Genes | GeDiPNet - Gene Disease Pathway & Associations

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11591 to 11600 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11591	6337	SCNN1A	Sodium channel epithelial 1 subunit alpha	BESC2, ENaCa, ENaCalpha, LIDLS3, PHA1B1, SCNEA, SCNN1	Ankylosing spondylitis, Autism, Autoinflammatory syndrome, Bronchiectasis, Brugada syndrome, Crohn disease, Cystic fibrosis, Hypertension, Inflammatory bowel disease, Liddle syndrome, Lung disease, Obesity, Polycystic ovary syndrome, Preeclampsia, Biliary cholangitis View all (4 more)
11592	6338	SCNN1B	Sodium channel epithelial 1 subunit beta	BESC1, ENaCb, ENaCbeta, LIDLS1, PHA1B2, SCNEB, beta-ENaC, beta-NaCH	Autism, Bronchiectasis, Cystic fibrosis, Diabetic ketoacidosis, Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young, Hypertension, Liddle syndrome, Lung disease, Nephrolithiasis, Pseudohypoparathyroidism, Schizophrenia, Diabetes mellitus type 1
11593	6340	SCNN1G	Sodium channel epithelial 1 subunit gamma	BESC3, ENaCg, ENaCgamma, LDLS2, PHA1, PHA1B3, SCNEG	Autism, Bronchiectasis, Cystic fibrosis, Focal segmental glomerulosclerosis, Hypertension, Hypotension, Liddle syndrome, Pseudohypoparathyroidism
11594	6341	SCO1	Synthesis of cytochrome C oxidase 1	MC4DN4, SCOD1	Brain disease, Cytochrome c oxidase deficiency, Heart disease, Leigh syndrome, Liver disease, Liver failure, Mitochondrial complex deficiency, Mitochondrial disease
11595	9997	SCO2	Synthesis of cytochrome C oxidase 2	CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase	Charcot-marie-tooth disease, Brain disease, Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cardiomyopathy, Dilated cardiomyopathy, Cytochrome c oxidase deficiency, Hypertrophic cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial dna depletion syndrome, Mitochondrial encephalomyopathy, Myopia, Retinitis pigmentosa
11596	60592	SCOC	Short coiled-coil protein	HRIHFB2072, SCOCO, UNC-69	Astrocytoma, Central nervous system cancer, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Colorectal cancer
11597	6342	SCP2	Sterol carrier protein 2	NLTP, NSL-TP, SCOX, SCP-2, SCP-CHI, SCP-X, SCPX	Sterol carrier protein 2 deficiency, Dystonia, Leukodystrophy, Polyneuropathy, Hearing loss
11598	59342	SCPEP1	Serine carboxypeptidase 1	HSCP1, RISC	Colorectal cancer, Glaucoma
11599	23513	SCRIB	Scribble planar cell polarity protein	CRIB1, SCRB1, SCRIB1, Vartul, oSCRIB	Autism, Gout, Neural tube defect
11600	9805	SCRN1	Secernin 1	SES1	Obesity, Osteoarthritis, Psoriasis, Stomach neoplasms

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