Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "F"
171 to 180 of 433 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
FANCD2 and FANCI associated nuclease 1
KIAA1018, KMIN, MTMR15, hFAN1
Lynch syndrome, Huntington disease, Hypertriglyceridemia, Interstitial nephritis, Upper aerodigestive tract neoplasm

172
Forkhead box F1
ACDMPV, FKHL5, FREAC1
Alveolar capillary dysplasia, Congenital alveolar capillary dysplasia, Gastrointestinal stromal tumor, Pulmonary hypertension, Lung disease, Mastocytosis, Vacterl association, Ventricular septal defect

173
Forkhead box F2
FKHL6, FREAC-2, FREAC2
Androgenetic alopecia, Cerebrovascular disorder, Erectile dysfunction, Glioma, Major depressive disorder, Mood disorder, Ovarian cancer, Ovarian serous carcinoma, Stroke, Urinary bladder cancer

174
Forkhead box C1
ARA, ASGD3, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1, RIEG3
Aniridia, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Spinocerebellar ataxia, Axenfeld anomaly, Axenfeld-rieger syndrome, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Coronary artery disease, Dandy-walker syndrome, Hypertension, Glaucoma, Iridogoniodysgenesis, Myocardial infarction, Prostatic neoplasm
View all (1 more)

175
Forkhead box I1
FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3
Distal renal tubular acidosis, Nonsyndromic hearing loss, Breast cancer, Craniofacial abnormalities, Deafness, Hearing impairment, Pendred syndrome, Triple-negative breast cancer

176
Forkhead box E3
AAT11, ASGD2, CATC3, CTRCT34, FKHL12, FREAC8
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Aortic aneurysm, Congenital primary aphakia, Cataract, Congenital cataract, Congenital aneurysm of ascending aorta, Congenital aphakia, Thoracic aortic aneurysm and aortic dissection, Retinitis pigmentosa

177
F-box protein 21
FBX21
Astrocytoma, Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Insomnia, Metabolic syndrome, Diabetes mellitus, type 2

178
Fas apoptotic inhibitory molecule 2
LFG, LFG2, NGP35, NMP35, TMBIM2
Diabetes mellitus, Gout, Hyperpituitarism, Obesity, Diabetes mellitus, type 2

179
Forkhead box J1
CILD43, FKHL13, HFH-4, HFH4
Ciliary dyskinesia

180
Forkhead box C2
FKHL14, LD, MFH-1, MFH1
Blepharoptosis, Cardiovascular disease, Craniofacial abnormalities, Diabetes mellitus type 2, Distichiasis-lymphedema syndrome, Eyelid disease, Non-immune hydrops fetalis, Hypertension, Lymphedema, Obesity