Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

301 to 310 of 912 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
301	23229	ARHGEF9	Cdc42 guanine nucleotide exchange factor 9	COLLYBISTIN, DEE8, EIEE8, HPEM-2, PEM-2, PEM2	Alopecia, Developmental regression, Dyscognitive seizures, Epileptic encephalopathy, Hyperekplexia-epilepsy syndrome, Mental retardation, Seizure, Trigonocephaly
302	23237	ARC	Activity regulated cytoskeleton associated protein	Arg3.1, hArc	Alzheimer disease, Movement disorders, Schizophrenia, Senile dementia, Status marmoratus
303	23245	ASTN2	Astrotactin 2	bA67K19.1	Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Bipolar disorder, Breast cancer, Breast carcinoma, Chronic obstructive pulmonary disease, Colorectal neoplasms, Common migraine, Depressed bipolar disorder, Limb-girdle muscular dystrophy, Mental depression, Migraine, Myopathy, Osteoarthritis of hip View all (3 more)
304	23250	ATP11A	ATPase phospholipid transporting 11A	ATPIH, ATPIS, AUNA2, DFNA84, HLD24	Basal cell neoplasm, Bronchiectasis, Carcinoma, Diffuse interstitial pulmonary fibrosis, Gastroesophageal reflux disease, Honeycomb lung, Lung diseases, Pulmonary fibrosis, Hamman-rich syndrome
305	23266	ADGRL2	Adhesion G protein-coupled receptor L2	CIRL2, CL2, LEC1, LPHH1, LPHN2	Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Lupus erythematosus, Psoriasis, Ulcerative colitis
306	23284	ADGRL3	Adhesion G protein-coupled receptor L3	CIRL3, CL3, LEC3, LPHN3	Attention deficit hyperactivity disorder, Diabetes mellitus, Minimal brain dysfunction
307	23287	AGTPBP1	ATP/GTP binding carboxypeptidase 1	CCP1, CONDCA, NNA1	Cerebellar atrophy, Colorectal cancer, Developmental delay, Developmental regression, Dysphagia, High palate, Laryngomalacia, Motor delay, Neurodegenerative disorders with cerebellar atrophy, Nystagmus, Polyneuropathy, Pontoneocerebellar hypoplasia, Respiratory failure, Sleep apnea, Strabismus
308	23294	ANKS1A	Ankyrin repeat and sterile alpha motif domain containing 1A	ANKS1	Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Lupus erythematosus, Scleroderma
309	23305	ACSL6	Acyl-CoA synthetase long chain family member 6	ACS2, FACL6, LACS 6, LACS2, LACS5	Alzheimer disease, Leukemia, Myelodysplastic syndrome, Schizophrenia
310	2334	AFF2	ALF transcription elongation factor 2	FMR2, FMR2P, FRAXE, MRX2, OX19, XLID109	Autism, Camptodactyly of fingers, Congenital epicanthus, Dwarfism, Fragile x syndrome, Hand flapping, Macrocephaly, Mental retardation, Obsessive-compulsive disorder, Specific learning disorder, Stereotypy

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