GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (358) Glycans (175) Glycoproteins (592) Lectins (18) Pathways (252)

Displaying entries **51 - 75** of **358** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
557181	ALG13 UDP-N-acetylglucosaminyltransferase subunit	alg13	developmental and epileptic encephalopathy 36
450072	ALG14 UDP-N-acetylglucosaminyltransferase subunit	alg14	congenital myasthenic syndrome 15
497644	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
446213	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
492773	protein O-mannose kinase	pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
553716	beta-1,3-N-acetylgalactosaminyltransferase 2	b3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
100000478	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	mgat2	congenital disorder of glycosylation type IIa
570248	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2	galnt2	congenital disorder of glycosylation type II
266797	STT3 oligosaccharyltransferase complex catalytic subunit A	stt3a	congenital disorder of glycosylation Iw
323918	STT3 oligosaccharyltransferase complex catalytic subunit B	stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
407614	ALG11 alpha-1,2-mannosyltransferase	alg11	congenital disorder of glycosylation Ip
393598	ALG9 alpha-1,2-mannosyltransferase	alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
334161	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
566539	dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)	dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
403068	ALG2 alpha-1,3/1,6-mannosyltransferase	alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
327601	ALG8 alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
569494	ALG12 alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
445202	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
553725	ALG3 alpha-1,3- mannosyltransferase	alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
445327	ALG6 alpha-1,3-glucosyltransferase	alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
559736	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 12	galnt12	colorectal cancer
571246	heparan sulfate (glucosamine) 3-O-sulfotransferase 2	hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
565316	diacylglycerol O-acyltransferase 2	dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease

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