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

1831 to 1840 of 12229 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1831	1261	CNGA3	Cyclic nucleotide gated channel subunit alpha 3	ACHM2, CCNC1, CCNCa, CCNCalpha, CNCG3, CNG3	Achromatopsia, Color blindness, Cone dystrophy, Cone monochromatism, Cone-rod dystrophy, Disorder of eye, Dyschromatopsia, Exotropia, Hemeralopia, Hyperopia, Macular degeneration, Nyctalopia, Nystagmus, Pendular nystagmus, Retinal dystrophy, Rod-cone dystrophy View all (1 more)
1832	126129	CPT1C	Carnitine palmitoyltransferase 1C	CATL1, CPT I-C, CPT1-B, CPT1P, CPTI-B, CPTIC, SPG73	Autoimmune diseases, Distal lower limb amyotrophy, Hypothyroidism, Melanoma, Nervous system diseases, Spastic paraplegia
1833	126133	ALDH16A1	Aldehyde dehydrogenase 16 family member A1	-	Gout, Hyperuricemia
1834	126205	NLRP8	NLR family pyrin domain containing 8	CLR19.2, NALP8, NOD16, PAN4	Breast cancer, Colorectal cancer
1835	126208	ZNF787	Zinc finger protein 787	TIP20	Leukemia
1836	126248	WDR88	WD repeat domain 88	PQWD	Breast cancer
1837	126306	JSRP1	Junctional sarcoplasmic reticulum protein 1	JP-45, JP45	Sclerocystic ovaries, Polycystic ovary syndrome
1838	126326	GIPC3	GIPC PDZ domain containing family member 3	C19orf64, DFNB15, DFNB72, DFNB95	Deafness, Hearing loss, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Sensorineural hearing loss
1839	126328	NDUFA11	NADH:ubiquinone oxidoreductase subunit A11	B14.7, CI-B14.7, MC1DN14	Brain atrophy, Cerebral atrophy, Developmental delay, Diabetes mellitus, Epileptic encephalopathy, Hearing loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated complex i deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy View all (5 more)
1840	126393	HSPB6	Heat shock protein family B (small) member 6	HEL55, Hsp20, PPP1R91	Heart diseases

«««...182 183184185 186...»»»