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 **13176 - 13200** 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
E9PNM3	Fibroblast growth factor receptor 1 (Fragment)	FGFR1	Homo sapiens (human)	2	0
Q30069	MHC class II HLA-DQ-alpha chain (Fragment)	HLA-DQA1	Homo sapiens (human)	2	0
Q3KQV9	UDP-N-acetylhexosamine pyrophosphorylase-like protein 1	UAP1L1	Homo sapiens (human)	2	1	hepatocellular carcinoma liver cancer
Q8NCC5	Sugar phosphate exchanger 3	SLC37A3 SPX3	Homo sapiens (human)	2	0
Q8WVQ1	Soluble calcium-activated nucleotidase 1	CANT1 SHAPY	Homo sapiens (human)	2	5
Q9Y3A3	MOB-like protein phocein	MOB4 MOB3 MOBKL3 PHOCN PREI3	Homo sapiens (human)	2	1
Q8N2Y8	AP-4 complex accessory subunit RUSC2	RUSC2 KIAA0375	Homo sapiens (human)	2	1
Q86VF5	2-acylglycerol O-acyltransferase 3	MOGAT3 DC7 DGAT2L7	Homo sapiens (human)	2	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 cerebral degeneration steatotic liver disease
P98153	Integral membrane protein DGCR2/IDD	DGCR2 IDD KIAA0163	Homo sapiens (human)	2	4	Bannayan-Riley-Ruvalcaba syndrome Baraitser-Winter syndrome Cowden syndrome DiGeorge syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Nezelof syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia acromegaly acute myocardial infarction adrenal gland cancer amyloidosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bipolar disorder blepharophimosis branchiootic syndrome cancer cervix disease chronic interstitial cystitis congenital heart disease coronary thrombosis craniosynostosis degenerative disc disease delusional disorder diabetes mellitus diabetic ketoacidosis double outlet right ventricle duodenum cancer embryoma epilepsy heart cancer hyperpituitarism hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism immune system disease intellectual disability interstitial cystitis learning disability microcephaly myocardial infarction myotonic dystrophy type 1 neuroblastoma obsolete type 1 diabetes mellitus 9 orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia pheochromocytoma primary biliary cholangitis prune belly syndrome pseudohypoparathyroidism schizophrenia silent myocardial infarction small intestine cancer 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 velocardiofacial syndrome ventricular septal defect visual epilepsy
Q07108	Early activation antigen CD69	CD69 CLEC2C	Homo sapiens (human)	2	3
P09486	SPARC	SPARC ON	Homo sapiens (human)	2	71
Q8NE01	Metal transporter CNNM3	CNNM3 ACDP3	Homo sapiens (human)	2	2
Q9Y6F9	Protein Wnt-6	WNT6	Homo sapiens (human)	2	0
P52566	Rho GDP-dissociation inhibitor 2	ARHGDIB GDIA2 GDID4 RAP1GN1	Homo sapiens (human)	2	1
P23368	NAD-dependent malic enzyme, mitochondrial	ME2	Homo sapiens (human)	2	1	bipolar disorder cancer embryoma epilepsy generalized epilepsy with febrile seizures plus giant cell glioblastoma glioblastoma high grade glioma idiopathic generalized epilepsy leukemia lung benign neoplasm lung cancer lung non-small cell carcinoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder
Q96JJ7	Protein disulfide-isomerase TMX3	TMX3 KIAA1830 TXNDC10	Homo sapiens (human)	2	10
Q12809	Potassium voltage-gated channel subfamily H member 2	KCNH2 ERG ERG1 HERG	Homo sapiens (human)	2	0
Q99460	26S proteasome non-ATPase regulatory subunit 1	PSMD1	Homo sapiens (human)	2	2
Q00587	Cdc42 effector protein 1	CDC42EP1 BORG5 CEP1 MSE55	Homo sapiens (human)	2	1
P50616	Protein Tob1	TOB1 TOB TROB1	Homo sapiens (human)	2	1
H7C543	CD166 antigen (Fragment)	ALCAM	Homo sapiens (human)	2	0
Q92819	Hyaluronan synthase 2	HAS2	Homo sapiens (human)	2	1	Barrett's esophagus Down syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma allergic asthma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer childhood cerebral astrocytoma childhood osteosarcoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital heart disease coronary artery disease cribriform carcinoma diabetes insipidus diabetes mellitus diabetic ketoacidosis embryoma endocrine exophthalmos enophthalmos essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma gliosarcoma glomerulonephritis granular cell carcinoma high grade glioma hyperglycemia hyperuricemia idiopathic interstitial pneumonia intrinsic asthma juvenile pilocytic astrocytoma kidney disease large intestine cancer leukoencephalopathy with vanishing white matter liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacytic lymphoma macroglobulinemia malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mixed glioma multiple myeloma myelodysplastic syndrome myopia myotonic dystrophy type 1 nephritis nephrosis neurohypophyseal diabetes insipidus obesity obsolete Matthew-Wood syndrome obsolete exophthalmos obsolete lymphoplasmacytic lymphoma orbital disease osteosarcoma pilocytic astrocytoma placental insufficiency polycystic ovary syndrome postinflammatory pulmonary fibrosis primary open angle glaucoma primary pulmonary hypertension protoplasmic astrocytoma pulmonary fibrosis pulmonary hypertension pyoureter sarcomatoid carcinoma skin melanoma squamous cell carcinoma subependymal giant cell astrocytoma tetralogy of Fallot tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer ventricular septal defect
X5DNK3	Receptor tyrosine-protein kinase erbB-2 (Fragment)	ERBB2	Homo sapiens (human)	2	0
Q8IUB9	Keratin-associated protein 19-1	KRTAP19-1 KAP19.1 KRTAP19.1	Homo sapiens (human)	2	1
P30086	Phosphatidylethanolamine-binding protein 1	PEBP1 PBP PEBP	Homo sapiens (human)	2	2

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