GlyCosmos Portal

Displaying entries **426 - 450** of **662** in total

« First

‹ Prev

…

14

15

16

17

18

19

20

21

22

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
83398	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
83921	cell migration inducing hyaluronidase 2	Cemip2
93961	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5	B3galt5	pancreatic cancer
94181	N-acetylneuraminic acid synthase (sialic acid synthase)	Nans	spondyloepimetaphyseal dysplasia, Genevieve-type
94192	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	autoimmune disease of blood
94215	UDP glucuronosyltransferase 2 family, polypeptide A1	Ugt2a1
94284	UDP glucuronosyltransferase 1 family, polypeptide A6A	Ugt1a6a	hepatitis B type 2 diabetes mellitus
97440	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9	B3gnt9
97884	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
98388	carbohydrate sulfotransferase 10	Chst10
98660	ATPase, Na+/K+ transporting, alpha 2 polypeptide	Atp1a2	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
99011	protein-O-mannosyltransferase 1	Pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
99929	TCDD-inducible poly(ADP-ribose) polymerase	Tiparp
100198	hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)	H6pd	cortisone reductase deficiency 1 cortisone reductase deficiency multiple sclerosis
100206	ADP-ribosylserine hydrolase	Adprs	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
100340	sphingomyelin phosphodiesterase, acid-like 3B	Smpdl3b
100559	UDP glucuronosyltransferase 2 family, polypeptide B38	Ugt2b38
100727	UDP glucuronosyltransferase 2 family, polypeptide B34	Ugt2b34
100910	chondroitin polymerizing factor 2	Chpf2
101187	poly (ADP-ribose) polymerase family, member 11	Parp11
101351	EGF domain specific O-linked N-acetylglucosamine transferase	Eogt	Adams-Oliver syndrome
102093	phosphorylase kinase beta	Phkb	glycogen storage disease IXb
102448	xylulokinase homolog (H. influenzae)	Xylb
102580	ALG9 alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
103534	mannoside acetylglucosaminyltransferase 4, isoenzyme B	Mgat4b

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements