GlyCosmos Portal

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Displaying entries **13051 - 13075** 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
Q96AG4	Leucine-rich repeat-containing protein 59	LRRC59	Homo sapiens (human)	0	1
Q96AE7	Tetratricopeptide repeat protein 17	TTC17	Homo sapiens (human)	7	13
Q96AE4	Far upstream element-binding protein 1	FUBP1	Homo sapiens (human)	9	1
Q96AD5	Patatin-like phospholipase domain-containing protein 2	PNPLA2 ATGL	Homo sapiens (human)	4	2	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 Barth syndrome Chanarin-Dorfman syndrome Ehlers-Danlos syndrome Kuhnt-Junius degeneration Laron syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acanthosis nigricans achondroplasia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult liposarcoma age related macular degeneration agnosia anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive congenital ichthyosis 1 bacterial sepsis bladder carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cartilage disease cavernous hemangioma celiac disease central nervous system cancer cerebral degeneration childhood liposarcoma childhood osteosarcoma cholecystitis chorioangioma chylomicron retention disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cone-rod dystrophy congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma endometrial hyperplasia endomyocardial fibrosis epithelioid leiomyosarcoma exudative vitreoretinopathy 1 exudative vitreoretinopathy eye disease familial combined hyperlipidemia familial hyperlipidemia familial lipoprotein lipase deficiency familial periodic paralysis familial retinoblastoma fibromyalgia fundus albipunctatus gestational diabetes gliosarcoma glomus tumor glucose intolerance glycogen storage disease II granular cell carcinoma heart disease hemangioma hepatoblastoma hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperinsulinism hyperlipoproteinemia type V hypertrophic cardiomyopathy ichthyosis impotence intramuscular hemangioma isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leiomyosarcoma leukostasis lipoatrophic diabetes mellitus lipodystrophy liposarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma lymphangioma macular degeneration major depressive disorder melancholic depression melanoma microphthalmia mixed glioma mongolian spot myocardial infarction myopathy myositis myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuropathy neurotic disorder nicotine dependence obesity obsolete Matthew-Wood syndrome obsolete congenital ichthyosiform erythroderma obsolete melancholia ocular melanoma osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma peripheral nervous system disease pleomorphic liposarcoma polycystic ovary syndrome prediabetes syndrome premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia proliferative diabetic retinopathy prostate cancer prostate carcinoma pseudoxanthoma elasticum psychologic dyspareunia rectal benign neoplasm rectum adenocarcinoma rectum cancer retinal disease retinitis pigmentosa retinitis retinoblastoma retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis schizophrenia sensorineural hearing loss silent myocardial infarction skin melanoma steatotic liver disease stomach cancer stomach carcinoma systemic primary carnitine deficiency disease trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
Q96AC1	Fermitin family homolog 2	FERMT2 KIND2 MIG2 PLEKHC1	Homo sapiens (human)	0	1
Q96A99	Pentraxin-4	PTX4 C16orf38	Homo sapiens (human)	2	0
Q96A84	EMI domain-containing protein 1	EMID1 EMU1	Homo sapiens (human)	2	0
Q96A83	Collagen alpha-1(XXVI) chain	COL26A1 EMID2 EMU2	Homo sapiens (human)	8	9
Q96A73	Putative monooxygenase p33MONOX	KIAA1191 P33MONOX	Homo sapiens (human)	2	1
Q96A72	Protein mago nashi homolog 2	MAGOHB MAGOH2	Homo sapiens (human)	0	1
Q96A65	Exocyst complex component 4	EXOC4 KIAA1699 SEC8 SEC8L1	Homo sapiens (human)	1	2
Q96A49	Synapse-associated protein 1	SYAP1	Homo sapiens (human)	4	2
Q96A44	SPRY domain-containing SOCS box protein 4	SPSB4 SSB4	Homo sapiens (human)	1	1
Q96A35	Large ribosomal subunit protein uL24m	MRPL24	Homo sapiens (human)	0	1
Q96A33	PAT complex subunit CCDC47	CCDC47	Homo sapiens (human)	3	3
Q96A28	SLAM family member 9	SLAMF9 CD2F10	Homo sapiens (human)	2	0
Q96A26	Protein FAM162A	FAM162A C3orf28 E2IG5	Homo sapiens (human)	0	1
Q96A23	Copine-4	CPNE4	Homo sapiens (human)	0	1
Q96A19	Coiled-coil domain-containing protein 102A	CCDC102A	Homo sapiens (human)	0	1
Q96A11	Galactose-3-O-sulfotransferase 3	GAL3ST3	Homo sapiens (human)	4	0
Q96A09	Terminal nucleotidyltransferase 5B	TENT5B FAM46B	Homo sapiens (human)	0	1
Q96A08	Histone H2B type 1-A	H2BC1 HIST1H2BA TSH2B	Homo sapiens (human)	0	1
Q96A00	Protein phosphatase 1 regulatory subunit 14A	PPP1R14A CPI17 PPP1INL	Homo sapiens (human)	0	1
Q969Z4	Tumor necrosis factor receptor superfamily member 19L	RELT TNFRSF19L	Homo sapiens (human)	1	0
Q969Z0	FAST kinase domain-containing protein 4	TBRG4 CPR2 FASTKD4 KIAA0948	Homo sapiens (human)	1	2

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