, 18 kDa | Huntington’s disease |
| 208758_at | 5-Aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Non-Hodgkin’s lymphoma |
| 209025_s_at | Synaptotagmin-binding, cytoplasmic RNA-interacting protein | Alzheimer’s disease |
|
