Genes | GeDiPNet - Gene Disease Pathway & Associations

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1061 to 1070 of 1170 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1061	91419	ATP23	ATP23 metallopeptidase and ATP synthase assembly factor homolog	KUB3, XRCC6BP1	Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Gout, Insomnia, Major depressive disorder, Sarcoidosis
1062	487	ATP2A1	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1	ATP2A, SERCA1	Asthma, Brody myopathy, Congestive heart failure, Heart failure, Hypogonadism, Obesity, Diabetes mellitus type 2
1063	488	ATP2A2	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	ATP2B, DAR, DD, RHABDO2, SERCA2	Acrokeratosis verruciformis, Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cardiomegaly, Obstructive pulmonary disease, Congestive heart failure, Crohn disease, Darier disease, Major depressive disorder, Experimental diabetes, Diabetes mellitus type 2, Diabetic cardiomyopathy View all (18 more)
1064	489	ATP2A3	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3	SERCA3	Atrial fibrillation, Experimental diabetes, Diabetes mellitus type 2, Oral cavity carcinoma
1065	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)
1066	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)
1067	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
1068	493	ATP2B4	ATPase plasma membrane Ca2+ transporting 4	ATP2B2, MXRA1, PMCA4, PMCA4b, PMCA4x	Obstructive sleep apnea syndrome, Ovarian cancer, Diabetes mellitus type 2
1069	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
1070	9914	ATP2C2	ATPase secretory pathway Ca2+ transporting 2	SPCA2	Attention deficit hyperactivity disorder, Obstructive pulmonary disease

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