391
|
|
|
FLII actin remodeling protein |
CMD2J, FLI, FLIL, Fli1 |
|
392
|
|
|
Filamin A |
ABP-280, ABPX, CSBS, CVD1, FGS2, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD |
Ambiguous genitalia, Aortic aneurysm, Breast neoplasms, Cardiac valvular dysplasia, Conductive hearing loss, Congenital cartilage disorder, Congenital heart defects, Congenital idiopathic intestinal pseudoobstruction, Congenital omphalocele, Congenital short bowel syndrome, Connective tissue disease, Craniosynostosis, Desbuquois syndrome, Developmental delay, Dysgenesis of corpus callosum, Developmental and epileptic encephalopathy, Ehlers-danlos syndrome, Epilepsy, Thoracic aortic aneurysm and aortic dissection, Frontometaphyseal dysplasia, Global developmental delay, Hearing impairment, Periventricular nodular heterotopia, Hydronephrosis, Intellectual developmental disorder, Intestinal obstruction, Liver cirrhosis, Marfan syndrome, Migraine, Mitral valve prolapse, Myopia, Neurodevelopmental disorder, Nonalcoholic fatty liver disease, Orofacial cleft, Osteochondrodysplasias, Otopalatodigital spectrum disorder, Otopalatodigital syndrome, Patent ductus arteriosus, Periventricular heterotopia, x-linked, Scoliosis, Intellectual disability, Terminal osseous dysplasia with pigmentary defects, Tetralogy of fallot, Thrombocytopenia, Uranostaphyloschisis, Ventricular septal defect, Wolff-parkinson-white syndrome, X-linked ehlers-danlos syndrome, X-linked keloid scarring syndromeView all (34 more) |
393
|
|
|
Filamin B |
ABP-278, ABP-280, AOI, FH1, FLN-B, FLN1L, LRS1, SCT, TABP, TAP |
Alzheimer disease, Aortic stenosis, Aortic valve disease, Atelosteogenesis, Boomerang dysplasia, Breast cancer, Bullous pemphigoid, Cleft palate, Congenital cartilage disorder, Congenital clubfoot, Connective tissue disease, Desbuquois syndrome, Digestive system disease, Eating disorder, Glaucoma, Larsen syndrome, Open angle glaucoma, Osteochondrodysplasias, Systemic sclerosisView all (4 more) |
394
|
|
|
Filamin C |
ABP-280, ABP280A, ABPA, ABPL, ARVC15, CMH26, FLN2, MFM5, MPD4, RCM5 |
Cardiac arrhythmias, Arrhythmogenic right ventricular cardiomyopathy, Asymmetric septal hypertrophy, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular disease, Cerebellar ataxia, Colorectal neoplasms, Conduction disorder of the heart, Distal myopathy, Restrictive cardiomyopathy, Heart disease, Heart failure, Hypertrophic cardiomyopathy, Myofibrillar myopathy, Nemaline myopathy, Spastic ataxia, Tetralogy of fallot, Wolff-parkinson-white syndromeView all (4 more) |
395
|
|
|
Flotillin 1 |
- |
|
396
|
|
|
Fibronectin leucine rich transmembrane protein 1 |
SPG68 |
|
397
|
|
|
Fibronectin leucine rich transmembrane protein 2 |
- |
|
398
|
|
|
Fibronectin leucine rich transmembrane protein 3 |
HH21 |
|
399
|
|
|
Fms related receptor tyrosine kinase 1 |
FLT, FLT-1, VEGFR-1, VEGFR1 |
Autism, Breast cancer, Breast neoplasms, Bronchopulmonary dysplasia, Renal cell carcinoma, Cerebral hemorrhage, Obstructive pulmonary disease, Congenital cartilage disorder, Coronary artery disease, Diabetic retinopathy, Age-related macular degeneration, Hemangiosarcoma, Large artery stroke, Liver cirrhosis, Melanoma, Moyamoya disease, Myocardial infarction, Osteochondrodysplasias, Preeclampsia, Scoliosis, Skin neoplasms, UremiaView all (7 more) |
400
|
|
|
Fms related receptor tyrosine kinase 3 |
CD135, FLK-2, FLK2, STK1 |
Autoimmune disease, Autoimmune thyroid disease, B-cell acute lymphoblastic leukemia, B-lymphoblastic leukemia/lymphoma, Duodenal ulcer, Hypothyroidism, Lymphoblastic leukemia, Myeloid leukemia, Promyelocytic leukemia, Metabolic syndrome, Psoriasis, Rheumatoid arthritis, Splenomegaly, Thrombosis, Tourette syndrome, Diabetes mellitus type 2View all (1 more) |
