GlyCosmos Portal

Displaying entries **26 - 50** of **320** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
548946	ALG10, alpha-1,2-glucosyltransferase	alg10	long QT syndrome 2 nonsyndromic deafness
550071	heparan sulfate 6-O-sulfotransferase 1	hs6st1	hypogonadotropic hypogonadism 15 with or without anosmia
548703	carbohydrate (chondroitin 4) sulfotransferase 12	chst12	hypertension
548887	UDP-glucose ceramide glucosyltransferase	ugcg	hypertension
100488466	polypeptide N-acetylgalactosaminyltransferase 3	galnt3	hyperphosphatemic familial tumoral calcinosis
100380028	phosphatidylinositol glycan anchor biosynthesis class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
100145208	beta-1,4-N-acetyl-galactosaminyl transferase 1	b4galnt1	hereditary spastic paraplegia 26
493398	exostosin like glycosyltransferase 3	extl3	hereditary multiple exostoses
100151709	exostosin glycosyltransferase 2	ext2	hereditary multiple exostoses
100489739	heparan sulfate-glucosamine 3-sulfotransferase 6	hs3st6	hereditary angioedema
734090	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
594943	polypeptide N-acetylgalactosaminyltransferase 1	galnt1	heart valve disease
394883	glycogenin 1	gyg1	glycogen storage disease XV glycogen storage disease
448549	regucalcin	rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
100145573	transmembrane and tetratricopeptide repeat containing 3	tmtc3	epilepsy lissencephaly 8
100145711	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
549862	ALG13, UDP-N-acetylglucosaminyltransferase subunit-like	alg13l	developmental and epileptic encephalopathy 36
100379745	ALG14, UDP-N-acetylglucosaminyltransferase subunit	alg14	congenital myasthenic syndrome 15
496628	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
496641	beta-1,3-N-acetylgalactosaminyltransferase 2	b3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
100493854	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase like	mgat2l	congenital disorder of glycosylation type IIa
448439	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase	mgat2	congenital disorder of glycosylation type IIa
100488284	polypeptide N-acetylgalactosaminyltransferase 2	galnt2	congenital disorder of glycosylation type II
448472	ALG5, dolichyl-phosphate beta-glucosyltransferase	alg5	congenital disorder of glycosylation type I polycystic kidney disease

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