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 **13626 - 13650** 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
Q6ZVD8	PH domain leucine-rich repeat-containing protein phosphatase 2	PHLPP2 KIAA0931 PHLPPL	Homo sapiens (human)	4	1
Q8TCT1	Phosphoethanolamine/phosphocholine phosphatase	PHOSPHO1	Homo sapiens (human)	0	1	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
Q9NRX4	14 kDa phosphohistidine phosphatase	PHPT1 PHP14	Homo sapiens (human)	0	1
Q9P1Y6	PHD and RING finger domain-containing protein 1	PHRF1 KIAA1542	Homo sapiens (human)	4	2
Q9UMS5	Protein PHTF1	PHTF1 PHTF	Homo sapiens (human)	9	2
Q8N3S3	Protein PHTF2	PHTF2	Homo sapiens (human)	3	0
Q5SRE7	Phytanoyl-CoA dioxygenase domain-containing protein 1	PHYHD1	Homo sapiens (human)	0	1
Q92561	Phytanoyl-CoA hydroxylase-interacting protein	PHYHIP DYRK1AP3 KIAA0273	Homo sapiens (human)	2	1
Q96FC7	Phytanoyl-CoA hydroxylase-interacting protein-like	PHYHIPL KIAA1796	Homo sapiens (human)	3	1
O43692	Peptidase inhibitor 15	PI15 CRISP8 P25TI	Homo sapiens (human)	3	1
Q6UXB8	Peptidase inhibitor 16	PI16 CRISP9 PSPBP	Homo sapiens (human)	21	6
Q9BTU6	Phosphatidylinositol 4-kinase type 2-alpha	PI4K2A	Homo sapiens (human)	0	1	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
P42356	Phosphatidylinositol 4-kinase alpha	PI4KA PIK4 PIK4CA	Homo sapiens (human)	4	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 CEDNIK syndrome Pick's disease Reye syndrome anemia cancer cerebral degeneration clubfoot disease of mental health hepatitis C hepatocellular carcinoma hypomyelinating leukodystrophy 2 liver cancer macrocytic anemia prostate cancer prostate carcinoma psychotic disorder schizophrenia
A4QPH2	Putative phosphatidylinositol 4-kinase alpha-like protein P2	PI4KAP2	Homo sapiens (human)	1	1
Q9UBF8	Phosphatidylinositol 4-kinase beta	PI4KB PIK4CB	Homo sapiens (human)	0	1	EAST syndrome hepatitis C severe acute respiratory syndrome
Q8IYJ0	PILR alpha-associated neural protein	PIANP C12orf53 PANP	Homo sapiens (human)	1	0
O75925	E3 SUMO-protein ligase PIAS1	PIAS1 DDXBP1	Homo sapiens (human)	1	2
O75928	E3 SUMO-protein ligase PIAS2	PIAS2 PIASX	Homo sapiens (human)	1	2
Q13492	Phosphatidylinositol-binding clathrin assembly protein	PICALM CALM	Homo sapiens (human)	29	3
Q7Z2X4	PTB-containing, cubilin and LRP1-interacting protein	PID1 NYGGF4 PCLI1	Homo sapiens (human)	0	1
Q9HB75	p53-induced death domain-containing protein 1	PIDD1 LRDD PIDD	Homo sapiens (human)	1	1
Q92508	Piezo-type mechanosensitive ion channel component 1	PIEZO1 FAM38A KIAA0233	Homo sapiens (human)	3	10
Q9H5I5	Piezo-type mechanosensitive ion channel component 2	PIEZO2 C18orf30 C18orf58 FAM38B	Homo sapiens (human)	7	4
P37287	Phosphatidylinositol N-acetylglucosaminyltransferase subunit A	PIGA	Homo sapiens (human)	1	0	Barrett's esophagus Burkitt lymphoma Hirschsprung's disease Marfan syndrome Miller-Dieker lissencephaly syndrome Simpson-Golabi-Behmel syndrome type 1 Simpson-Golabi-Behmel syndrome type 2 Unverricht-Lundborg syndrome West syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency aplastic anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atypical hemolytic-uremic syndrome autoimmune disease autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B blepharospasm blood coagulation disease bone marrow cancer brain disease cancer chondroma chromosome 17p13.1 deletion syndrome coronary thrombosis dental caries dentin caries developmental and epileptic encephalopathy 3 early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy esophagitis esophagus adenocarcinoma essential thrombocythemia extramedullary plasmacytoma fetal erythroblastosis focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth hematopoietic system disease hemoglobinuria hemolytic anemia hemolytic-uremic syndrome immune system disease inflammatory bowel disease intellectual disability learning disability lissencephaly multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction obsolete congenital ichthyosiform erythroderma obsolete infantile epileptic encephalopathy paroxysmal nocturnal hemoglobinuria patent foramen ovale peptic esophagitis plasma cell neoplasm plasmacytoma polycythemia vera primary pulmonary hypertension protein C deficiency protein S deficiency pulmonary embolism sensorineural hearing loss silent myocardial infarction situs inversus thrombophilia thrombotic thrombocytopenic purpura transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis vertebrobasilar insufficiency visual epilepsy
Q92521	GPI mannosyltransferase 3	PIGB	Homo sapiens (human)	2	0	axonal neuropathy epilepsy intellectual disability learning disability visual epilepsy

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