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 **5026 - 5050** 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
Q9H2J4	Phosducin-like protein 3	PDCL3 PhLP2A VIAF1	Homo sapiens (human)	0	1
Q13371	Phosducin-like protein	PDCL PHLOP1 PhLP1	Homo sapiens (human)	0	1
Q8WUM4	Programmed cell death 6-interacting protein	PDCD6IP AIP1 ALIX KIAA1375	Homo sapiens (human)	10	2
O75340	Programmed cell death protein 6	PDCD6 ALG2	Homo sapiens (human)	0	1
O14737	Programmed cell death protein 5	PDCD5 TFAR19	Homo sapiens (human)	0	1
Q53EL6	Programmed cell death protein 4	PDCD4 H731	Homo sapiens (human)	0	1
Q9BRP1	Programmed cell death protein 2-like	PDCD2L	Homo sapiens (human)	0	1
Q9BQ51	Programmed cell death 1 ligand 2	PDCD1LG2 B7DC CD273 PDCD1L2 PDL2	Homo sapiens (human)	5	0
Q14690	Protein RRP5 homolog	PDCD11 KIAA0185	Homo sapiens (human)	1	1
Q15116	Programmed cell death protein 1	PDCD1 PD1	Homo sapiens (human)	4	0
P20941	Phosducin	PDC	Homo sapiens (human)	0	1
Q13442	28 kDa heat- and acid-stable phosphoprotein	PDAP1 HASPP28	Homo sapiens (human)	0	1
P49585	Choline-phosphate cytidylyltransferase A	PCYT1A CTPCT PCYT1	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 Cockayne syndrome Down syndrome Graves' disease Laron syndrome Leber congenital amaurosis Pick's disease Prinzmetal angina Reye syndrome Richter's syndrome Turner syndrome X-linked dilated cardiomyopathy abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acquired color blindness acute chest syndrome acute myeloid leukemia acute myocardial infarction acute vascular insufficiency of intestine adult medulloblastoma alopecia anxiety disorder aortic aneurysm aortitis appendicitis arteriosclerotic cardiovascular disease arteriovenous malformation arteriovenous malformations of the brain astigmatism atherosclerosis atrial fibrillation 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 atrioventricular septal defect atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune thyroiditis blindness blue color blindness bone disease bone marrow cancer bone osteosarcoma brain cancer brain stem infarction bronchus cancer bronchus carcinoma cancer cardiac tamponade carotid artery thrombosis carotid stenosis cartilage disease cataract central sleep apnea cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia collagen disease colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness connective tissue disease corneal disease coronary artery anomaly coronary artery disease coronary stenosis coronary thrombosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma 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 dissociated nystagmus embryoma embryonal cancer endocarditis epilepsy episodic kinesigenic dyskinesia 1 esophageal cancer esophageal carcinoma essential hypertension extramedullary plasmacytoma familial adenomatous polyposis fibromyalgia fundus dystrophy generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gonadal dysgenesis head and neck cancer hematologic cancer hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hyperthyroidism impotence infective endocarditis insulinoma intellectual disability intermittent claudication intracranial aneurysm intracranial thrombosis intrahepatic cholangiocarcinoma intussusception islet cell tumor keratoconus large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma multiple myeloma myeloid leukemia myelomeningocele myeloproliferative neoplasm myocardial infarction myopia neuroendocrine carcinoma neuroendocrine tumor night blindness nutmeg liver obsolete asthenopia osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma patent foramen ovale pathologic nystagmus peripheral artery disease peripheral vascular disease phobic disorder plasmacytoma polycythemia vera premature ejaculation primary pulmonary hypertension prostate cancer prostate carcinoma psychologic dyspareunia pterygium pulmonary embolism red color blindness red-green color blindness rheumatoid arthritis schizophrenia scoliosis seminoma sensorineural hearing loss sick sinus syndrome silent myocardial infarction skin melanoma spina bifida spinocerebellar ataxia type 8 split hand-foot malformation 1 spondyloepimetaphyseal dysplasia, Strudwick type spontaneous ocular nystagmus squamous cell carcinoma squamous cell neoplasm subacute bacterial endocarditis superior mesenteric artery syndrome testicular cancer testis seminoma tethered spinal cord syndrome thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy
Q8NBM8	Prenylcysteine oxidase-like	PCYOX1L	Homo sapiens (human)	1	0
B7Z3Y2	Prenylcysteine oxidase 1	PCYOX1	Homo sapiens (human)	1	0
Q584P1	Prenylcysteine oxidase 1 (Fragment)	PCYOX1	Homo sapiens (human)	1	0
Q9UHG3	Prenylcysteine oxidase 1	PCYOX1 KIAA0908 PCL1	Homo sapiens (human)	4	67
A0A669KBG0	Proprotein convertase subtilisin/kexin type 9	PCSK9	Homo sapiens (human)	1	0
A0A669KB81	Proprotein convertase subtilisin/kexin type 9	PCSK9	Homo sapiens (human)	1	0
Q8NBP7	Proprotein convertase subtilisin/kexin type 9	PCSK9 NARC1	Homo sapiens (human)	1	1
Q16549	Proprotein convertase subtilisin/kexin type 7	PCSK7 LPC PC7 PC8 SPC7	Homo sapiens (human)	4	2
P29122	Proprotein convertase subtilisin/kexin type 6	PCSK6 PACE4	Homo sapiens (human)	4	2
A0A669KA35	Proprotein convertase subtilisin/kexin type 5	PCSK5	Homo sapiens (human)	1	0
Q5JSG7	Proprotein convertase subtilisin/kexin type 5 (Fragment)	PCSK5	Homo sapiens (human)	1	0
Q92824	Proprotein convertase subtilisin/kexin type 5	PCSK5 PC5 PC6	Homo sapiens (human)	12	0

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