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 **15976 - 16000** 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
P25024	C-X-C chemokine receptor type 1	CXCR1 CMKAR1 IL8RA	Homo sapiens (human)	4	1
Q9UHF7	Zinc finger transcription factor Trps1	TRPS1	Homo sapiens (human)	4	1
Q99795	Cell surface A33 antigen	GPA33	Homo sapiens (human)	4	1
Q9NY72	Sodium channel regulatory subunit beta-3	SCN3B KIAA1158	Homo sapiens (human)	4	0
P43116	Prostaglandin E2 receptor EP2 subtype	PTGER2	Homo sapiens (human)	4	0
Q9ULD8	Potassium voltage-gated channel subfamily H member 3	KCNH3 KIAA1282	Homo sapiens (human)	4	1
J3QR68	Haptoglobin (Fragment)	HP	Homo sapiens (human)	4	0
O00476	Sodium-dependent phosphate transport protein 4	SLC17A3 NPT4	Homo sapiens (human)	4	0
P51178	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1	PLCD1	Homo sapiens (human)	4	1	Marfan syndrome actinic keratosis alopecia amyotrophic lateral sclerosis arthritis arthropathy blepharitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic myeloid leukemia colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary artery vasospasm cystic fibrosis diabetes mellitus embryoma esophagus squamous cell carcinoma essential hypertension glycoproteinosis hypertension impulse control disorder intermittent explosive disorder irritant dermatitis kleptomania large intestine cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mucolipidosis II alpha/beta nephrolithiasis nonsyndromic congenital nail disorder 3 obsolete Matthew-Wood syndrome obsolete asthenopia osteoarthritis parapsoriasis progressive muscular atrophy psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis situs inversus skin disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis
Q9BZM2	Group IIF secretory phospholipase A2	PLA2G2F	Homo sapiens (human)	4	0
P25101	Endothelin-1 receptor	EDNRA ETA ETRA	Homo sapiens (human)	4	3
Q9HAW7	UDP-glucuronosyltransferase 1A7	UGT1A7 GNT1 UGT1	Homo sapiens (human)	4	3	Crigler-Najjar syndrome Crohn's colitis Crohn's disease Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 acute pancreatitis adult hepatocellular carcinoma agranulocytosis alcoholic pancreatitis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest childhood hepatocellular carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma hemoglobin H disease hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis inflammatory bowel disease 1 inflammatory bowel disease influenza kernicterus due to isoimmunization kernicterus large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer leukopenia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma tracheal disease type 2 diabetes mellitus ulcerative colitis urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
Q7Z7C8	Transcription initiation factor TFIID subunit 8	TAF8 TAFII43 TBN	Homo sapiens (human)	4	1
Q9UP95	Solute carrier family 12 member 4	SLC12A4 KCC1	Homo sapiens (human)	5	7
Q7Z2Q7	Leucine-rich repeat-containing protein 70	LRRC70	Homo sapiens (human)	5	1
Q9BTN0	Leucine-rich repeat and fibronectin type-III domain-containing protein 3	LRFN3 SALM4	Homo sapiens (human)	5	1
P02745	Complement C1q subcomponent subunit A	C1QA	Homo sapiens (human)	5	47
Q9H3R1	Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 4	NDST4 HSST4	Homo sapiens (human)	5	1	arteriosclerotic cardiovascular disease atherosclerosis cancer colorectal cancer colorectal carcinoma coronary artery disease embryoma large intestine cancer nutmeg liver prostate cancer prostate carcinoma
P06126	T-cell surface glycoprotein CD1a	CD1A	Homo sapiens (human)	5	0
P49746	Thrombospondin-3	THBS3 TSP3	Homo sapiens (human)	5	38
Q2M2H8	Probable maltase-glucoamylase 2	MGAM2	Homo sapiens (human)	5	1
Q8NC54	Keratinocyte-associated transmembrane protein 2	KCT2 C5orf15	Homo sapiens (human)	5	2
P17050	Alpha-N-acetylgalactosaminidase	NAGA	Homo sapiens (human)	5	95	Clouston syndrome Fabry disease Kanzaki disease Schindler disease type 1 Unverricht-Lundborg syndrome acquired hyperkeratosis alternating hemiplegia of childhood autistic disorder autonomic neuropathy blepharospasm cancer cardiomyopathy cataract central nervous system disease central nervous system origin vertigo cerebral degeneration chylomicron retention disease congenital nystagmus dissociated nystagmus early myoclonic encephalopathy elephantiasis embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia gallbladder disease hypertrophic cardiomyopathy hypertropia influenza intellectual disability learning disability lipid storage disease liver disease lymphedema mechanical strabismus nervous system disease neuroaxonal dystrophy neurodegeneration with brain iron accumulation 2a neuropathy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 trichomoniasis visual epilepsy
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q07912	Activated CDC42 kinase 1	TNK2 ACK1	Homo sapiens (human)	5	1

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