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 **626 - 650** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
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
Q5KSL6	Diacylglycerol kinase kappa	DGKK	Homo sapiens (human)	1	1	Marfan syndrome agnosia arteriosclerotic cardiovascular disease atherosclerosis conduct disorder coronary artery disease developmental coordination disorder disease of mental health fragile X syndrome hepatocellular carcinoma hypospadias liver cancer prostate cancer prostate carcinoma situs inversus syndromic X-linked intellectual disability 94 tuberous sclerosis
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	Homo sapiens (human)	2	1	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
Q969N2	GPI transamidase component PIG-T	PIGT	Homo sapiens (human)	5	16	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	Homo sapiens (human)	0	1	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
Q8IWU6	Extracellular sulfatase Sulf-1	SULF1 KIAA1077	Homo sapiens (human)	10	44	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
P18085	ADP-ribosylation factor 4	ARF4 ARF2	Homo sapiens (human)	3	1	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease breast cancer cystic kidney disease giant cell glioblastoma glioblastoma hepatitis C high grade glioma ovarian cancer ovarian carcinoma
Q14697	Neutral alpha-glucosidase AB	GANAB G2AN KIAA0088	Homo sapiens (human)	3	6	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic liver disease
Q7Z443	Polycystin-1-like protein 3	PKD1L3	Homo sapiens (human)	7	1	Meckel syndrome autosomal dominant polycystic kidney disease cerebral infarction cerebrovascular disease episodic kinesigenic dyskinesia 1 prostate cancer prostate carcinoma
Q7Z442	Polycystin-1-like protein 2	PKD1L2 KIAA1879 PC1L2	Homo sapiens (human)	10	1	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
Q92485	Acid sphingomyelinase-like phosphodiesterase 3b	SMPDL3B ASML3B ASMLPD	Homo sapiens (human)	3	0	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
Q96B86	Repulsive guidance molecule A	RGMA RGM	Homo sapiens (human)	4	3	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
Q8NFI3	Cytosolic endo-beta-N-acetylglucosaminidase	ENGASE	Homo sapiens (human)	1	1	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
O15118	NPC intracellular cholesterol transporter 1	NPC1	Homo sapiens (human)	26	32	Niemann-Pick disease type C1
P61916	NPC intracellular cholesterol transporter 2	NPC2 HE1	Homo sapiens (human)	3	32	Niemann-Pick disease type C2
Q92484	Cyclic GMP-AMP phosphodiesterase SMPDL3A	SMPDL3A ASML3A	Homo sapiens (human)	7	20	Niemann-Pick disease endometriosis of ovary endometriosis of uterus endometriosis sphingolipidosis urinary bladder cancer
P37837	Transaldolase	TALDO1 TAL TALDO TALDOR	Homo sapiens (human)	0	1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma 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 autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
P08319	All-trans-retinol dehydrogenase [NAD(+)] ADH4	ADH4 ADH2	Homo sapiens (human)	1	5	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myeloid leukemia acute pancreatitis adenocarcinoma adenoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma cancer carcinoma childhood cerebral astrocytoma cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma flat ductal epithelial atypia gemistocytic astrocytoma granular cell carcinoma hepatitis C hepatocellular carcinoma high grade glioma invasive ductal carcinoma juvenile pilocytic astrocytoma liver cancer liver cirrhosis malignant astrocytoma migraine ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pharynx cancer pilocytic astrocytoma protoplasmic astrocytoma squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma
Q9H2K2	Poly [ADP-ribose] polymerase tankyrase-2	TNKS2 PARP5B TANK2 TNKL	Homo sapiens (human)	0	1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma cleft lip cribriform carcinoma depressive disorder diabetes mellitus endometrial cancer endometrial carcinoma granular cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia osteosarcoma skin benign neoplasm skin cancer squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer
Q9Y2H2	Phosphatidylinositide phosphatase SAC2	INPP5F KIAA0966 SAC2	Homo sapiens (human)	2	2	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease breast cancer diabetes mellitus diabetic ketoacidosis familial hyperlipidemia hyperglycemia type 2 diabetes mellitus
O95210	Starch-binding domain-containing protein 1	STBD1	Homo sapiens (human)	2	1	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease glycogen storage disease II
Q16842	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2	ST3GAL2 SIAT4B	Homo sapiens (human)	3	3	Parkinson's disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma late onset Parkinson's disease mucopolysaccharidosis IV mucopolysaccharidosis IVA nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
Q9Y5Z6	Beta-1,3-galactosyltransferase 1	B3GALT1	Homo sapiens (human)	2	0	Peters plus syndrome adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	Homo sapiens (human)	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
Q13454	Tumor suppressor candidate 3	TUSC3 N33	Homo sapiens (human)	2	2	Peutz-Jeghers syndrome agnosia autosomal recessive intellectual developmental disorder 7 autosomal recessive intellectual developmental disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration childhood osteosarcoma chondrosarcoma choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression microcephaly mixed glioma neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma partial motor epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tongue squamous cell carcinoma ulcerative colitis visual epilepsy von Hippel-Lindau disease

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