Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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"

1031 to 1040 of 1338 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1031	79603	CERS4	Ceramide synthase 4	LASS4, Trh1	Kidney disease, Kidney failure
1032	79682	CENPU	Centromere protein U	CENP50, CENPU50, KLIP1, MLF1IP, PBIP1	Kawasaki disease, Liver carcinoma, Lupus erythematosus
1033	797	CALCB	Calcitonin related polypeptide beta	CALC2, CGRP-II, CGRP2	Breast cancer, Diverticular diseases, Diverticulitis
1034	79709	COLGALT1	Collagen beta(1-O)galactosyltransferase 1	BSVD3, ColGalT 1, GLT25D1	Cerebral atrophy, Developmental delay, Leukoencephalopathy, Narcolepsy, Spastic quadriplegia
1035	79780	CCDC82	Coiled-coil domain containing 82	HSPC048	Parkinson disease
1036	79789	CLMN	Calmin	-	Alzheimer disease
1037	79800	CARF	Calcium responsive transcription factor	ALS2CR8, NYD-SP24	Bipolar disorder, Coronary artery disease, Mental depression, Migraine, Schizophrenia
1038	79823	CAMKMT	Calmodulin-lysine N-methyltransferase	C2orf34, CLNMT, CaM KMT, Cam, KMT	2p21 microdeletion syndrome, 2p21 microdeletion syndrome without cystinuria, Bipolar disorder, Cystinuria, Development disorder, Developmental delay, Developmental dyspraxia, Frontal bossing, Hypoglycemia, Hypogonadism, Hypotonia-cystinuria syndrome, Learning disorders, Luft disease, Megaconial myopathies, Mental retardation View all (4 more)
1039	79827	CLMP	CXADR like cell adhesion molecule	ACAM, ASAM, CSBM, CSBS	Congenital malrotation of intestine, Congenital shortened small intestine, Dwarfism, Hypotrichosis, Impaired cognition, Intestinal pseudoobstruction, Lipoatrophy, Lipodystrophy, Paralytic ileus, Visceral myopathy
1040	79839	CCDC102B	Coiled-coil domain containing 102B	ACY1L, AN, C18orf14, HsT1731	Bipolar disorder, Schizoaffective disorder, Schizophrenia, Stroke

«««...102 103104105 106...»»»