Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "C"

1791 to 1800 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1791	51571	CYRIB	CYFIP related Rac1 interactor B	BM-009, CYRI, CYRI-B, FAM49B, L1	Alzheimer disease, Androgenetic alopecia, Colorectal cancer, Heart failure, Liver cirrhosis, Migraine, Parkinson disease, Post-traumatic stress disorder, Rheumatoid arthritis, Schizophrenia
1792	192668	CYS1	Cystin 1	-	Atrial fibrillation, Polycystic kidney disease, Bronchitis, Obstructive pulmonary disease, Gout
1793	10800	CYSLTR1	Cysteinyl leukotriene receptor 1	CYSLT1, CYSLT1R, CYSLTR, HMTMF81	Asthma, Coronary artery disease, Rhinitis
1794	57105	CYSLTR2	Cysteinyl leukotriene receptor 2	CYSLT2, CYSLT2R, GPCR21, HG57, HPN321, KPG_011, PSEC0146, hGPCR21	Asthma, Atrial fibrillation, Ovarian epithelial cancer, Ovarian cancer, Pulmonary fibrosis, Juvenile idiopathic arthritis, Uveal melanoma
1795	84418	CYSTM1	Cysteine rich transmembrane module containing 1	C5orf32, ORF1-FL49	Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Hypertension, Liver cirrhosis, Major depressive disorder, Post-traumatic stress disorder, Schizophrenia
1796	4519	CYTB	Mitochondrially encoded cytochrome b	MTCYB	Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, S, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss
1797	6775065	CYTB	-	-	Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, S, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss
1798	8923205	CYTB	-	-	Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, S, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss
1799	9267	CYTH1	Cytohesin 1	B2-1, CYTOHESIN-1, D17S811E, PSCD1, SEC7	Atrial fibrillation, Coronary artery disease, Heart failure, Major depressive disorder, Diabetes mellitus, type 2, Ulcerative colitis
1800	9266	CYTH2	Cytohesin 2	ARNO, CTS18, CTS18.1, PSCD2, PSCD2L, SEC7L, Sec7p-L, Sec7p-like, cytohesin-2	Iga nephropathy

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