Table 5.
Disease/Disorder | Gene 1 | Gene 2 | Pseudogene? | Papers |
---|---|---|---|---|
Hereditary Neuropathy with liability to Pressure Palsies | N/A | N/A | N/A | 2 |
Charcot-Marie-Tooth disease type 1A | N/A | N/A | N/A | 3 |
Polycistic Kidney Disease | PKD1 | N/A | Yes | 3 |
Autosomal dominant facioscapulohumeral muscular dystrophy | N/A | N/A | N/A | 2 |
Breast Cancer | BRCA1 | BRCA2 | No | 1 |
Hereditary Pancreatitis | PRSS1 | R122H | No | 5 |
non-Hodgkin's Lymphoma | D6S347 | N/A | N/A | 1 |
Spinocerebellar ataxia type 8 | N/A | N/A | N/A | 2 |
Neural Tube Defects | N/A | N/A | Yes | 1 |
Friedreich's ataxia | N/A | N/A | N/A | 1 |
Pseudoxanthoma elasticum | ABCC6 | psiABCC6 | Yes (psiABCC6) | 1 |
Incontinentia pigmenti | NEMO/LAGE2 | N/A | N/A | 1 |
Schwachman Diamond Syndrome | SBDS | SBDSP | Yes (SBDSP) | 6 |
Hypergonadotrophic Hypogonadism | FSHR | N/A | N/A | 1 |
Smith-Magenis Syndrome | N/A | N/A | N/A | 1 |
Human Male Infertility | DAZ genes | N/A | N/A | 2 |
Hemophilia A | F8 | N/A | N/A | 1 |
Chronic Pancreatitis | PRSS1 | PRSS2 | No | 1 |
Campomelic dysplasia | SOX9 | N/A | N/A | 1 |
Machado-Joseph Disease | MJD/SCA3 | N/A | N/A | 2 |
Sodium-sensitive cardiac hypertrophy | CYPB112 | N/A | N/A | 1 |
Obesity | HTR2C | N/A | N/A | 1 |
Velo-cardio-facial syndrome/DiGeorge syndrome | LCR22-2 | LCR22-4 | No | 1 |
Hereditary Nonpolyposis Colorectal Cancer | MLH1 | MSH2 | No | 1 |
Atypical Hemolytic Uremic Syndrome | CFH | CFH1 | No | 1 |
Pyridoxine-responsive Homocystinuria | CBS | N/A | N/A | 1 |
Autosomal Dominant Cataract | CRYBB2 | CRYBB2P1 | Yes (CRYBB2P1) | 1 |
In this table we list the diseases and disorders associated with gene conversions. In addition, we list the genes involved where applicable (listed here as Gene 1 and Gene 2) as well as whether one was a pseudogene (and listing which is if this information was available). Finally, we list the number of abstracts that dealt with the disease/disorder.