GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **276 - 300** of **358** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
447881	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1, like 3	gbgt1l3	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
446214	LARGE xylosyl- and glucuronyltransferase 2	large2
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
445562	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	st3gal2
445376	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1	st6gal1	alcohol use disorder high grade glioma
445327	ALG6 alpha-1,3-glucosyltransferase	alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
445322	carbohydrate sulfotransferase 10	chst10
445202	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
445124	carbohydrate (keratan sulfate Gal-6) sulfotransferase 1	chst1
445060	beta-1,3-glucuronyltransferase 2 (glucuronosyltransferase S)	b3gat2	Barrett's esophagus schizophrenia
445022	xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I)	b4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
436733	zgc:92907	zgc:92907
431727	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	mgat4b
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
415152	glycogenin 1b	gyg1b	glycogen storage disease XV glycogen storage disease
414848	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	rfng
407716	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5b	st6galnac5b
407715	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	st6galnac6
407706	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase	st6galnac
407659	ST3 beta-galactoside alpha-2,3-sialyltransferase 3b	st3gal3b	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
407623	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7, like	b3gnt7l
407614	ALG11 alpha-1,2-mannosyltransferase	alg11	congenital disorder of glycosylation Ip
407076	carbohydrate (chondroitin 4) sulfotransferase 12a	chst12a	hypertension
406831	glycogenin 1a	gyg1a	glycogen storage disease XV glycogen storage disease

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