Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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

Showing genes starting with "A"

951 to 960 of 1165 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
951	51130	ASB3	Ankyrin repeat and SOCS box containing 3	ASB-3	Alzheimer disease, Anorexia nervosa, Anti-neutrophil antibody associated vasculitis, Bulimia, Color vision deficiency, Dementia, Eating disorder, Gastric cancer, Gastroesophageal reflux disease, Generalized anxiety disorder, Insomnia, Lung cancer, Major depressive disorder, Metabolic syndrome, Obesity View all (7 more)
952	51666	ASB4	Ankyrin repeat and SOCS box containing 4	ASB-4	Irritable bowel syndrome, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer
953	140460	ASB7	Ankyrin repeat and SOCS box containing 7	-	Androgenetic alopecia, Glaucoma, Oligodendroglioma, Open angle glaucoma
954	51008	ASCC1	Activating signal cointegrator 1 complex subunit 1	ASC1p50, CGI-18, SMABF2, p50	Alzheimer disease, Arthrogryposis multiplex congenita, Barrett esophagus, Centronuclear myopathy, Dementia, Endometriosis, Major depressive disorder, Migraine, Pena-shokeir syndrome , Sarcoidosis, Spinal muscular atrophy, Hypertension
955	84164	ASCC2	Activating signal cointegrator 1 complex subunit 2	ASC1p100, p100	Alzheimer disease, Aortic stenosis, Aortic valve disease, Attention deficit hyperactivity disorder, Bipolar disorder, Obstructive pulmonary disease, Dental caries, Inflammatory bowel disease, Irritable bowel syndrome, Migraine, Scoliosis, Diabetes mellitus type 2
956	10973	ASCC3	Activating signal cointegrator 1 complex subunit 3	ASC1p200, HELIC1, MRT81, RNAH	Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Bipolar disorder, Congenital myopathy, Insomnia, Intellectual developmental disorder, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Nephrolithiasis, Neurotic disorder, Post-traumatic stress disorder, Substance abuse, Diabetes mellitus type 2
957	429	ASCL1	Achaete-scute family bHLH transcription factor 1	ASH1, HASH1, MASH1, bHLHa46	Haddad syndrome, Congenital central hypoventilation syndrome, Intellectual developmental disorder, Major depressive disorder, Nervous system disease, Neurodevelopmental disorder, Neurotic disorder, Oligodendroglioma, Ovarian cancer, Ovarian serous carcinoma, Schizophrenia, Small cell lung carcinoma
958	430	ASCL2	Achaete-scute family bHLH transcription factor 2	ASH2, HASH2, MASH2, bHLHa45	Ankylosing spondylitis, Lymphocytic leukemia, Colonic neoplasms, Crohn disease, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Inflammatory bowel disease, Metabolic syndrome, Obesity, Orofacial cleft, Prostate cancer, Psoriasis, Sarcoidosis View all (5 more)
959	56676	ASCL3	Achaete-scute family bHLH transcription factor 3	HASH3, SGN1, bHLHa42	Otosclerosis
960	121549	ASCL4	Achaete-scute family bHLH transcription factor 4	ASH-4, HASH4, bHLHa44	Attention deficit hyperactivity disorder, Color vision deficiency, Lung cancer, Metabolic syndrome, Parkinson disease, Pelvic organ prolapse, Prostate cancer, Squamous cell carcinoma, Substance abuse, Diabetes mellitus type 2

«««...94 959697 98...»»»