391
|
|
|
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) |
392
|
|
|
Flotillin 1 |
- |
|
393
|
|
|
Fibronectin leucine rich transmembrane protein 1 |
SPG68 |
|
394
|
|
|
Fibronectin leucine rich transmembrane protein 2 |
- |
|
395
|
|
|
Fibronectin leucine rich transmembrane protein 3 |
HH21 |
|
396
|
|
|
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) |
397
|
|
|
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) |
398
|
|
|
Fms related receptor tyrosine kinase 3 ligand |
FL, FLG3L, FLT3L, IMD125 |
|
399
|
|
|
Fms related receptor tyrosine kinase 4 |
CHTD7, FLT-4, FLT41, LMPH1A, LMPHM1, PCL, VEGFR-3, VEGFR3 |
|
400
|
|
|
FLVCR choline and heme transporter 1 |
AXPC1, FLVCR, MFSD7B, NEDMISH, PCA, PCARP, RETSNS, SLC49A1 |
Asthma, Hepatocellular carcinoma, Hereditary sensory and autonomic neuropathy, Jeune thoracic dystrophy, Neurodevelopmental disorder, Posterior column ataxia with retinitis pigmentosa, Retinitis pigmentosa, Retinopathy-sensory neuropathy syndrome, Sensory neuropathy, Short rib dysplasia-polydactyly syndrome, Stargardt disease |