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 **1 - 25** of **17989** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
175	aspartylglucosaminidase	AGA Aliases: ASRG N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase glycosylasparaginase	Homo sapiens (human)	aspartylglucosaminuria lysosomal storage disease
433	asialoglycoprotein receptor 2	ASGR2 Aliases: CLEC4H2	Homo sapiens (human)
538	ATPase copper transporting alpha	ATP7A	Homo sapiens (human)	Menkes disease X-linked distal spinal muscular atrophy 3 cutis laxa occipital horn syndrome
650	bone morphogenetic protein 2	BMP2	Homo sapiens (human)	brachydactyly type A2 hemochromatosis type 1 osteoarthritis osteoporosis otosclerosis prostate cancer short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 tooth agenesis
658	bone morphogenetic protein receptor type 1B	BMPR1B	Homo sapiens (human)	acromesomelic dysplasia 3 brachydactyly type A1D brachydactyly type A2 osteochondrodysplasia
659	bone morphogenetic protein receptor type 2	BMPR2	Homo sapiens (human)	heart septal defect primary pulmonary hypertension pulmonary hypertension pulmonary venoocclusive disease 1
695	Bruton tyrosine kinase	BTK	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma X-linked agammaglobulinemia agammaglobulinemia central nervous system lymphoma isolated growth hormone deficiency type III mantle cell lymphoma
1280	collagen type II alpha 1 chain	COL2A1	Homo sapiens (human)	Kniest dysplasia Legg-Calve-Perthes disease Stickler syndrome 1 Stickler syndrome Torrance type platyspondylic dysplasia achondrogenesis type II chondrosarcoma chorioretinitis cleft palate eye disease multiple epiphyseal dysplasia with myopia and deafness myopia osteoarthritis osteochondrodysplasia osteonecrosis retinal detachment spondyloarthropathy spondyloepimetaphyseal dysplasia, Strudwick type spondyloepiphyseal dysplasia Stanescu type spondyloepiphyseal dysplasia congenita spondyloperipheral dysplasia
1301	collagen type XI alpha 1 chain	COL11A1	Homo sapiens (human)	Marshall syndrome Stickler syndrome 2 autosomal dominant nonsyndromic deafness 37 fibrochondrogenesis 1
1514	cathepsin L	CTSL	Homo sapiens (human)	hypertrophic cardiomyopathy
1990	chymotrypsin like elastase 1	CELA1	Homo sapiens (human)
2131	exostosin glycosyltransferase 1	EXT1 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase ttv	Homo sapiens (human)	chondrosarcoma hereditary multiple exostoses
2132	exostosin glycosyltransferase 2	EXT2 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase SOTV	Homo sapiens (human)
2134	exostosin like glycosyltransferase 1	EXTL1 Aliases: EXTL MGC70794 alpha-N-acetylglucosaminyltransferase II exostosin-L glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase glucuronyl-N-acetylglucosaminylproteoglycan alpha-1,4-N- acetylglucosaminyltransferase	Homo sapiens (human)
2135	exostosin like glycosyltransferase 2	EXTL2 Aliases: alpha-1,4-N-acteylhexosaminyltransferase	Homo sapiens (human)
2137	exostosin like glycosyltransferase 3	EXTL3 Aliases: REG receptor REGR botv glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase	Homo sapiens (human)
2530	fucosyltransferase 8	FUT8 Aliases: alpha (1,6) fucosyltransferase	Homo sapiens (human)
2595	glucosidase alpha, neutral C	GANC	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)
2720	galactosidase beta 1	GLB1 Aliases: EBP elastin binding protein	Homo sapiens (human)	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis type IVB
2799	glucosamine (N-acetyl)-6-sulfatase	GNS Aliases: N-acetylglucosamine-6-sulfatase Sanfilippo disease IIID	Homo sapiens (human)	mucopolysaccharidosis III mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID
2817	glypican 1	GPC1 Aliases: glypican glypican proteoglycan 1	Homo sapiens (human)
2990	glucuronidase beta	GUSB	Homo sapiens (human)	mucopolysaccharidosis type VII
3073	hexosaminidase subunit alpha	HEXA Aliases: GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha	Homo sapiens (human)	Tay-Sachs disease
3074	hexosaminidase subunit beta	HEXB Aliases: beta-hexosaminidase subunit beta	Homo sapiens (human)	Sandhoff disease spinal muscular atrophy

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