GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P63096	Guanine nucleotide-binding protein G(i) subunit alpha-1	GNAI1	1	2
P04899	Guanine nucleotide-binding protein G(i) subunit alpha-2	GNAI2 GNAI2B	5	2
P08754	Guanine nucleotide-binding protein G(i) subunit alpha-3	GNAI3	4	1
P63092	Guanine nucleotide-binding protein G(s) subunit alpha isoforms short	GNAS GNAS1 GSP	0	1
Q5JWF2	Guanine nucleotide-binding protein G(s) subunit alpha isoforms XLas	GNAS GNAS1	0	1
O95467	Neuroendocrine secretory protein 55	GNAS GNAS1	0	1
P84996	Protein ALEX	GNAS GNAS1	0	1
A8MTJ3	Guanine nucleotide-binding protein G(t) subunit alpha-3	GNAT3	2	1
P62873	Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1	GNB1	2	1
Q9BYB4	Guanine nucleotide-binding protein subunit beta-like protein 1	GNB1L GY2 KIAA1645 WDR14	0	1
P62879	Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2	GNB2	0	1
Q9HAV0	Guanine nucleotide-binding protein subunit beta-4	GNB4	1	1
O14775	Guanine nucleotide-binding protein subunit beta-5	GNB5	0	1
P63218	Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5	GNG5 GNGT5	0	1
P36915	Guanine nucleotide-binding protein-like 1	GNL1 HSR1	0	1
Q13823	Nucleolar GTP-binding protein 2	GNL2 NGP1	2	1
Q9BVP2	Guanine nucleotide-binding protein-like 3	GNL3 E2IG3 NS	1	1
Q9NVN8	Guanine nucleotide-binding protein-like 3-like protein	GNL3L	0	1
O15228	Dihydroxyacetone phosphate acyltransferase	GNPAT DAPAT DHAPAT	0	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
P46926	Glucosamine-6-phosphate isomerase 1	GNPDA1 GNPI HLN KIAA0060	0	1
Q8TDQ7	Glucosamine-6-phosphate isomerase 2	GNPDA2 GNP2	0	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 allergic asthma asthma cardiovascular system disease cerebral degeneration diabetes mellitus essential hypertension heart disease hypertension intrinsic asthma obesity type 2 diabetes mellitus
Q96EK6	Glucosamine 6-phosphate N-acetyltransferase	GNPNAT1 GNA1	0	1	diabetes mellitus diabetic ketoacidosis type 2 diabetes mellitus
Q3T906	N-acetylglucosamine-1-phosphotransferase subunits alpha/beta	GNPTAB GNPTA KIAA1208	42	24	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
Q9UJJ9	N-acetylglucosamine-1-phosphotransferase subunit gamma	GNPTG C16orf27 GNPTAG	11	20	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
P30968	Gonadotropin-releasing hormone receptor	GNRHR GRHR	2	0

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