Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
4751 to 4760 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4751
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
View all (4 more)

4752
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
View all (4 more)

4753
Flotillin 1
-
Obstructive pulmonary disease, Dental caries, Hypothyroidism, Major depressive disorder, Psoriasis, Rheumatoid arthritis, Schizophrenia, Upper aerodigestive tract neoplasm

4754
Fibronectin leucine rich transmembrane protein 1
SPG68
Gout, Hyperuricemia, Metabolic syndrome, Peripheral neuropathy, Schizophrenia, Hereditary spastic paraplegia, Diabetes mellitus type 2

4755
Fibronectin leucine rich transmembrane protein 2
-
Alzheimer disease, Cataract

4756
Fibronectin leucine rich transmembrane protein 3
HH21
Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Mood disorder, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Myopia, Sheehan syndrome

4757
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
View all (7 more)

4758
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
View all (1 more)

4759
Fms related receptor tyrosine kinase 3 ligand
FL, FLG3L, FLT3L, IMD125
Central nervous system cancer, Glioblastoma, Glioma, Immunodeficiency

4760
Fms related receptor tyrosine kinase 4
CHTD7, FLT-4, FLT41, LMPH1A, LMPHM1, PCL, VEGFR-3, VEGFR3
Capillary infantile hemangioma, Renal cell carcinoma, Congenital heart disease, Dementia, Non-immune hydrops fetalis, Lymphatic malformation, Lymphedema, Polycystic ovary syndrome, Tetralogy of fallot