GlyCosmos Portal

Displaying entries **76 - 100** of **478** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
101027298	polypeptide N-acetylgalactosaminyltransferase 2 S homeolog	galnt2.S	congenital disorder of glycosylation type II
108716128	polypeptide N-acetylgalactosaminyltransferase 2 L homeolog	galnt2.L	congenital disorder of glycosylation type II
444674	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase S homeolog	mgat2.S	congenital disorder of glycosylation type IIa
414590	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase L homeolog	mgat2.L	congenital disorder of glycosylation type IIa
108706813	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 2 S homeolog	b4galt1.2.S	congenital disorder of glycosylation type IId congenital disorder of glycosylation
108712216	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 2 L homeolog	b4galt1.2.L	congenital disorder of glycosylation type IId congenital disorder of glycosylation
108706812	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 1 S homeolog	b4galt1.1.S	congenital disorder of glycosylation type IId congenital disorder of glycosylation
108712215	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 1 L homeolog	b4galt1.1.L	congenital disorder of glycosylation type IId congenital disorder of glycosylation
446820	ribitol xylosyltransferase 1 S homeolog	rxylt1.S	congenital muscular dystrophy-dystroglycanopathy type A10
431874	beta-1,3-N-acetylgalactosaminyltransferase 2 L homeolog	b3galnt2.L	congenital muscular dystrophy-dystroglycanopathy type A11
496338	protein-O-mannose kinase L homeolog	pomk.L	congenital muscular dystrophy-dystroglycanopathy type A12 muscular dystrophy-dystroglycanopathy type C12
108713949	beta-1,4-glucuronyltransferase 1 L homeolog	b4gat1.L	congenital muscular dystrophy-dystroglycanopathy type A13
108712551	LARGE xylosyl- and glucuronyltransferase 1 S homeolog	large1.S	congenital muscular dystrophy-dystroglycanopathy type A6 muscular dystrophy-dystroglycanopathy type B6
108704366	LARGE xylosyl- and glucuronyltransferase 1 L homeolog	large1.L	congenital muscular dystrophy-dystroglycanopathy type A6 muscular dystrophy-dystroglycanopathy type B6
444520	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) L homeolog	pomgnt2.L	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
108714370	ALG14, UDP-N-acetylglucosaminyltransferase subunit L homeolog	alg14.L	congenital myasthenic syndrome 15
108715652	ALG14, UDP-N-acetylglucosaminyltransferase subunit S homeolog	alg14.S	congenital myasthenic syndrome 15
108698403	ALG13 UDP-N-acetylglucosaminyltransferase subunit L homeolog	alg13.L	developmental and epileptic encephalopathy 36
108711378	phosphatidylinositol glycan anchor biosynthesis class B L homeolog	pigb.L	developmental and epileptic encephalopathy 80
734564	phosphatidylinositol glycan anchor biosynthesis class B S homeolog	pigb.S	developmental and epileptic encephalopathy 80
379886	citrate synthase L homeolog	cs.L	dilated cardiomyopathy hypertrophic cardiomyopathy
779133	glycogenin 1 L homeolog	gyg1.L	glycogen storage disease XV glycogen storage disease
446485	glycogenin 1 S homeolog	gyg1.S	glycogen storage disease XV glycogen storage disease
100037183	UDP glucuronosyltransferase 1 family, polypeptide A6 S homeolog	ugt1a6.S	hepatitis B
495489	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 S homeolog	plod3.S	hepatocellular carcinoma

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