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 **1376 - 1400** 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
A0A2R8YD45	Tripeptidyl peptidase 1	TPP1	Homo sapiens (human)	1	0
O15016	Tripartite motif-containing protein 66	TRIM66 C11orf29 KIAA0298	Homo sapiens (human)	1	1
Q9BYV6	Tripartite motif-containing protein 55	TRIM55 MURF2 RNF29	Homo sapiens (human)	1	1
Q14134	Tripartite motif-containing protein 29	TRIM29 ATDC	Homo sapiens (human)	4	1
O95361	Tripartite motif-containing protein 16	TRIM16 EBBP	Homo sapiens (human)	0	1
P60174	Triosephosphate isomerase	TPI1 TPI	Homo sapiens (human)	2	3	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 Behcet's disease Chagas disease Creutzfeldt-Jakob disease Ebola hemorrhagic fever Goodpasture syndrome Japanese encephalitis Pick's disease Reye syndrome Takayasu's arteritis adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aseptic meningitis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bipolar disorder blastomycosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy central nervous system cancer central nervous system disease cerebral degeneration cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chronic fatigue syndrome chronic myeloid leukemia colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia congestive heart failure coronary artery disease cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia dengue disease dermatitis diaphragm disease diarrhea disease of metabolism dystonia embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma exanthem familial hypertrophic cardiomyopathy familial periodic paralysis favism giant cell glioblastoma giardiasis glioblastoma gliosarcoma granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypertrophic cardiomyopathy immune system disease inherited metabolic disorder intellectual disability intrinsic asthma kwashiorkor large intestine cancer learning disability leech infestation lingual-facial-buccal dyskinesia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma malignant pleural mesothelioma marasmus melanoma microsporidiosis mixed glioma multiple sclerosis myelitis myiasis myopathy nervous system disease neuroblastoma neuromuscular disease neuropathy newborn respiratory distress syndrome nodular goiter normocytic anemia nutrition disease ocular hypertension osteoarthritis osteochondritis dissecans osteoporosis papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis peripheral nervous system disease periventricular leukomalacia pleurisy polyarteritis nodosa polyneuropathy progressive supranuclear palsy proliferative type fibrocystic change of breast protein-energy malnutrition reflex sympathetic dystrophy rheumatoid arthritis schizophrenia scleroderma skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma systemic lupus erythematosus systemic scleroderma thyroid gland papillary carcinoma tongue squamous cell carcinoma toxoplasmosis triosephosphate isomerase deficiency trypanosomiasis tuberculosis tubular adenocarcinoma uveal melanoma viral infectious disease viral meningitis visual epilepsy yellow fever
Q3LXA3	Triokinase/FMN cyclase	TKFC DAK	Homo sapiens (human)	0	1	cataract diabetes mellitus diabetic ketoacidosis liver disease type 2 diabetes mellitus
Q9HCJ0	Trinucleotide repeat-containing gene 6C protein	TNRC6C KIAA1582	Homo sapiens (human)	13	2
Q9UPQ9	Trinucleotide repeat-containing gene 6B protein	TNRC6B KIAA1093	Homo sapiens (human)	9	5
Q8NDV7	Trinucleotide repeat-containing gene 6A protein	TNRC6A CAGH26 KIAA1460 TNRC6	Homo sapiens (human)	22	5
O15417	Trinucleotide repeat-containing gene 18 protein	TNRC18 CAGL79 KIAA1856	Homo sapiens (human)	3	1
Q9NZC2	Triggering receptor expressed on myeloid cells 2	TREM2	Homo sapiens (human)	2	0
Q9NP99	Triggering receptor expressed on myeloid cells 1	TREM1	Homo sapiens (human)	3	0
P22102	Trifunctional purine biosynthetic protein adenosine-3	GART PGFT PRGS	Homo sapiens (human)	0	1
P55084	Trifunctional enzyme subunit beta, mitochondrial	HADHB	Homo sapiens (human)	0	1	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 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 Norum disease Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia beta-ketothiolase deficiency breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease cholestasis choreaacanthocytosis clubfoot colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure critical illness polyneuropathy developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endomyocardial fibrosis epilepsy familial hyperlipidemia familial periodic paralysis fibromyalgia fundus albipunctatus heart disease hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hypercalcemia hypertrophic cardiomyopathy hypolipoproteinemia hypoparathyroidism inflammatory and toxic neuropathy intellectual disability lactic acidosis large intestine cancer learning disability melanoma meningoencephalitis mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse motor peripheral neuropathy myoglobinuria myopathy myositis nephrocalcinosis neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease phosphorus metabolism disease placental insufficiency polydactyly polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinitis pigmentosa sick sinus syndrome skin melanoma steatotic liver disease tricuspid valve insufficiency urea cycle disorder visual epilepsy
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	Homo sapiens (human)	4	4	Barth syndrome HELLP syndrome Norum disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia acquired immunodeficiency syndrome adult respiratory distress syndrome agnosia alpha 1-antitrypsin deficiency alternating exotropia amyotrophic lateral sclerosis arthritis arthropathy blindness breast cancer bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease cholestasis choreaacanthocytosis clubfoot cone-rod dystrophy congenital adrenal hyperplasia congenital stationary night blindness 1A congenital stationary night blindness congestive heart failure coronary artery disease cystinuria cytochrome-c oxidase deficiency disease developmental coordination disorder diabetes mellitus dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism endomyocardial fibrosis epilepsy exotropia familial hypertrophic cardiomyopathy familial periodic paralysis fibromyalgia fundus albipunctatus galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemophagocytic lymphohistiocytosis hepatitis C human immunodeficiency virus infectious disease hypercalcemia hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia hypoparathyroidism inflammatory bowel disease inherited metabolic disorder intellectual disability lactic acidosis learning disability liver disease lung benign neoplasm lung cancer lung carcinoma metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse monocular exotropia myoglobinuria myopathy myopia myositis nephrocalcinosis neuropathy newborn respiratory distress syndrome night blindness obesity obsolete asthenopia osteoarthritis peripheral nervous system disease phosphorus metabolism disease placental insufficiency polyneuropathy pre-eclampsia progressive muscular atrophy prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinal disease retinitis pigmentosa retinitis sick sinus syndrome staphyloma posticum steatotic liver disease sudden infant death syndrome tricuspid valve insufficiency type 2 diabetes mellitus urea cycle disorder visual epilepsy von Willebrand's disease 2 von Willebrand's disease
Q5QJ38	Trichohyalin-like protein 1	TCHHL1 S100A17 THHL1	Homo sapiens (human)	2	1
Q07283	Trichohyalin	TCHH THH THL TRHY	Homo sapiens (human)	0	1
P53007	Tricarboxylate transport protein, mitochondrial	SLC25A1 SLC20A3	Homo sapiens (human)	0	1
Q96RU7	Tribbles homolog 3	TRIB3 C20orf97 NIPK SKIP3 TRB3	Homo sapiens (human)	0	1
Q92519	Tribbles homolog 2	TRIB2 TRB2	Homo sapiens (human)	0	1
Q96RU8	Tribbles homolog 1	TRIB1 C8FW GIG2 TRB1	Homo sapiens (human)	0	1
Q13061	Triadin	TRDN	Homo sapiens (human)	3	2
Q7Z2Z1	Treslin	TICRR C15orf42	Homo sapiens (human)	0	1
Q6UXN2	Trem-like transcript 4 protein	TREML4 TLT4	Homo sapiens (human)	1	0

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