Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1471 to 1480 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1471	57482	CRACD	Capping protein inhibiting regulator of actin dynamics	CRAD, KIAA1211	Coronary artery disease, Lung cancer, Obesity, Scoliosis, Squamous cell carcinoma
1472	343990	CRACDL	CRACD like	C2orf55, KIAA1211L	Bipolar disorder
1473	84766	CRACR2A	Calcium release activated channel regulator 2A	EFCAB4B, RAB46	Liver cirrhosis, Combined immunodeficiency disease, Male infertility, Nonalcoholic fatty liver disease, Periodontitis, Sialolithiasis
1474	283229	CRACR2B	Calcium release activated channel regulator 2B	EFCAB4A	Bronchitis, Obstructive pulmonary disease, Obesity
1475	8738	CRADD	CARD and death domain containing adaptor protein	MRT34, RAIDD	Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Nonsyndromic intellectual disability, Bone fracture, Renal cell carcinoma, Dementia, Arrhythmogenic right ventricular dysplasia, Global developmental delay, Hypertension, Intellectual developmental disorder, Osteoarthritis, Scoliosis, Diabetes mellitus, type 2
1476	57585	CRAMP1	Cramped chromatin regulator 1	CRAMP1L, HN1L, TCE4	Atrial fibrillation, Epilepsy, Prostate cancer
1477	1384	CRAT	Carnitine O-acetyltransferase	CAT, CAT1, NBIA8	Eczema, Carnitine acetyltransferase deficiency, Neurodegeneration with brain iron accumulation, Pelvic organ prolapse
1478	23418	CRB1	Crumbs cell polarity complex component 1	CRB1-A, CRB1-B, CRB1-C, LCA8, RP12	Leber congenital amaurosis, Ankylosing spondylitis, Anorexia nervosa, Asthma, Autoimmune disease, Autoimmune thyroid disease, Retinitis pigmentosa, Bestrophinopathy, Celiac disease, Color vision deficiency, Common variable immunodeficiency, Cone dystrophy, Cone-rod dystrophy, Crohn disease, Eating disorder View all (19 more)
1479	286204	CRB2	Crumbs cell polarity complex component 2	FSGS9, VMCKD	Astrocytoma, Central nervous system cancer, Cystic kidney disease with ventriculomegaly, Dementia, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glioblastoma, Glioma, Hereditary steroid-resistant nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, focal segmental type, Oligodendroglioma, Retinitis pigmentosa View all (4 more)
1480	51185	CRBN	Cereblon	MRT2, MRT2A	Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Bipolar disorder, Cholecystitis, Cholecystolithiasis, Congenital neurologic anomalies, Eating disorder, Intellectual developmental disorder, Multiple myeloma, Osteoarthritis, Pancreatic cancer, Willis-ekbom disease, Scoliosis View all (4 more)

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