GlyCosmos Portal

Displaying entries **326 - 350** of **1193** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
174262	Acetylcholine receptor subunit alpha-type acr-7	acr-7
181489	Disintegrin and metalloproteinase domain-containing protein adm-2	adm-2
181041	Disintegrin and metalloproteinase domain-containing protein 17 homolog	adm-4
181412	A disintegrin and metalloproteinase with thrombospondin motifs adt-1;Peptidase M12B domain-containing protein	adt-1
181022	A disintegrin and metalloproteinase with thrombospondin motifs adt-2;Peptidase M12B domain-containing protein	adt-2
188491	G-protein coupled receptor aex-2	aex-2
173358	Endoprotease aex-5	aex-5
174123	Cell fusion protein aff-1	aff-1
3565243	Agrin	agr-1
176788	Fructose-bisphosphate aldolase 1	aldo-1	autoimmune disease of the nervous system borna disease hepatocellular carcinoma hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
175827	Fructose-bisphosphate aldolase 2	aldo-2	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
172855	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	algn-10	long QT syndrome 2 nonsyndromic deafness
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	congenital disorder of glycosylation Ip
179185	Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase	algn-12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
179890	UDP-N-acetylglucosamine transferase subunit ALG13	algn-13	developmental and epileptic encephalopathy 36
187398	UDP-N-acetylglucosamine transferase subunit ALG14	algn-14	congenital myasthenic syndrome 15
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
175065	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	algn-3	congenital disorder of glycosylation Id congenital disorder of glycosylation
178822	Dolichyl-phosphate beta-glucosyltransferase;dolichyl-phosphate beta-glucosyltransferase	algn-5	congenital disorder of glycosylation type I polycystic kidney disease
182392	putative dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
190436	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	algn-7	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
174542	Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
180749	Alpha-mannosidase	aman-1

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