GlyCosmos Portal

Displaying entries **51 - 75** of **320** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
496641	beta-1,3-N-acetylgalactosaminyltransferase 2	b3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
496754	monoacylglycerol O-acyltransferase 2, gene 1	mogat2
496807	carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5	chst5	macular corneal dystrophy
496815	mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase	mgat1
496877	glycogenin 2	gyg2
496884	dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
496940	heparan sulfate-glucosamine 3-sulfotransferase 1	hs3st1
496948	ALG6, alpha-1,3-glucosyltransferase	alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
548388	ALG8, alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
548391	fucosyltransferase 9 (alpha (1,3) fucosyltransferase)	fut9	candidiasis
548703	carbohydrate (chondroitin 4) sulfotransferase 12	chst12	hypertension
548704	protein phosphatase 1 regulatory subunit 3B	ppp1r3b	alcohol use disorder
548849	Beta-1,3-galactosyltransferase 6	b3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
548874	ALG12, alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
548887	UDP-glucose ceramide glucosyltransferase	ugcg	hypertension
548938	ADP-ribosylserine hydrolase	adprs	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
548940	mannose-P-dolichol utilization defect 1	mpdu1	congenital disorder of glycosylation If
548946	ALG10, alpha-1,2-glucosyltransferase	alg10	long QT syndrome 2 nonsyndromic deafness
548965	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 6	b4galt6	multiple sclerosis
549139	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5	b4galt5	multiple sclerosis
549340	glycosyltransferase 8 domain containing 1	glt8d1
549416	alpha-1,4-N-acetylglucosaminyltransferase	a4gnt	pancreatic cancer
549418	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 2	b4galt1.2	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
549437	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 3	abo.3	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome

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