GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1926 - 1950** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A1X9I601	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8TAG5	V-set and transmembrane domain-containing protein 2A	VSTM2A VSTM2	Homo sapiens (human)	2	0
D7NR06	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A060VHI0	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q8NGS0	Olfactory receptor 1N1	OR1N1 OR1N3	Homo sapiens (human)	1	0
Q8WYK1	Contactin-associated protein-like 5	CNTNAP5 CASPR5	Homo sapiens (human)	5	0
A0A0U5Q247	HLA class II histocompatibility antigen, DQ beta 1 chain	HLA-DQB1	Homo sapiens (human)	1	0
Q02790	Peptidyl-prolyl cis-trans isomerase FKBP4	FKBP4 FKBP52	Homo sapiens (human)	3	1
O75586	Mediator of RNA polymerase II transcription subunit 6	MED6 ARC33	Homo sapiens (human)	0	1
A0A2X0RQB7	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9UI42	Carboxypeptidase A4	CPA4 CPA3	Homo sapiens (human)	1	4
Q01650	Large neutral amino acids transporter small subunit 1	SLC7A5 CD98LC LAT1 MPE16	Homo sapiens (human)	0	1
E3SWL5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
M9P959	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q6ISU1	Pre T-cell antigen receptor alpha	PTCRA	Homo sapiens (human)	1	0
Q8TE49	OTU domain-containing protein 7A	OTUD7A C15orf16 CEZANNE2 OTUD7	Homo sapiens (human)	1	1
P43304	Glycerol-3-phosphate dehydrogenase, mitochondrial	GPD2	Homo sapiens (human)	2	1	cancer central nervous system cancer citrullinemia communication disorder diabetes mellitus embryoma esophagus squamous cell carcinoma gliosarcoma high grade glioma insulinoma intellectual disability intrahepatic cholestasis language disorder learning disability mixed glioma motion sickness myopia osteoporosis reflex sympathetic dystrophy thyroid adenoma thyroid cancer thyroid gland carcinoma type 2 diabetes mellitus
Q9UK23	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA	Homo sapiens (human)	6	2	Fabry disease alexia chylomicron retention disease dyslexia glycoproteinosis lipid storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis III mucopolysaccharidosis type IIIB neurodegenerative disease stuttering
P10827	Thyroid hormone receptor alpha	THRA EAR7 ERBA1 NR1A1 THRA1 THRA2	Homo sapiens (human)	0	1
Q5U5X0	Complex III assembly factor LYRM7	LYRM7 C5orf31 MZM1L	Homo sapiens (human)	0	1
E9PK86	Serpin family H member 1 (Fragment)	SERPINH1	Homo sapiens (human)	2	0
P20933	N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase	AGA	Homo sapiens (human)	4	11	Clostridium difficile colitis Down syndrome Fabry disease Klippel-Feil syndrome Laron syndrome abdominal obesity-metabolic syndrome 1 achalasia achondroplasia acne acrodermatitis agranulocytosis alcoholic hepatitis allergic bronchopulmonary aspergillosis alopecia androgenic alopecia arthritis arthropathy aspartylglucosaminuria attention deficit hyperactivity disorder cancer cataract celiac disease cerebral degeneration cervical squamous cell carcinoma cholecystitis chylomicron retention disease clubfoot common wart congenital disorder of glycosylation craniosynostosis dental caries dentin caries dermatitis herpetiformis diabetes mellitus diabetic ketoacidosis diarrhea dystonia encephalitis encephalomyelitis enterocele eosinophilic esophagitis epilepsy esophageal disease familial isolated hypoparathyroidism fucosidosis functional diarrhea gestational diabetes gingival hypertrophy gingival overgrowth goiter hepatitis C hepatocellular carcinoma hypoparathyroidism immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza inguinal hernia intellectual disability irritable bowel syndrome learning disability lingual-facial-buccal dyskinesia lipid storage disease livedoid vasculitis liver cancer liver cirrhosis lupus nephritis lysosomal storage disease megaesophagus microcephaly mitral valve insufficiency mitral valve prolapse mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis neurocirculatory asthenia neutropenia obsolete dyspepsia obsolete type 1 diabetes mellitus 9 omphalocele otitis media peroxisome biogenesis disorder 10A placental insufficiency primary sclerosing cholangitis schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis scoliosis selective IgA deficiency disease severe congenital neutropenia skeletal tuberculosis speech disorder spondylolisthesis spondylolysis stomach cancer stomach carcinoma stomach disease thyroid gland disease tropical sprue tuberculosis 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 ulcerative colitis umbilical hernia vascular skin disease visual epilepsy
Q14952	Killer cell immunoglobulin-like receptor 2DS3	KIR2DS3 NKAT7	Homo sapiens (human)	3	0
Q01085	Nucleolysin TIAR	TIAL1	Homo sapiens (human)	2	1
Q13614	Myotubularin-related protein 2	MTMR2 KIAA1073	Homo sapiens (human)	0	1	Bell's palsy Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease agenesis of the corpus callosum with peripheral neuropathy agnosia axonal neuropathy cancer centronuclear myopathy X-linked centronuclear myopathy clubfoot congenital structural myopathy demyelinating polyneuropathy developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis glaucoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 motor peripheral neuropathy myopathy neurodegenerative disease neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy scoliosis sensory peripheral neuropathy stomach cancer stomach carcinoma

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