Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4701 to 4710 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4701
FH2 domain containing 1
INF1
Amyotrophic lateral sclerosis, Obesity, Oligodendroglioma, Thyrotoxic periodic paralysis

4702
FHF complex subunit HOOK interacting protein 1A
FAM160A1, FHIP-L
Attention deficit hyperactivity disorder, Autism, Dyslexia, Insomnia, Intracerebral hemorrhage, Myopia

4703
FHF complex subunit HOOK interacting protein 2A
FAM160B1, KIAA1600, bA106M7.3
Alzheimer disease, Melanoma

4704
FHF complex subunit HOOK interacting protein 2B
FAI16, FAM160B2, RAI16, RAM160B2
Cholecystitis, Cholecystolithiasis, Melanoma, Metabolic syndrome, Diabetes mellitus type 2

4705
Fragile histidine triad diadenosine triphosphatase
AP3Aase, FRA3B
Amphetamine or sympathomimetic abuse, Anorexia nervosa, Asperger syndrome, Astrocytoma, Atrioventricular block, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brain aneurysm, Bronchopulmonary dysplasia, Carcinoma, Non-small-cell lung carcinoma, Color vision deficiency, Colorectal cancer, Dementia
View all (28 more)

4706
Four and a half LIM domains 1
FCMSU, FHL-1, FHL1A, FHL1B, FLH1A, KYOT, RBMX1A, RBMX1B, SLIM, SLIM-1, SLIM1, SLIMMER, XMPMA
Asymmetric septal hypertrophy, Cardiomyopathy, Centronuclear myopathy, Emery-dreifuss muscular dystrophy, Heart failure, Hemophagocytic lymphohistiocytosis, Hypertrophic cardiomyopathy, Liver cirrhosis, Reducing body myopathy, Scapuloperoneal myopathy, Uruguay faciocardio-musculoskeletal syndrome, X-linked emery-dreifuss muscular dystrophy, X-linked myopathy, X-linked scapuloperoneal muscular dystrophy

4707
Four and a half LIM domains 2
AAG11, DRAL, FHL-2, SLIM-3, SLIM3
Arrhythmogenic right ventricular cardiomyopathy, Attention deficit hyperactivity disorder, Bipolar disorder, Breast neoplasms, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Central nervous system cancer, Glioblastoma, Glioma, Left ventricular noncompaction cardiomyopathy, Myeloid leukemia, Liver cirrhosis, Lung cancer, Major depressive disorder
View all (1 more)

4708
Four and a half LIM domains 3
SLIM2
Androgenetic alopecia, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Open angle glaucoma

4709
Four and a half LIM domains 5
1700027G07Rik, ACT, FHL-5, dJ393D12.2
Brain aneurysm, Coronary artery disease, Endometriosis, Migraine, Myocardial infarction

4710
Formin homology 2 domain containing 3
CMH28, FHOS2, Formactin2
Alzheimer disease, Cardiomyopathy, Dilated cardiomyopathy, Color vision deficiency, Dementia, Hypertrophic cardiomyopathy, Otosclerosis, Ovarian cancer, Periodontitis, Scoliosis, Spinal muscular atrophy