GlyCosmos Portal

Displaying entries **76 - 100** of **320** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
100498555	LARGE xylosyl- and glucuronyltransferase 1	large1	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
496628	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
100379745	ALG14, UDP-N-acetylglucosaminyltransferase subunit	alg14	congenital myasthenic syndrome 15
549862	ALG13, UDP-N-acetylglucosaminyltransferase subunit-like	alg13l	developmental and epileptic encephalopathy 36
100145711	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
100145573	transmembrane and tetratricopeptide repeat containing 3	tmtc3	epilepsy lissencephaly 8
448549	regucalcin	rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
394883	glycogenin 1	gyg1	glycogen storage disease XV glycogen storage disease
594943	polypeptide N-acetylgalactosaminyltransferase 1	galnt1	heart valve disease
734090	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
100489739	heparan sulfate-glucosamine 3-sulfotransferase 6	hs3st6	hereditary angioedema
493398	exostosin like glycosyltransferase 3	extl3	hereditary multiple exostoses
100151709	exostosin glycosyltransferase 2	ext2	hereditary multiple exostoses
100145208	beta-1,4-N-acetyl-galactosaminyl transferase 1	b4galnt1	hereditary spastic paraplegia 26
100380028	phosphatidylinositol glycan anchor biosynthesis class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
100488466	polypeptide N-acetylgalactosaminyltransferase 3	galnt3	hyperphosphatemic familial tumoral calcinosis
548703	carbohydrate (chondroitin 4) sulfotransferase 12	chst12	hypertension
548887	UDP-glucose ceramide glucosyltransferase	ugcg	hypertension
550071	heparan sulfate 6-O-sulfotransferase 1	hs6st1	hypogonadotropic hypogonadism 15 with or without anosmia
548946	ALG10, alpha-1,2-glucosyltransferase	alg10	long QT syndrome 2 nonsyndromic deafness
496807	carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5	chst5	macular corneal dystrophy
100495636	carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6	chst6	macular corneal dystrophy
549139	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5	b4galt5	multiple sclerosis
548965	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 6	b4galt6	multiple sclerosis
100492673	carbohydrate (chondroitin 6) sulfotransferase 3	chst3	osteochondrodysplasia schizophrenia spondyloepiphyseal dysplasia with congenital joint dislocations

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