GlyCosmos Portal

Displaying entries **1 - 25** of **320** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
448400	xylosyltransferase II	xylt2	polycystic kidney disease pseudoxanthoma elasticum
100145490	xylosyltransferase I	xylt1	Desbuquois dysplasia kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
100144979	xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7	b4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
100495920	xyloside xylosyltransferase 1	xxylt1
100496425	uronyl-2-sulfotransferase	ust
116407726	uncharacterized LOC116407726	LOC116407726
100493718	uncharacterized LOC100493718	LOC100493718
100038162	triosephosphate isomerase 1	tpi1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
100158586	transmembrane and tetratricopeptide repeat containing 4	tmtc4	autosomal recessive nonsyndromic deafness
100145573	transmembrane and tetratricopeptide repeat containing 3	tmtc3	epilepsy lissencephaly 8
100124656	transmembrane and tetratricopeptide repeat containing 2	tmtc2
100498549	transmembrane and tetratricopeptide repeat containing 1	tmtc1
448579	trans-1,2-dihydrobenzene-1,2-diol dehydrogenase like	dhdhl
100145200	solute carrier family 23 (ascorbic acid transporter), member 2	slc23a2
100145540	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
448549	regucalcin	rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
549645	queuine tRNA-ribosyltransferase accessory subunit 2	qtrt2
394694	queuine tRNA-ribosyltransferase 1	qtrt1
100125092	provisional ortholog of heparan sulfate-glucosamine 3-sulfotransferase 1	XB5817455
100486342	provisional ortholog of glucosaminyl (N-acetyl) transferase 3, mucin type	XB990816
100496837	provisional ortholog of core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	XB5871033	autoimmune disease of blood
100489267	provisional ortholog of UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	XB5969542
100490100	protein-O-mannosyltransferase 2	pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
448433	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
407879	protein phosphatase 1, catalytic subunit, gamma isozyme	ppp1cc	cancer congestive heart failure type 2 diabetes mellitus

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