851
|
|
|
Fin bud initiation factor homolog |
- |
Curated: Dental caries, Heart failure, Otosclerosis
Unreviewed: Heart Failure, Mental Disorders
|
852
|
|
|
FGF1 intracellular binding protein |
FGFIBP, FIBP-1, TROFAS |
Curated: Alzheimer disease, Ankylosing spondylitis, Congenital facial anomaly, Congenital ocular coloboma, Crohn disease, Gastroesophageal reflux disease, Inflammatory bowel disease, Learning disorders, Psoriasis, Sclerosing cholangitis, Thauvin-robinet-faivre syndrome, Ulcerative colitis
Unreviewed: Ankylosing Spondylitis, Aortic aneurysm, Breast neoplasm, Cholangitis, Colorectal Cancer, Congenital Epicanthus, Crohn Disease, Developmental Delay, Facial dysmorphism, Learning Disorders, Liver Cirrhosis, Lung neoplasms, Macroglossia, Macrotia, Malrotation Of Kidney, Mental retardation, Mitral Valve Prolapse, Nephroblastoma, Renal dysplasia, Strabismus, Thauvin-Robinet-Faivre Syndrome, Vulval varices
|
853
|
|
|
FIC domain protein adenylyltransferase |
HIP13, HYPE, SPG92, UNQ3041 |
Curated: Spastic paraplegia
Unreviewed: Motor neuron disease, Neurodegenerative disorder
|
854
|
|
|
FIG4 phosphoinositide 5-phosphatase |
ALS11, BOP, BTOP, CMT4J, KIAA0274, SAC3, YVS, dJ249I4.1 |
Curated: Amyotrophic lateral sclerosis, Distal hereditary motor neuropathy, Bilateral parasagittal parieto-occipital polymicrogyria, Charcot-marie-tooth disease, Dejerine-sottas disease, Desbuquois syndrome, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Major depressive disorder, Micropenis, Penile hypospadia, Peroneal muscle atrophy, Polymicrogyria, Roussy-levy syndrome, Diabetes mellitus type 2, Yunis-varon syndrome, amyotrophic lateral sclerosis type 11
Unreviewed: Agenesis Of Corpus Callosum, Alzheimer disease, Amyotrophic Lateral Sclerosis, Androgen insensitivity syndrome, Anxiety Disorder, Arrhinencephaly, Arthritis, Atrial Septal Defect, Bilateral Occipital Polymicrogyria, Bilateral Parasagittal Parieto-Occipital Polymicrogyria, Breast Cancer, Breast Carcinoma, Cardiomyopathy, Cataract, Central nervous system disease, Cerebellar Hypoplasia, Charcot-Marie-Tooth Disease, Congenital Absent Nipple, Congenital Anomaly Of Neck, Congenital Microcephaly, Cryptorchidism, Defect Of Skull Ossification, Delirium, Demyelinating Diseases, Demyelinating neuropathy, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Distal arthrogryposis, Dolichocephaly, Dwarfism, Dysautonomia, Dyscognitive seizures, Epilepsy, Frontotemporal dementia, Gaucher disease, Gingival Recession, Glioma, Glossoptosis, Glycogen storage disease, Hereditary motor and sensory neuropathy, Hereditary spastic paraplegia, Huntington disease, Hydrocephalus, Hydrops Fetalis, Hypertension, Hypertrophy Of Clitoris, Hypopigmentation Disorder, Hypospadias, Laryngospasm, Lateral Sclerosis, Leukoencephalopathy, Mental Depression, Metachromatic leukodystrophy, Microcephaly, MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES, Micrognathism, Microphthalmos, Mood swings, Motor neuron atrophy, Motor Neuron Disease, Nervous system disease, Nervous System Diseases, Neuroblastoma, Neurodegenerative Disorders, Neuropathy, Pachygyria, Papillon-Lefevre Disease, Paralysis, Parkinson disease, Penis Agenesis, Peripheral nervous system disease, Peripheral Neuropathy, Proptosis, Pulmonary arterial hypertension, Renal Artery Stenosis, Renal cell carcinoma, Respiratory Failure, Roussy-Levy Syndrome, Sclerocornea, Secondary parkinson disease, Seizure, Seizures, Short clavicles, Spastic Paraplegia, Status Epilepticus, Syndactyly, Syndactyly Of The Toes, Tetralogy of Fallot, Thumb Aplasia, Triple Negative Breast Neoplasms, Ventricular septal defect, Vertical Talus, Yunis Varon Syndrome
|
855
|
|
|
Folliculogenesis specific bHLH transcription factor |
BHLHC8, FIGALPHA, POF6 |
Curated: Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Gonadal dysgenesis, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Ovarian cancer, Premature ovarian failure, Ovarian serous carcinoma, Pancreatic cancer, Prostate cancer, Squamous cell carcinoma
Unreviewed: Dwarfism, Ovarian Failure, Physiologic Amenorrhea, Premature Menopause, Premature Ovarian Failure, Secondary Physiologic Amenorrhea, Sezary syndrome
|
856
|
|
|
FIGLA pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
857
|
|
|
Fidgetin, microtubule severing factor |
- |
Curated: Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Cardiovascular disease, Kidney disease, Coronary artery disease, Cystitis, Developmental disability, Hypertension, Henoch schoenlein purpura, Myocardial infarction, Polycystic ovary syndrome, Willis-ekbom disease, Substance abuse
Unreviewed: Congenital Heart Disease, Coronary Heart Disease, Hepatocellular carcinoma, Thrombosis
|
858
|
|
|
Fidgetin like 1 |
- |
Curated: Kidney neoplasms
Unreviewed: Deficiency Of Aromatic-L-Amino-Acid Decarboxylase, Dysarthria, Kidney Cancer, Kidney Neoplasm, Lung carcinoma, Lymphoblastic Leukemia, Macular degeneration, Mental retardation, Small cell lung carcinoma
|
859
|
|
|
Fidgetin like 2 |
- |
Curated: N/A
Unreviewed: N/A
|
860
|
|
|
FIGNL2 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|