Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

71 to 80 of 912 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
71	10555	AGPAT2	1-acylglycerol-3-phosphate O-acyltransferase 2	1-AGPAT2, BSCL, BSCL1, LPAAB, LPAAT-beta, LPLAT2	Generalized lipodystrophy, Lipodystrophy, Neonatal diabetes mellitus
72	10564	ARFGEF2	ARF guanine nucleotide exchange factor 2	BIG2, PVNH2, dJ1164I10.1	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Coronary artery disease, Dyslexia, Global developmental delay, Hepatitis b, Periventricular nodular heterotopia, Hydrocephalus, Intellectual developmental disorder, Major depressive disorder, Myocardial infarction, Periventricular heterotopia with microcephaly, autosomal recessive, Periventricular heterotopia, x-linked, Periventricular laminar heterotopia View all (3 more)
73	10565	ARFGEF1	ARF guanine nucleotide exchange factor 1	ARFGEP1, BIG1, DEDISB, P200	Chronic central serous retinopathy, Developmental delay with impaired growth and dysmorphic facies, Developmental disability, Global developmental delay, Intellectual developmental disorder, Joubert syndrome, Neurodevelopmental disorders, Schizophrenia, Seizures
74	10566	AKAP3	A-kinase anchoring protein 3	AKAP 110, AKAP110, CT82, FSP95, HEL159, PRKA3, SOB1, SPGF82	Color vision deficiency, Male infertility large polyploid spermatozoa, Spermatogenic failure
75	10620	ARID3B	AT-rich interaction domain 3B	BDP, DRIL2	Central nervous system cancer, Craniofacial microsomia, Endometriosis, Glioblastoma, Glioma, Iga nephropathy, Nephrotic syndrome, Squamous cell carcinoma, Diabetes mellitus, type 2
76	10632	ATP5MG	ATP synthase membrane subunit g	ATP5JG, ATP5L	Major depressive disorder
77	107	ADCY1	Adenylate cyclase 1	AC1, DFNB44	Isolated sensorineural deafness, Nonsyndromic hearing loss, Bipolar disorder, Color vision deficiency, Deafness, Duchenne muscular dystrophy, Hearing loss, Hyperkinesia, Polycystic ovary syndrome, Schizophrenia, Small cell lung carcinoma, Substance abuse, Diabetes mellitus, type 2
78	10717	AP4B1	Adaptor related protein complex 4 subunit beta 1	BETA-4, CPSQ5, SPG47	Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Basal cell carcinoma, Breast cancer, Congenital neurologic anomalies�, Intellectual developmental disorder, Obesity, Intellectual disability, Skin neoplasm, Spastic paraplegia, Hereditary spastic paraplegia
79	10768	AHCYL1	Adenosylhomocysteinase like 1	DCAL, IRBIT, PPP1R78, PRO0233, XPVKONA	Alzheimer disease, Attention deficit hyperactivity disorder, Metabolic syndrome, Ocular hypotension, Substance abuse, Diabetes mellitus, type 2
80	10777	ARPP21	CAMP regulated phosphoprotein 21	ARPP-21, R3HDM3, RCS, TARPP	Amyotrophic lateral sclerosis, Monomelic amyotrophy, Asthma, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Obstructive pulmonary disease, Gastroesophageal reflux disease, Heart failure, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Osteoarthritis View all (2 more)

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