GlyCosmos Portal

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q12980	GATOR1 complex protein NPRL3	NPRL3 C16orf35 CGTHBA MARE	2	3
Q9NXC5	GATOR2 complex protein MIOS	MIOS	0	1
Q96S15	GATOR2 complex protein WDR24	WDR24 C16orf21	2	2
H8Y6P7	GCOM1, MYZAP-POLR2M combined locus	GCOM1	1	1
O95479	GDH/6PGL endoplasmic bifunctional protein	H6PD GDH	3	20	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
P56159	GDNF family receptor alpha-1	GFRA1 GDNFRA RETL1 TRNR1	6	14	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 B-cell lymphoma Hirschsprung's disease Kennedy's disease Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
O00451	GDNF family receptor alpha-2	GFRA2 GDNFRB RETL2 TRNR2	6	6	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
O60609	GDNF family receptor alpha-3	GFRA3	4	1
Q9GZZ7	GDNF family receptor alpha-4	GFRA4	1	0	Hirschsprung's disease allergic asthma asthma intrinsic asthma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A panic disorder
Q6UXV0	GDNF family receptor alpha-like	GFRAL C6orf144	6	0
Q9H116	GDNF-inducible zinc finger protein 1	GZF1 ZBTB23 ZNF336	0	1
Q13630	GDP-L-fucose synthase	GFUS SDR4E1 TSTA3	0	1
Q2TAA5	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	ALG11 GT8	2	1	cerebral degeneration congenital disorder of glycosylation Ip congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia inherited metabolic disorder intellectual disability learning disability mechanical strabismus microcephaly ophthalmoplegia scoliosis sensorineural hearing loss strabismus visual epilepsy
Q9H488	GDP-fucose protein O-fucosyltransferase 1	POFUT1 FUT12 KIAA0180	2	17	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
O60547	GDP-mannose 4,6 dehydratase	GMDS	0	1	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
Q9BUV8	GEL complex subunit OPTI	RAB5IF C20orf24 OPTI RCAF1	1	1
Q8N2G8	GH3 domain-containing protein	GHDC D11LGP1E LGP1	1	1
Q6UWM5	GLIPR1-like protein 1	GLIPR1L1	1	0
Q9P2T1	GMP reductase 2	GMPR2	0	1
P49915	GMP synthase [glutamine-hydrolyzing]	GMPS	3	6
Q3T8J9	GON-4-like protein	GON4L GON4 KIAA1606	1	1
Q8IXQ4	GPALPP motifs-containing protein 1	GPALPP1 KIAA1704 LSR7	4	2
O95427	GPI ethanolamine phosphate transferase 1	PIGN MCD4	4	8	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia 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 autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
Q5H8A4	GPI ethanolamine phosphate transferase 2	PIGG GPI7	1	0	cerebral degeneration epilepsy intellectual disability learning disability placental insufficiency visual epilepsy

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