Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4731 to 4740 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4731
Flotillin 1
-
Obstructive pulmonary disease, Dental caries, Hypothyroidism, Major depressive disorder, Psoriasis, Rheumatoid arthritis, Schizophrenia, Upper aerodigestive tract neoplasm

4732
Fibronectin leucine rich transmembrane protein 1
SPG68
Gout, Hyperuricemia, Metabolic syndrome, Peripheral neuropathy, Schizophrenia, Hereditary spastic paraplegia, Diabetes mellitus type 2

4733
Fibronectin leucine rich transmembrane protein 2
-
Alzheimer disease, Cataract

4734
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

4735
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)

4736
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)

4737
Fms related receptor tyrosine kinase 3 ligand
FL, FLG3L, FLT3L, IMD125
Central nervous system cancer, Glioblastoma, Glioma, Immunodeficiency

4738
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

4739
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

4740
FLVCR choline and putative heme transporter 2
C14orf58, CCT, EPV, FLVCRL14q, MFSD7C, PVHH, SLC49A2
Byzanthine arch palate, Contracture of multiple joints, Encephaloclastic proliferative vasculopathy, Hydrops fetalis, Posterior column ataxia with retinitis pigmentosa, Ventricular septal defect