|
301
|
|
|
Cdc42 guanine nucleotide exchange factor 9 |
COLLYBISTIN, DEE8, EIEE8, HPEM-2, PEM-2, PEM2 |
Androgenetic alopecia, Autism, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Hyperekplexia epilepsy syndrome, Hypogonadism, Intellectual developmental disorder, X-linked complex neurodevelopmental disorder, X-linked intellectual disability |
|
302
|
|
|
Activity regulated cytoskeleton associated protein |
Arg3.1, hArc |
|
|
303
|
|
|
Astrotactin 2 |
bA67K19.1 |
Amphetamine or related acting sympathomimetic abuse, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Colon cancer, Common migraine, Coronary artery disease, Cystitis, Endometriosis, Estrogen-receptor negative breast cancer, Hearing loss, Hemorrhoid, Osteonecrosis of the femoral head, Insomnia, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Obesity, Myopathy, Neurotic disorder, Osteoarthritis, Pancreatic cancer, Willis-ekbom disease, Rotator cuff tear, Schizophrenia, Scoliosis, Diabetes mellitus, type 2, Uterine polyp, Venous thromboembolismView all (21 more) |
|
304
|
|
|
ATPase phospholipid transporting 11A |
ATPIH, ATPIS, AUNA2, DFNA84, HLD24 |
Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Basal cell carcinoma, Neurodevelopmental disorder, Melanoma, Deafness, Hearing loss, Hypomyelinating leukodystrophy, Idiopathic pulmonary fibrosis, Interstitial lung disease, Keratinocyte carcinoma, Machado-joseph disease, Non-specific syndromic intellectual disability, Severe acute respiratory syndrome, Skin cancer, Skin neoplasm, Squamous cell carcinoma, Ventricular fibrillationView all (4 more) |
|
305
|
|
|
Adhesion G protein-coupled receptor L2 |
CIRL2, CL2, LEC1, LPHH1, LPHN2 |
Alzheimer disease, Ankylosing spondylitis, Attention deficit hyperactivity disorder, Autoimmune disease, Autoimmune thyroid disease, Bladder exstrophy, Breast cancer, Cataract, Celiac disease, Color vision deficiency, Common variable immunodeficiency, Coronary artery disease, Crohn disease, Dental caries, Diabetic neuropathy, Dyslexia, Gastroesophageal reflux disease, Glomerulonephritis, Gout, Juvenile idiopathic arthritis, Metabolic syndrome, Myocardial infarction, Obesity, Ovarian cancer, Prostate cancer, Psoriasis, Schizophrenia, Scoliosis, Secondary malignant neoplasm, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitis, Upper aerodigestive tract neoplasm, Venous thromboembolismView all (21 more) |
|
306
|
|
|
Adhesion G protein-coupled receptor L3 |
CIRL3, CL3, LEC3, LPHN3 |
Attention deficit hyperactivity disorder, Central nervous system cancer, Kidney disease, Coronary artery disease, Eosinophilia, Epilepsy, Generalized epilepsy, Glioma, Insomnia, Myocardial infarction, Open angle glaucoma, Partial epilepsy, Schizophrenia, Severe acute respiratory syndrome, Stroke, Substance abuseView all (1 more) |
|
307
|
|
|
ATP/GTP binding carboxypeptidase 1 |
CCP1, CONDCA, NNA1 |
|
|
308
|
|
|
Ankyrin repeat and sterile alpha motif domain containing 1A |
ANKS1 |
Ischemic heart disease, Rhinosinusitis, Coronary artery disease, Graves disease, Metabolic syndrome, Myocardial ischemia, Non-small cell lung carcinoma, Obesity, Psoriasis, Sinusitis, Systemic lupus erythematosus, Systemic sclerosis, Diabetes mellitus, type 2 |
|
309
|
|
|
Acyl-CoA synthetase long chain family member 6 |
ACS2, FACL6, LACS 6, LACS2, LACS5 |
|
|
310
|
|
|
ALF transcription elongation factor 2 |
FMR2, FMR2P, FRAXE, MRX2, OX19, XLID109 |
Colon cancer, Colorectal cancer, Congenital microcephaly, Aplastic anemia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Kidney disease, Myopia, Neurotic disorder, X-linked intellectual disability, Premature ovarian failure, Scoliosis |
