Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1161 to 1170 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1161	1198	CLK3	CDC like kinase 3	PHCLK3, PHCLK3/152	Urinary bladder cancer
1162	79789	CLMN	Calmin	-	Alzheimer disease, Venous thromboembolism
1163	79827	CLMP	CXADR like cell adhesion molecule	ACAM, ASAM, CSBM, CSBS	Breast cancer, Central nervous system cancer, Colorectal cancer, Congenital short bowel syndrome, Glaucoma, Glioblastoma, Glioma, Hemorrhoid, Intestinal obstruction, Oligodendroglioma, Partial epilepsy, Post-operative acute kidney injury
1164	1201	CLN3	CLN3 lysosomal/endosomal transmembrane protein, battenin	BTN1, BTS, JNCL, SLC29B1	Asthma, Bipolar disorder, Bullous pemphigoid, Neuronal ceroid lipofuscinosis, Cone-rod dystrophy, Crohn disease, Progressive myoclonic epilepsy, Hypothyroidism, Inflammatory bowel disease, Intellectual developmental disorder, Retinitis pigmentosa, Stomach neoplasms, Diabetes mellitus type 1, Diabetes mellitus type 2, Visual disorder
1165	1203	CLN5	CLN5 lysosomal BMP synthase	-	Neuronal ceroid lipofuscinosis, Neurodevelopmental disorder, Pontocerebellar hypoplasia, Visual disorder
1166	54982	CLN6	CLN6 transmembrane ER protein	CLN4A, CLN6A, HsT18960, nclf	Atrophy, Neuronal ceroid lipofuscinosis, Congenital neurologic anomalies, Cystic fibrosis, Motor skills disorder, Neurodevelopmental disorder, Spastic ataxia, Visual disorder
1167	2055	CLN8	CLN8 transmembrane ER and ERGIC protein	C8orf61, EPMR, TLCD6	Autism, Neuronal ceroid lipofuscinosis, Gaucher disease, Intellectual developmental disorder, Major depressive disorder
1168	116449	CLNK	Cytokine dependent hematopoietic cell linker	MIST	Autoimmune thyroid disease, Esophageal disease, Esophageal ulcer, Gout, Hyperuricemia, Hypothyroidism, Osteonecrosis of the femoral head, Psychiatric disorders, Rheumatoid arthritis, Sclerosing cholangitis, Systemic lupus erythematosus, Thyroid disease, Hypertension, Vitiligo
1169	1207	CLNS1A	Chloride nucleotide-sensitive channel 1A	CLCI, CLNS1B, ICln	Alzheimer disease, Melanoma
1170	9575	CLOCK	Clock circadian regulator	KAT13D, bHLHe8	Alzheimer disease, Androgenetic alopecia, Bipolar disorder, Coronary artery disease, Major depressive disorder, Mood disorder, Schizophrenia, Seasonal affective disorder, Depression

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