GlyCosmos Portal

Displaying entries **1701 - 1725** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P51654	Glypican-3	GPC3 OCI5	6	11	Beckwith-Wiedemann syndrome CLOVES syndrome Crouzon syndrome Dandy-Walker syndrome Laron syndrome Marfan syndrome Meckel syndrome Meckel's diverticulum Perlman syndrome Proteus syndrome Simpson-Golabi-Behmel syndrome type 1 Sotos syndrome achondroplasia adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adult endodermal sinus tumor adult hepatocellular carcinoma adult medulloblastoma alcoholic liver cirrhosis ameloblastoma aniridia arthritis arthropathy 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 atypical teratoid rhabdoid tumor autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant polycystic kidney disease basal cell carcinoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer childhood hepatocellular carcinoma childhood medulloblastoma cholangiocarcinoma chondrosarcoma chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma cleft lip cleft palate clubfoot collecting duct carcinoma colorectal cancer colorectal carcinoma communicating hydrocephalus congenital diaphragmatic hernia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital mesoblastic nephroma craniosynostosis cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic kidney disease dextro-looped transposition of the great arteries distal arthrogryposis double outlet right ventricle early infantile epileptic encephalopathy embryoma embryonal cancer endodermal sinus tumor endometrial cancer endometrial carcinoma endometrial clear cell adenocarcinoma endomyocardial fibrosis epilepsy epithelioid sarcoma essential hypertension familial nephrotic syndrome follicular adenoma gallbladder cancer gallbladder carcinoma gallbladder disease germ cell and embryonal cancer germ cell cancer germinoma granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hidradenoma hydrocephalus hydronephrosis hypertension hypertrophic cardiomyopathy hypoglycemia immune system disease inguinal hernia intellectual disability intrahepatic cholangiocarcinoma isolated cleft palate large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy lipoid nephrosis liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microcystic adenoma mucinous adenocarcinoma multiple types of congenital heart defects 6 nephroblastoma nephrotic syndrome type 1 nephrotic syndrome neuroblastoma neuroendocrine carcinoma nevoid basal cell carcinoma syndrome non-congenital cyst of kidney nonpapillary renal cell carcinoma nonsyndromic congenital nail disorder 9 obsolete Opitz-GBBB syndrome obsolete dextro-looped transposition of the great arteries 1 obsolete mesoblastic nephroma obstructive hydrocephalus omphalocele osteoarthritis ovarian cancer ovarian carcinoma ovarian embryonal carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma patent ductus arteriosus patent foramen ovale placental insufficiency polydactyly polyhydramnios primary immunodeficiency disease prostate cancer prostate carcinoma renal agenesis renal carcinoma renal cell carcinoma rhabdoid cancer rhabdomyosarcoma salivary gland adenoid cystic carcinoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scoliosis sebaceous carcinoma seminoma senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag speech disorder spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma sweat gland cancer syringoma testicular cancer testicular germ cell cancer thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma umbilical hernia uterine corpus cancer ventricular septal defect viral infectious disease visual epilepsy
O95502	Neuronal pentraxin receptor	NPTXR	6	5
Q14847	LIM and SH3 domain protein 1	LASP1 MLN50	6	2
Q9UK23	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA	6	2	Fabry disease alexia chylomicron retention disease dyslexia glycoproteinosis lipid storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis III mucopolysaccharidosis type IIIB neurodegenerative disease stuttering
Q6ZNA5	Ferric-chelate reductase 1	FRRS1 SDFR2 SDR2	6	8
P07738	Bisphosphoglycerate mutase	BPGM	6	0	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 normocytic anemia polycythemia vera polycythemia stress polycythemia
Q9H2U9	Disintegrin and metalloproteinase domain-containing protein 7	ADAM7 GP83	6	0
Q9HCL0	Protocadherin-18	PCDH18 KIAA1562	6	0
Q9HB40	Retinoid-inducible serine carboxypeptidase	SCPEP1 RISC SCP1	6	5
Q9Y5B9	FACT complex subunit SPT16	SUPT16H FACT140 FACTP140	6	2
O95838	Glucagon-like peptide 2 receptor	GLP2R	6	1
Q6MZM0	Ferroxidase HEPHL1	HEPHL1	6	0
A4D0V7	Cadherin-like and PC-esterase domain-containing protein 1	CPED1 C7orf58	6	0
P20309	Muscarinic acetylcholine receptor M3	CHRM3	6	1
Q8TDW0	Volume-regulated anion channel subunit LRRC8C	LRRC8C AD158 FAD158	6	5
P49755	Transmembrane emp24 domain-containing protein 10	TMED10 TMP21	6	3
Q14982	Opioid-binding protein/cell adhesion molecule	OPCML IGLON1 OBCAM	6	0	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma adenocarcinoma adenoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cholangiocarcinoma congenital heart disease cribriform carcinoma depressive disorder dermoid cyst of ovary distal arthrogryposis dysgerminoma embryoma esophagus squamous cell carcinoma gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma idiopathic scoliosis intrahepatic cholangiocarcinoma liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder melancholic depression mixed glioma nasopharynx carcinoma neurotic disorder nicotine dependence obsolete melancholia obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma prostate lymphoma sarcomatoid carcinoma schizophrenia steatotic liver disease stomach cancer stomach carcinoma tubular adenocarcinoma urinary bladder cancer
P06870	Kallikrein-1	KLK1	6	28
A0A0G2JL69	Complement C2	C2	6	0
Q92186	Alpha-2,8-sialyltransferase 8B	ST8SIA2 SIAT8B STX	6	0	adenocarcinoma adenoma allergic rhinitis anaplastic astrocytoma autism spectrum disorder autistic disorder bipolar disorder breast cancer breast carcinoma cancer childhood cerebral astrocytoma colitis cribriform carcinoma diarrhea disease of mental health embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma granular cell carcinoma hemolytic-uremic syndrome high grade glioma ileitis ileocolitis intestinal infectious disease juvenile pilocytic astrocytoma lung cancer lung non-small cell carcinoma malignant astrocytoma mood disorder neuroblastoma pilocytic astrocytoma protoplasmic astrocytoma psychotic disorder rhabdomyosarcoma schizophrenia shigellosis subependymal giant cell astrocytoma tubular adenocarcinoma vasomotor rhinitis
P0DN87	Choriogonadotropin subunit beta 7	CGB7	6	0
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
Q9H6E4	Coiled-coil domain-containing protein 134	CCDC134	6	2
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
P05543	Thyroxine-binding globulin	SERPINA7 TBG	6	41

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