4511
|
|
|
Family with sequence similarity 91 member A1 |
- |
|
4512
|
|
|
Family with sequence similarity 98 member A |
- |
|
4513
|
|
|
Family with sequence similarity 98 member B |
- |
|
4514
|
|
|
Family with sequence similarity 98 member C |
- |
|
4515
|
|
|
Family with sequence similarity 9 member B |
TEX39B |
|
4516
|
|
|
Family with sequence similarity 9 member C |
TEX39C |
|
4517
|
|
|
FANCD2 and FANCI associated nuclease 1 |
KIAA1018, KMIN, MTMR15, hFAN1 |
|
4518
|
|
|
FA complementation group A |
FA, FA-H, FA1, FAA, FACA, FAH, FANCH |
Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Adenoid cystic carcinoma, Cervical cancer, Colorectal cancer, Melanoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Fanconi anemia, Gastric cancer, Hepatocellular carcinoma, Hyperinsulinism, Keratinocyte carcinoma, Lung cancer, Renal pelvis neoplasms, Neurodevelopmental disorder, Non-hodgkins lymphoma, Non-melanoma skin carcinoma, Open angle glaucoma, Ovarian cancer, Premature ovarian failure, Ovarian serous carcinoma, Pancreatic cancer, Pituitary stalk interruption syndrome, Prostate cancer, Salivary gland neoplasms, Schizophrenia, Squamous cell carcinoma, Stroke, Urinary bladder neoplasms, VitiligoView all (19 more) |
4519
|
|
|
FA complementation group B |
FA2, FAAP90, FAAP95, FAB, FACB |
|
4520
|
|
|
FA complementation group C |
FA3, FAC, FACC |
Atrial fibrillation, Color vision deficiency, Colorectal cancer, Congenital cardiovascular anomaly, Esophageal squamous cell carcinoma, Fanconi anemia, Hyperinsulinism, Dermatomyositis, Pancreatic neoplasms, Neurotic disorder, Ovarian cancer, Premature ovarian failure, Pancytopenia, Peripheral vascular disease, Prostate cancer, Diabetes mellitus type 2View all (1 more) |