GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **226 - 250** of **358** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
497615	fucosyltransferase 10	fut10
447896	fucose mutarotase	fuom
792063	alpha(1,3)fucosyltransferase gene 2	ft2	candidiasis
768121	forkhead box O1 a	foxo1a	Parkinson's disease alveolar rhabdomyosarcoma congestive heart failure hepatocellular carcinoma metabolic dysfunction-associated steatotic liver disease prostate cancer
100006345	fukutin	fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
571426	fukutin related protein	fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
406567	FGGY carbohydrate kinase domain containing	fggy
493783	exostosin-like glycosyltransferase 3	extl3	hereditary multiple exostoses
558373	exostosin-like glycosyltransferase 2	extl2
493780	exostosin glycosyltransferase 2	ext2	hereditary multiple exostoses
497281	exostoses (multiple) 1c	ext1c	hereditary multiple exostoses
497280	exostosin glycosyltransferase 1b	ext1b	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
497279	exostosin glycosyltransferase 1a	ext1a	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
798087	EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase	eogt	Adams-Oliver syndrome
558487	enolase 4	eno4
561239	endo-beta-N-acetylglucosaminidase	engase
796987	dpy-19 like C-mannosyltransferase 3	dpy19l3
368327	dpy-19-like 1, like (H. sapiens)	dpy19l1l	spermatogenic failure 9
445202	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
566539	dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)	dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
561810	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	dnph1
494076	dehydrogenase E1 and transketolase domain containing 1	dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
449558	dihydrodiol dehydrogenase, tandem duplicate 2	dhdh.2
565316	diacylglycerol O-acyltransferase 2	dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
560826	chondroitin sulfate N-acetylgalactosaminyltransferase 2	csgalnact2

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