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 **13251 - 13275** 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
Q9H8K7	ATPase PAAT	PAAT C10orf88	Homo sapiens (human)	0	1
Q96E09	PPP2R1A-PPP2R2A-interacting phosphatase regulator 1	PABIR1 C9orf42 FAM122A	Homo sapiens (human)	0	1
Q7Z309	PABIR family member 2	PABIR2 FAM122B	Homo sapiens (human)	4	2
P11940	Polyadenylate-binding protein 1	PABPC1 PAB1 PABP PABP1 PABPC2	Homo sapiens (human)	6	2
Q4VXU2	Polyadenylate-binding protein 1-like	PABPC1L C20orf119	Homo sapiens (human)	0	1
Q9H361	Polyadenylate-binding protein 3	PABPC3 PABP3 PABPL3	Homo sapiens (human)	3	2
Q13310	Polyadenylate-binding protein 4	PABPC4 APP1 PABP4	Homo sapiens (human)	2	1
Q86U42	Polyadenylate-binding protein 2	PABPN1 PAB2 PABP2	Homo sapiens (human)	8	1
Q9H813	Proton-activated chloride channel	PACC1 C1orf75 TMEM206	Homo sapiens (human)	3	3
Q8N7B6	PACRG-like protein	PACRGL C4orf28	Homo sapiens (human)	1	1
Q6VY07	Phosphofurin acidic cluster sorting protein 1	PACS1 KIAA1175	Homo sapiens (human)	3	1
Q86VP3	Phosphofurin acidic cluster sorting protein 2	PACS2 KIAA0602 PACS1L	Homo sapiens (human)	2	1
Q9UNF0	Protein kinase C and casein kinase substrate in neurons protein 2	PACSIN2	Homo sapiens (human)	1	1
Q9UKS6	Protein kinase C and casein kinase substrate in neurons protein 3	PACSIN3	Homo sapiens (human)	0	1
Q9ULC6	Protein-arginine deiminase type-1	PADI1 PAD1 PDI1	Homo sapiens (human)	1	1
Q9UM07	Protein-arginine deiminase type-4	PADI4 PAD4 PADI5 PDI5	Homo sapiens (human)	0	1
Q6TGC4	Protein-arginine deiminase type-6	PADI6 PAD6	Homo sapiens (human)	1	1
P09466	Glycodelin	PAEP	Homo sapiens (human)	3	42
Q8N7H5	RNA polymerase II-associated factor 1 homolog	PAF1 PD2	Homo sapiens (human)	3	1
P43034	Platelet-activating factor acetylhydrolase IB subunit beta	PAFAH1B1 LIS1 MDCR MDS PAFAHA	Homo sapiens (human)	0	1	3p deletion syndrome Alzheimer's disease Angelman syndrome B-cell lymphoma Behcet's disease Crohn's colitis Crohn's disease Ewing sarcoma Gaucher's disease type I Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Joubert syndrome Langerhans-cell histiocytosis Marfan syndrome Miller-Dieker lissencephaly syndrome NFIA-related disorder Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease REM sleep behavior disorder Rett syndrome SATB2-associated syndrome Shwachman-Diamond syndrome Smith-Magenis syndrome West syndrome X-linked juvenile retinoschisis 1 Zellweger syndrome acute monocytic leukemia acute myeloid leukemia adult medulloblastoma adult respiratory distress syndrome aggressive periodontitis allergic asthma alternating hemiplegia of childhood anxiety disorder aplastic anemia asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer central nervous system disease childhood acute myeloid leukemia childhood leukemia childhood medulloblastoma childhood osteosarcoma chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17p13.1 deletion syndrome chromosome 17p13.3 duplication syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic monocytic leukemia chronic myelomonocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome dementia depressive disorder distal 10q deletion syndrome distal arthrogryposis dysthymic disorder dystonia embryoma epilepsy essential thrombocythemia essential tremor familial adenomatous polyposis 1 familial adenomatous polyposis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis hematologic cancer hepatocellular carcinoma high grade glioma hydranencephaly hydrocephalus impulse control disorder inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia kidney disease kleptomania late onset Parkinson's disease learning disability leukemia lingual-facial-buccal dyskinesia lissencephaly liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephaly mood disorder movement disease multiple myeloma multiple system atrophy myelodysplastic syndrome myelodysplastic/myeloproliferative neoplasm myeloproliferative neoplasm nephritis nephrosis nervous system disease neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete constipation obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus oculocerebrorenal syndrome omphalocele osteosarcoma papillary renal cell carcinoma periodontosis periventricular nodular heterotopia peroxisome biogenesis disorder 1A phobic disorder polycystic ovary syndrome polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postural orthostatic tachycardia syndrome progressive supranuclear palsy psychotic disorder pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinitis pigmentosa 13 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder subcortical band heterotopia syndromic X-linked intellectual disability Najm type trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis ulcerative colitis umbilical hernia vascular disease visual epilepsy
P68402	Platelet-activating factor acetylhydrolase IB subunit alpha2	PAFAH1B2 PAFAHB	Homo sapiens (human)	0	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 cancer cerebral degeneration embryoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma
Q15102	Platelet-activating factor acetylhydrolase IB subunit alpha1	PAFAH1B3 PAFAHG	Homo sapiens (human)	0	1	intellectual disability learning disability
Q9BTK6	PAXIP1-associated glutamate-rich protein 1	PAGR1 C16orf53 PA1	Homo sapiens (human)	4	1
P22234	Bifunctional phosphoribosylaminoimidazole carboxylase/phosphoribosylaminoimidazole succinocarboxamide synthetase	PAICS ADE2 AIRC PAIS	Homo sapiens (human)	0	1
Q9H074	Polyadenylate-binding protein-interacting protein 1	PAIP1	Homo sapiens (human)	1	1

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