Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1141 to 1150 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1141	84342	COG8	Component of oligomeric golgi complex 8	CDG2H, DOR1	Alternating esotropia, Brainstem atrophy, Cerebellar atrophy, Clinodactyly, Congenital clubfoot, Congenital disorder of glycosylation, Congenital epicanthus, Developmental delay, Developmental regression, Encephalopathy, Epileptic encephalopathy, Food intolerance, Hematomas, Hypoglycemia, Mental retardation View all (6 more)
1142	8436	CAVIN2	Caveolae associated protein 2	PS-p68, SDPR, SDR, cavin-2	Colonic aganglionosis, Congenital intestinal aganglionosis, Hirschsprung disease
1143	844	CASQ1	Calsequestrin 1	CASQ, CSQ1, PDIB1, VMCQA	Myopathy, Tubular aggregate myopathy, Vacuolar myopathy with casq1 aggregates
1144	84433	CARD11	Caspase recruitment domain family member 11	BENTA, BIMP3, CARMA1, IMD11, IMD11A, PPBL	Asthma, B-cell expansion with nfkb and t-cell anergy, Chromophobe carcinoma, Dermatitis, Immunodeficiency 11b with atopic dermatitis, Diffuse lymphoma, Eczema, Eosinophilia, Granulomatous slack skin, Immunodeficiency, Immunologic deficiency syndromes, Intracranial aneurysm, Lymphocytosis, Lymphoma, Papillary renal carcinoma View all (6 more)
1145	845	CASQ2	Calsequestrin 2	PDIB2	Atrial fibrillation, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Hypertrophic cardiomyopathy, Paroxysmal atrial fibrillation, Stress-induced polymorphic ventricular tachycardia, Ventricular tachycardia
1146	8450	CUL4B	Cullin 4B	CUL-4B, MRXHF2, MRXS15, MRXSC, SFM2	Acanthosis nigricans, Cubitus valgus, Atrophy, Blepharophimosis, Camptodactyly of fingers, Congenital epicanthus, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Distal lower limb amyotrophy, Dwarfism, Dysmorphic features, Gynecomastia, High palate, Hypogonadism View all (18 more)
1147	8451	CUL4A	Cullin 4A	-	Atrial fibrillation, Bipolar disorder, Paroxysmal atrial fibrillation, Stevens-johnson syndrome
1148	8452	CUL3	Cullin 3	CUL-3, NEDAUS, PHA2E	Dysmorphic features, Hyperchloremia, Hypertension, Melanoma, Multiple congenital anomalies, Neurodevelopmental disorders, Prostatic neoplasms, Prostate cancer, Pseudohypoaldosteronism, Schizophrenia
1149	84529	CDIN1	CDAN1 interacting nuclease 1	C15orf41, HH114	Anemia, Congenital dyserythropoietic anemia, Erythroid hyperplasia
1150	8453	CUL2	Cullin 2	-	Inflammatory bowel disease

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