GlyCosmos Portal

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Displaying entries **115151 - 115175** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q11206	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 4	ST3GAL4 CGS23 NANTA3 SIAT4C STZ	Homo sapiens (human)	5	4	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
Q41438	3-hydroxy-3-methylglutaryl-coenzyme A reductase 3	HMG3	Solanum tuberosum (potato)	5	0
Q9FH06	Serine carboxypeptidase-like 41	SCPL41	Arabidopsis thaliana (thale cress)	5	0
Q92615	La-related protein 4B	LARP4B KIAA0217 LARP5	Homo sapiens (human)	5	1
Q7RYY1	Putative lipase atg15	atg15	Neurospora crassa OR74A	5	0
Q14833	Metabotropic glutamate receptor 4	GRM4 GPRC1D MGLUR4	Homo sapiens (human)	5	0
Q1PHM6	Envelope glycoprotein gp160	env	Human immunodeficiency virus 1	5	0
A8MTB9	Carcinoembryonic antigen-related cell adhesion molecule 18	CEACAM18	Homo sapiens (human)	5	1
Q12889	Oviduct-specific glycoprotein	OVGP1 MUC9 OGP	Homo sapiens (human)	5	1	bagassosis cancer centronuclear myopathy ciliary body disease colorectal cancer colorectal carcinoma congenital structural myopathy embryoma endometrial carcinoma endosalpingiosis iris disease large intestine cancer laryngitis ovarian cancer ovarian carcinoma panuveitis transient myeloproliferative syndrome tubular aggregate myopathy 1 uveitis
Q06BH3	Protein STRUBBELIG-RECEPTOR FAMILY 1	SRF1	Arabidopsis thaliana (thale cress)	5	0
Q92547	DNA topoisomerase 2-binding protein 1	TOPBP1 KIAA0259	Homo sapiens (human)	5	3
A6X8Z5	Rho GTPase-activating protein 31	Arhgap31 Cdgap Kiaa1204	Mus musculus (house mouse)	5	4
A0A7J8CZ72	Angiotensin-converting enzyme	HJG59_009457	Molossus molossus (Pallas's mastiff bat)	5	0
Q9LXX4	bZIP transcription factor 49	BZIP49	Arabidopsis thaliana (thale cress)	5	0
Q9R0I7	YLP motif-containing protein 1	Ylpm1 Zap Zap3	Mus musculus (house mouse)	5	4
Q86WK7	Amphoterin-induced protein 3	AMIGO3 ALI3 KIAA1851	Homo sapiens (human)	5	2
P68328	Envelope glycoprotein E	gE	Equine herpesvirus type 1 (strain AB1)	5	0
P55025	Tyrosinase	tyr tyro	Oryzias latipes (Japanese medaka)	5	0
Q8H1R2	Probable inactive purple acid phosphatase 24	PAP24	Arabidopsis thaliana (thale cress)	5	0
P28693	Ephrin type-B receptor 2	EPHB2 CEK5	Gallus gallus (chicken)	5	0
P08483	Muscarinic acetylcholine receptor M3	Chrm3 Chrm-3	Rattus norvegicus (Norway rat)	5	0
Q0UHZ9	Fasciclin-like arabinogalactan protein elcF	elcF	Parastagonospora nodorum SN15	5	0
P08962	CD63 antigen	CD63 MLA1 TSPAN30	Homo sapiens (human)	5	111
Q29477	Lactotransferrin	LTF	Capra hircus (goat)	5	0
Q14CZ8	Hepatic and glial cell adhesion molecule	HEPACAM	Homo sapiens (human)	5	1

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