Genes | GeDiPNet - Gene Disease Pathway & Associations

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691 to 700 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
691	10241	CALCOCO2	Calcium binding and coiled-coil domain 2	NDP52	Colorectal cancer, Colorectal neoplasms, Diabetes mellitus
692	10242	KCNMB2	Potassium calcium-activated channel subfamily M regulatory beta subunit 2	-	Amyotrophic lateral sclerosis, Bipolar disorder, Lateral sclerosis, Mental disorders, Mental depression, Psychosis, Schizophrenia
693	10243	GPHN	Gephyrin	GEPH, GPH, GPHRYN, HKPX1, MOCODC	Cerebellar hypoplasia, Cerebral atrophy, Combined molybdoflavoprotein enzyme deficiency, Congenital exomphalos, Developmental delay, Dyssomnia, Epileptic encephalopathy, Eosinophilia, Gastroesophageal reflux disease, Hereditary hyperekplexia, Hiatal hernia, Hyperekplexia, Mental depression, Mental retardation, Molybdenum cofactor deficiency View all (5 more)
694	10246	SLC17A2	Solute carrier family 17 member 2	NPT3	Ankylosing spondylitis, Gout, Gouty arthritis, Liver cirrhosis, Liver fibrosis
695	102465534	MIR6886	MicroRNA 6886	hsa-mir-6886	Hypercholesterolemia, Hyperlipoproteinemia
696	102465802	MIR7704	MicroRNA 7704	hsa-mir-7704	Diabetes mellitus
697	102466251	MIR8061	MicroRNA 8061	hsa-mir-8061	Diabetes mellitus
698	102466270	MIR6741	MicroRNA 6741	hsa-mir-6741	Diabetes mellitus
699	102466656	MIR6500	MicroRNA 6500	hsa-mir-6500	Atrial fibrillation, Paroxysmal atrial fibrillation
700	102466739	MIR6803	MicroRNA 6803	hsa-mir-6803	Diabetes mellitus

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