GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P05187	Alkaline phosphatase, placental type	ALPP PLAP	2	1	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 Becker muscular dystrophy Bloom syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Marfan syndrome Pick's disease Q fever Reye syndrome Sjogren's syndrome Waardenburg syndrome type 1 Waardenburg syndrome Wilson disease X-linked lymphoproliferative syndrome 2 absence epilepsy achondroplasia acromegaly acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult cystic teratoma adult hypophosphatasia adult lymphoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis ankylosing spondylitis autoimmune pancreatitis 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 azoospermia bladder carcinoma bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease cartilage disease central nervous system lymphoma cerebral degeneration cerebral palsy cervical adenocarcinoma cervical cancer cervix carcinoma childhood absence epilepsy childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation connective tissue disease craniosynostosis cystic teratoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis distal myopathy dysplastic nevus syndrome embryoma embryonal cancer endemic goiter endometriosis of uterus endometriosis endomyocardial fibrosis esophagitis essential thrombocythemia exanthem extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypocalciuric hypercalcemia 1 fragile X syndrome gallbladder disease gastroesophageal reflux disease gastrointestinal system cancer germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glaucoma glioblastoma goiter heart disease hematologic cancer hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypercalcemia hyperpituitarism hypogonadism hypophosphatasia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis infantile hypophosphatasia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intrahepatic cholangiocarcinoma iron metabolism disease islet cell tumor isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer leukemia limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma malignant pleural mesothelioma malignant teratoma mature teratoma melanoma multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nasopharynx carcinoma nephrocalcinosis nephrolithiasis neuroblastoma neurodegenerative disease non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter 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 obsolete constipation obsolete ymphosarcoma obstructive lung disease oculopharyngeal muscular dystrophy osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis periodontitis phosphorus metabolism disease placenta cancer pleomorphic lipoma primary biliary cholangitis primary hyperparathyroidism progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma rhabdomyosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy steatotic liver disease stomach cancer stomach carcinoma subcortical band heterotopia substernal goiter teratoma testicular cancer testicular germ cell cancer testis seminoma thyroid gland disease trypanosomiasis tuberculosis tuberous sclerosis type 2 diabetes mellitus typhus ulcerative colitis uremia uric acid nephrolithiasis urinary bladder cancer uveal melanoma vitelliform macular dystrophy well-differentiated liposarcoma
Q8N1G4	Leucine-rich repeat-containing protein 47	LRRC47 KIAA1185	2	1
P58417	Neurexophilin-1	NXPH1 NPH1	6	1
Q15466	Nuclear receptor subfamily 0 group B member 2	NR0B2 SHP	0	1
Q9UMQ6	Calpain-11	CAPN11	0	1
A6NMX2	Eukaryotic translation initiation factor 4E type 1B	EIF4E1B	0	1
Q6J272	Ciliary microtubule inner protein 2A	CIMIP2A FAM166A	0	1
O14647	Chromodomain-helicase-DNA-binding protein 2	CHD2	2	1
Q9UL54	Serine/threonine-protein kinase TAO2	TAOK2 KIAA0881 MAP3K17 PSK PSK1	1	1
Q5TF21	Microtubule cross-linking factor 3	MTCL3 C6orf174 SOGA3	2	1
P51580	Thiopurine S-methyltransferase	TPMT	0	1
Q9UBE0	SUMO-activating enzyme subunit 1	SAE1 AOS1 SUA1 UBLE1A	0	1
Q9HAU5	Regulator of nonsense transcripts 2	UPF2 KIAA1408 RENT2	1	1
Q8WXX0	Dynein axonemal heavy chain 7	DNAH7 KIAA0944	1	1
Q5C9Z4	Nucleolar MIF4G domain-containing protein 1	NOM1 C7orf3	1	1
Q9HB20	Pleckstrin homology domain-containing family A member 3	PLEKHA3 FAPP1	0	1
Q6PIV2	Forkhead box protein R1	FOXR1 FOXN5	0	1
Q96LW4	DNA-directed primase/polymerase protein	PRIMPOL CCDC111	1	1
Q00888	Pregnancy-specific beta-1-glycoprotein 4	PSG4 CGM4 PSG9	6	1
Q494V2	Cilia- and flagella-associated protein 100	CFAP100 CCDC37	1	1
E5RQL4	Formiminotransferase N-terminal subdomain-containing protein	FTCDNL1 FONG	0	1
O94811	Tubulin polymerization-promoting protein	TPPP TPPP1	4	1
Q6NVY1	3-hydroxyisobutyryl-CoA hydrolase, mitochondrial	HIBCH	0	1	Leigh disease Unverricht-Lundborg syndrome West syndrome agnosia arthritis arthropathy blepharospasm brain disease cancer colorectal cancer colorectal carcinoma congenital nystagmus cryptorchidism developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy epilepsy focal hand dystonia generalized dystonia hydrocephalus hypertropia inherited metabolic disorder lactic acidosis large intestine cancer mechanical strabismus neurodegenerative disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus spontaneous ocular nystagmus strabismus tetralogy of Fallot visual epilepsy
Q14135	Transcription cofactor vestigial-like protein 4	VGLL4 KIAA0121	0	1
Q6ZN03	Putative uncharacterized protein encoded by LINC00322	LINC00322 C21orf136 NCRNA00322	1	1

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