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
404232	carbohydrate (chondroitin 4) sulfotransferase 11	chst11
404633	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2	b3galt2
404732	carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14	chst14	Ehlers-Danlos syndrome musculocontractural type 1
405766	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2a	b3gnt2a
406367	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	gapdhs	Alzheimer's disease
406477	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 6 (GalNAc-T6)	galnt6
406567	FGGY carbohydrate kinase domain containing	fggy
406731	UDP glucuronosyltransferase 1 family a, b	ugt1ab	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
406831	glycogenin 1a	gyg1a	glycogen storage disease XV glycogen storage disease
407076	carbohydrate (chondroitin 4) sulfotransferase 12a	chst12a	hypertension
407614	ALG11 alpha-1,2-mannosyltransferase	alg11	congenital disorder of glycosylation Ip
407623	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7, like	b3gnt7l
407659	ST3 beta-galactoside alpha-2,3-sialyltransferase 3b	st3gal3b	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
407706	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase	st6galnac
407715	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	st6galnac6
407716	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5b	st6galnac5b
414848	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	rfng
415152	glycogenin 1b	gyg1b	glycogen storage disease XV glycogen storage disease
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
431727	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	mgat4b
436733	zgc:92907	zgc:92907
445022	xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I)	b4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
445060	beta-1,3-glucuronyltransferase 2 (glucuronosyltransferase S)	b3gat2	Barrett's esophagus schizophrenia
445124	carbohydrate (keratan sulfate Gal-6) sulfotransferase 1	chst1
445202	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I

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