Genes | GeDiPNet - Gene Disease Pathway & Associations

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2651 to 2660 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2651	81570	CLPB	ClpB family mitochondrial disaggregase	ANKCLB, ANKCLP, HSP78, MEGCANN, MGCA7, MGCA7A, SCN9, SKD3	3-methylglutaconic aciduria, Severe congenital neutropenia, Leigh syndrome, Microcytic anemia, Neutropenia, Obesity, Scoliosis, Congenital neutropenia
2652	8192	CLPP	Caseinolytic mitochondrial matrix peptidase proteolytic subunit	DFNB81, PRLTS3	Alzheimer disease, Gonadal dysgenesis, Peripheral arterial disease, Perrault syndrome, Xq27.3 q28 duplication syndrome
2653	1208	CLPS	Colipase	-	Diabetes mellitus type 2
2654	1209	CLPTM1	CLPTM1 regulator of GABA type A receptor forward trafficking	-	Alzheimer disease, Iga nephropathy, Metabolic syndrome, Pancreatic neoplasms, Diabetes mellitus type 2
2655	81037	CLPTM1L	CLPTM1 like	CRR9	Basal cell carcinoma, Benign prostatic hyperplasia, Non-small-cell lung carcinoma, Cervical cancer, Cervical intraepithelial neoplasia, Lymphocytic leukemia, Colorectal cancer, Melanoma, Head and neck cancer, Keratinocyte carcinoma, Lung cancer, Lung neoplasms, Mouth neoplasms, Nasopharyngeal neoplasms, Non-melanoma skin carcinoma View all (15 more)
2656	10845	CLPX	Caseinolytic mitochondrial matrix peptidase chaperone subunit X	EPP2	Alzheimer disease, Dementia, Erythropoietic protoporphyria
2657	7401	CLRN1	Clarin 1	RP61, USH3, USH3A	Branchiootorenal syndrome, Hearing impairment, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome
2658	645104	CLRN2	Clarin 2	DFNB117	Isolated sensorineural deafness, Deafness, Hearing loss, Nonsyndromic hearing loss
2659	119467	CLRN3	Clarin 3	TMEM12, USH3AL1	Parkinson disease
2660	22883	CLSTN1	Calsyntenin 1	ALC-ALPHA, CDHR12, CST-1, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2	Alzheimer disease, Asthma

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