GlyCosmos Portal

Displaying entries **126 - 150** of **358** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
767756	UDP glucuronosyltransferase 5 family, polypeptide A2	ugt5a2
767705	UDP glucuronosyltransferase 2 family, polypeptide A5	ugt2a5
751669	UDP glucuronosyltransferase 5 family, polypeptide C2	ugt5c2
751653	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4	st6galnac4
751635	ALG5 dolichyl-phosphate beta-glucosyltransferase	alg5	polycystic kidney disease
724080	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5	b4galt5	multiple sclerosis
724006	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
678597	UDP glucuronosyltransferase 5 family, polypeptide B6	ugt5b6
652952	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2	ogt.2	aortic valve stenosis non-syndromic X-linked intellectual disability 106
641495	protein O-glucosyltransferase 1	poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
641488	UDP glucuronosyltransferase 1 family, polypeptide A1	ugt1a1
641479	UDP glucuronosyltransferase 5 family, polypeptide A1	ugt5a1
619261	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1	b3gntl1
572324	UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6	b3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
571876	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
571426	fukutin related protein	fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
571246	heparan sulfate (glucosamine) 3-O-sulfotransferase 2	hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
571003	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1b	b3galt1b
570913	UDP glucuronosyltransferase 5 family, polypeptide G1	ugt5g1
570828	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase b	mgat3b
570459	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b	ndst1b	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
570248	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2	galnt2	congenital disorder of glycosylation type II
569769	protein-O-mannosyltransferase 1	pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
569494	ALG12 alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
569353	heparan sulfate 6-O-sulfotransferase 3b	hs6st3b

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