GlyCosmos Portal

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Displaying entries **1176 - 1200** of **423164** in total

« First

‹ Prev

…

44

45

46

47

48

49

50

51

52

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
2639	glutaryl-CoA dehydrogenase	GCDH Aliases: ACAD5 GCD	Homo sapiens (human)	glutaric acidemia I
2641	glucagon	GCG	Homo sapiens (human)	Alzheimer's disease prediabetes syndrome
2642	glucagon receptor	GCGR	Homo sapiens (human)	Mahvash Disease type 2 diabetes mellitus
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 permanent neonatal diabetes mellitus type 2 diabetes mellitus
2648	lysine acetyltransferase 2A	KAT2A	Homo sapiens (human)
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)
2651	glucosaminyl (N-acetyl) transferase 2 (I blood group)	GCNT2 Aliases: IGNT Ii blood group NAGCT1 ULG3 bA360O19.2 bA421M1.1 unassigned linkage group 3	Homo sapiens (human)	cataract 13 with adult i phenotype cataract
2652	opsin 1, medium wave sensitive	OPN1MW	Homo sapiens (human)	blue cone monochromacy red-green color blindness
2653	glycine cleavage system protein H	GCSH Aliases: lipoic acid-containing protein	Homo sapiens (human)	multiple mitochondrial dysfunctions syndrome
2657	growth differentiation factor 1	GDF1	Homo sapiens (human)	congenital heart disease multiple types of congenital heart defects 6 visceral heterotaxy
2658	growth differentiation factor 2	GDF2	Homo sapiens (human)	hereditary hemorrhagic telangiectasia
2660	myostatin	MSTN	Homo sapiens (human)	myostatin-related muscle hypertrophy
2661	growth differentiation factor 9	GDF9	Homo sapiens (human)	primary ovarian insufficiency 14
2662	growth differentiation factor 10	GDF10	Homo sapiens (human)
2668	glial cell derived neurotrophic factor	GDNF	Homo sapiens (human)	Hirschsprung's disease Parkinsonism anxiety disorder depressive disorder epilepsy glomerulonephritis heroin dependence
2670	glial fibrillary acidic protein	GFAP	Homo sapiens (human)	Alexander disease
2671	growth factor, augmenter of liver regeneration	GFER	Homo sapiens (human)	kidney failure renal fibrosis
2673	glutamine--fructose-6-phosphate transaminase 1	GFPT1 Aliases: GFA GFAT GFAT1	Homo sapiens (human)	congenital myasthenic syndrome 12 obesity
2674	GDNF family receptor alpha 1	GFRA1 Aliases: GDNFR GFR-ALPHA-1 RET1L RETL1 TRNR1	Homo sapiens (human)	renal agenesis
2675	GDNF family receptor alpha 2	GFRA2 Aliases: GDNFRB NTNRA RETL2 TRNR2	Homo sapiens (human)
2676	GDNF family receptor alpha 3	GFRA3	Homo sapiens (human)
2677	gamma-glutamyl carboxylase	GGCX	Homo sapiens (human)	combined deficiency of vitamin K-dependent clotting factors 1
2678	gamma-glutamyltransferase 1	GGT1	Homo sapiens (human)	gamma-glutamyl transpeptidase deficiency
2683	beta-1,4-galactosyltransferase 1	B4GALT1 Aliases: Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T1 lactose synthase A	Homo sapiens (human)	congenital disorder of glycosylation type IId congenital disorder of glycosylation
2686	gamma-glutamyltransferase 7	GGT7 Aliases: D20S101 dJ18C9.2	Homo sapiens (human)

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements