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
4891 to 4900 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4891
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

4892
Fucosyltransferase 7
FucT-VII
Polycystic ovary syndrome

4893
Fucosyltransferase 8
CDGF, CDGF1
Obstructive pulmonary disease, Congenital disorder of glycosylation, Gout, Metabolic syndrome, Multiple sclerosis, Obesity, Schizophrenia, Stroke, Diabetes mellitus type 2

4894
Fucosyltransferase 9
Fuc-TIX
Colorectal cancer, Diabetic neuropathy, Migraine, Schizophrenia

4895
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

4896
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
View all (8 more)

4897
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

4898
FMR1 autosomal homolog 2
FMR1L2, FXR2P
Atrial fibrillation, Atrial flutter

4899
FXYD domain containing ion transport regulator 1
PLM
Schizophrenia

4900
FXYD domain containing ion transport regulator 2
ATP1G1, HOMG2
Primary hypomagnesemia with hypocalciuria, Magnesium metabolism disorder, Hyperopia, Hypertension, Diabetes mellitus type 2