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 **776 - 800** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9HA77	Probable cysteine--tRNA ligase, mitochondrial	CARS2	Homo sapiens (human)	1
Q9BYT8	Neurolysin, mitochondrial	NLN AGTBP KIAA1226	Homo sapiens (human)	1
Q6PGQ1	Aspartate-rich protein 1	DRICH1 C22orf43	Homo sapiens (human)	1
Q8IZE3	Protein-associating with the carboxyl-terminal domain of ezrin	SCYL3 PACE1	Homo sapiens (human)	1
Q9NVC6	Mediator of RNA polymerase II transcription subunit 17	MED17 ARC77 CRSP6 DRIP77 DRIP80 TRAP80	Homo sapiens (human)	1
Q93074	Mediator of RNA polymerase II transcription subunit 12	MED12 ARC240 CAGH45 HOPA KIAA0192 TNRC11 TRAP230	Homo sapiens (human)	1
Q8N393	Zinc finger protein 786	ZNF786	Homo sapiens (human)	1
Q6NYC1	Bifunctional arginine demethylase and lysyl-hydroxylase JMJD6	JMJD6 KIAA0585 PSR PTDSR	Homo sapiens (human)	1
P60903	Protein S100-A10	S100A10 ANX2LG CAL1L CLP11	Homo sapiens (human)	1
Q9UJ78	Zinc finger MYM-type protein 5	ZMYM5 ZNF198L1 ZNF237	Homo sapiens (human)	1
O75223	Gamma-glutamylcyclotransferase	GGCT C7orf24 CRF21	Homo sapiens (human)	1
Q9NUP9	Protein lin-7 homolog C	LIN7C MALS3 VELI3	Homo sapiens (human)	1
O95678	Keratin, type II cytoskeletal 75	KRT75 K6HF KB18	Homo sapiens (human)	1
Q5JX69	Protein FAM209B	FAM209B C20orf107	Homo sapiens (human)	1
Q5VT79	Annexin A8-like protein 1	ANXA8L1 ANXA8L2	Homo sapiens (human)	1
P61619	Protein transport protein Sec61 subunit alpha isoform 1	SEC61A1 SEC61A	Homo sapiens (human)	1
Q8IZ16	Sperm acrosome developmental regulator	SPACDR C7orf61	Homo sapiens (human)	1
P20073	Annexin A7	ANXA7 ANX7 SNX	Homo sapiens (human)	1	Fanconi anemia complementation group A Fanconi anemia Richter's syndrome acute myocardial infarction adenocarcinoma adenoma breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer childhood leukemia chronic lymphocytic leukemia colorectal cancer colorectal carcinoma coronary thrombosis craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma large intestine cancer leukemia liver cancer liver carcinoma malaria melanoma mixed glioma myocardial infarction nasopharynx carcinoma nodular prostate prostate cancer prostate carcinoma prostatic adenoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma tubular adenocarcinoma
P49585	Choline-phosphate cytidylyltransferase A	PCYT1A CTPCT PCYT1	Homo sapiens (human)	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
Q9UMY4	Sorting nexin-12	SNX12	Homo sapiens (human)	1
Q9NUU7	ATP-dependent RNA helicase DDX19A	DDX19A DDX19L	Homo sapiens (human)	1
Q9Y4E8	Ubiquitin carboxyl-terminal hydrolase 15	USP15 KIAA0529	Homo sapiens (human)	1
Q96E09	PPP2R1A-PPP2R2A-interacting phosphatase regulator 1	PABIR1 C9orf42 FAM122A	Homo sapiens (human)	1
Q96EN8	Molybdenum cofactor sulfurase	MOCOS	Homo sapiens (human)	1
P17021	Zinc finger protein 17	ZNF17 KIAA1947 KOX10	Homo sapiens (human)	1

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