GlyCosmos Portal

Displaying entries **126 - 150** of **358** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
797512	fucosyltransferase 8a (alpha (1,6) fucosyltransferase)	fut8a	pulmonary emphysema
562250	fucosyltransferase 7 (alpha (1,3) fucosyltransferase)	fut7	candidiasis
568888	fucosyltransferase 11 (alpha (1,3) fucosyltransferase)	fut11	stomach cancer
497615	fucosyltransferase 10	fut10
447896	fucose mutarotase	fuom
768121	forkhead box O1 a	foxo1a	Parkinson's disease alveolar rhabdomyosarcoma congestive heart failure hepatocellular carcinoma metabolic dysfunction-associated steatotic liver disease prostate cancer
493783	exostosin-like glycosyltransferase 3	extl3	hereditary multiple exostoses
558373	exostosin-like glycosyltransferase 2	extl2
101885478	exostosin-1-like	LOC101885478
493780	exostosin glycosyltransferase 2	ext2	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
497281	exostoses (multiple) 1c	ext1c	hereditary multiple exostoses
558487	enolase 4	eno4
561239	endo-beta-N-acetylglucosaminidase	engase
368327	dpy-19-like 1, like (H. sapiens)	dpy19l1l	spermatogenic failure 9
796987	dpy-19 like C-mannosyltransferase 3	dpy19l3
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
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
494076	dehydrogenase E1 and transketolase domain containing 1	dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
555344	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1a	c1galt1a	autoimmune disease of blood
337131	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like b	c1galt1lb	autoimmune disease of blood
557675	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like a	c1galt1la	autoimmune disease of blood

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