Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4911 to 4920 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4911
Fucosyltransferase 3 (Lewis blood group)
CD174, FT3B, FucT-III, LE, Les
Cholecystolithiasis, Colorectal cancer, Deficiency anemia, Gallstones, Idiopathic pulmonary fibrosis, Vitamin b12 deficiency

4912
Fucosyltransferase 4
CD15, ELFT, FCT3A, FUC-TIV, FUTIV, LeX, SSEA-1
Thrombosis

4913
Fucosyltransferase 6
FCT3A, FT1A, Fuc-TVI, FucT-VI
Atrophic macular degeneration, Cholecystolithiasis, Colorectal cancer, Deficiency anemia, Gallstones, Idiopathic pulmonary fibrosis, Vitamin b deficiency, Vitamin b12 deficiency, Age-related macular degeneration

4914
Fucosyltransferase 7
FucT-VII
Polycystic ovary syndrome

4915
Fucosyltransferase 8
CDGF, CDGF1
Obstructive pulmonary disease, Congenital disorder of glycosylation, Gout, Metabolic syndrome, Multiple sclerosis, Obesity, Schizophrenia, Stroke, Diabetes mellitus type 2

4916
Fucosyltransferase 9
Fuc-TIX
Colorectal cancer, Diabetic neuropathy, Migraine, Schizophrenia

4917
Fuzzy planar cell polarity protein
CPLANE3, FY, NTD
Caudal regression syndrome, Desbuquois syndrome, Jeune thoracic dystrophy, Majewski syndrome, Neural tube defect, Neural tube defects, x-linked, Neural tube defects, susceptibility to

4918
Frataxin
CyaY, FA, FARR, FRDA, X25
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Diabetes mellitus type 2, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Lung cancer, Major depressive disorder, Migraine
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4919
FMR1 autosomal homolog 1
CMYO9A, CMYO9B, CMYP9A, CMYP9B, FXR1P, MYOPMIL, MYORIBF
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Congenital myopathy, Eating disorder, Gross motor development delay, Insomnia, Intellectual developmental disorder, Mastocytosis, Obesity, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 2

4920
FMR1 autosomal homolog 2
FMR1L2, FXR2P
Atrial fibrillation, Atrial flutter