Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

1061 to 1070 of 1165 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1061	490	ATP2B1	ATPase plasma membrane Ca2+ transporting 1	MRD66, PMCA1, PMCA1kb	Atrial fibrillation, Autism, Brain aneurysm, Cancer, Cardiovascular disease, Cataract, Ischemic heart disease, Congenital clubfoot, Coronary artery disease, Diabetes mellitus, Hypertension, Heart disease, Heart failure, Hypocalcemia, Intellectual developmental disorder View all (8 more)
1062	491	ATP2B2	ATPase plasma membrane Ca2+ transporting 2	DFNA82, PMCA2, PMCA2a, PMCA2i	Asthma, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Bipolar disorder, Color vision deficiency, Deafness, Developmental and epileptic encephalopathy, Hearing impairment, Hearing loss, Insomnia, Neurodevelopmental disorder, Progressive supranuclear palsy, Prostate cancer, Schizophrenia View all (2 more)
1063	492	ATP2B3	ATPase plasma membrane Ca2+ transporting 3	CFAP39, CLA2, OPCA, PMCA3, PMCA3a, SCAX1	Arthrogryposis multiplex congenita, Cushing syndrome, Dental caries, Global developmental delay, Hyperaldosteronism, Hypertension, Intellectual developmental disorder, Neurodevelopmental disorder, Oropharyngeal dysphagia, Pena-shokeir syndrome , Spastic ataxia, Spinocerebellar ataxia, x-linked, Diabetes mellitus type 2, X-linked non progressive cerebellar ataxia, X-linked progressive cerebellar ataxia
1064	493	ATP2B4	ATPase plasma membrane Ca2+ transporting 4	ATP2B2, MXRA1, PMCA4, PMCA4b, PMCA4x	Obstructive sleep apnea syndrome, Ovarian cancer, Diabetes mellitus type 2
1065	27032	ATP2C1	ATPase secretory pathway Ca2+ transporting 1	ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1	Alzheimer disease, Autoimmune musculoskeletal system disorder, Benign pemphigus, Insomnia, Benign familial pemphigus, Willis-ekbom disease, Systemic lupus erythematosus
1066	9914	ATP2C2	ATPase secretory pathway Ca2+ transporting 2	SPCA2	Attention deficit hyperactivity disorder, Obstructive pulmonary disease
1067	495	ATP4A	ATPase H+/K+ transporting subunit alpha	ATP6A	Intrahepatic cholestasis of pregnancy
1068	496	ATP4B	ATPase H+/K+ transporting subunit beta	ATP6B	Autoimmune gastritis, Gastritis
1069	498	ATP5F1A	ATP synthase F1 subunit alpha	ATP5A, ATP5A1, ATP5AL2, ATPM, COXPD22, HEL-S-123m, MC5DN4, MC5DN4A, MC5DN4B, MOM2, OMR, ORM, hATP1	Alzheimer disease, Combined oxidative phosphorylation deficiency, Mitochondrial complex deficiency, Mitochondrial disease
1070	506	ATP5F1B	ATP synthase F1 subunit beta	ATP5B, ATPMB, ATPSB, HEL-S-271, HUMOP2	Alzheimer disease, Hypoxia, Kidney failure, Nonalcoholic fatty liver disease, Spinocerebellar ataxia

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