GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q9Y2I8	WD repeat-containing protein 37	WDR37 KIAA0982	3	1
Q6ZTQ4	Cadherin-related family member 3	CDHR3 CDH28	3	0
B0FYL7	MICA protein (Fragment)	MICA	3	0
Q5VT25	Serine/threonine-protein kinase MRCK alpha	CDC42BPA KIAA0451	3	2
Q6ZVN8	Hemojuvelin	HJV HFE2 RGMC	3	1	Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kallmann syndrome Meckel syndrome 8 Sheehan syndrome Wilson disease X-linked dilated cardiomyopathy amenorrhea anaplastic astrocytoma androgen insensitivity syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autosomal recessive polycystic kidney disease azoospermia bacterial infectious disease beta thalassemia breast cancer breast carcinoma cardiomyopathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma cholestasis chronic kidney disease congenital hypothyroidism congenital nongoitrous hypothyroidism 4 congestive heart failure coronary artery disease diabetes mellitus diabetic ketoacidosis 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 endomyocardial fibrosis essential hypertension essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma hemochromatosis type 1 hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatitis C hepatocellular carcinoma high grade glioma hypertension hypertrophic cardiomyopathy hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism impotence infertility iron metabolism disease isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor liver cancer lung squamous cell carcinoma malignant astrocytoma marasmus microcytic anemia middle cerebral artery infarction muscular dystrophy myelodysplastic syndrome myxedema neurogenic arthropathy nutrition disease obesity osteoporosis panhypopituitarism pilocytic astrocytoma polycystic kidney disease 4 porphyria cutanea tarda premature ejaculation protein-energy malnutrition protoplasmic astrocytoma psychologic dyspareunia sick sinus syndrome steatotic liver disease subependymal giant cell astrocytoma thalassemia
Q15018	BRISC complex subunit Abraxas 2	ABRAXAS2 ABRO1 FAM175B KIAA0157	3	2
F5CJX6	Major histocompatibility complex class I chain-related protein A (Fragment)	MICA	3	0
P00739	Haptoglobin-related protein	HPR	3	0
P61073	C-X-C chemokine receptor type 4	CXCR4	3	0
O94763	Unconventional prefoldin RPB5 interactor 1	URI1 C19orf2 NNX3 PPP1R19 RMP URI	3	1
Q96FC7	Phytanoyl-CoA hydroxylase-interacting protein-like	PHYHIPL KIAA1796	3	1
Q9Y5I0	Protocadherin alpha-13	PCDHA13 CNRS5	3	0
P35504	UDP-glucuronosyltransferase 1A5	UGT1A5 GNT1 UGT1	3	2	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis diabetes mellitus embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D influenza leukopenia liver disease neonatal jaundice neutropenia obesity prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
Q6ZS10	C-type lectin domain family 17, member A	CLEC17A	3	0	Richter's syndrome chronic lymphocytic leukemia
Q9H582	Zinc finger protein 644	ZNF644 KIAA1221 ZEP2	3	1
D6REQ6	Ribonuclease T2	RNASET2	3	0
P17858	ATP-dependent 6-phosphofructokinase, liver type	PFKL	3	6	Down syndrome Lafora disease Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis bipolar disorder coronary artery disease cystinuria dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma liver cancer mood disorder obsolete major affective disorder 1 obsolete major affective disorder 2 progressive myoclonus epilepsy 1A progressive myoclonus epilepsy tetralogy of Fallot ventricular septal defect
Q9BY42	Replication termination factor 2	RTF2 C20orf43 RTFDC1	3	1
P14780	Matrix metalloproteinase-9	MMP9 CLG4B	3	40
Q8NH07	Olfactory receptor 11H2	OR11H2 C14orf15 OR11H2P	3	0
Q5VX71	Sushi domain-containing protein 4	SUSD4	3	0
A0AVL1	ADAM metallopeptidase domain 9	ADAM9	3	0
Q9NQS5	G-protein coupled receptor 84	GPR84 EX33	3	1
O96009	Napsin-A	NAPSA NAP1 NAPA	3	77
P33240	Cleavage stimulation factor subunit 2	CSTF2	3	1

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