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 **19576 - 19600** 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
F9URQ9	Serine-rich adhesin for platelets	lp_2793	Lactiplantibacillus plantarum WCFS1	0	1
A0A0A6YY72	Inosine monophosphate dehydrogenase 2 (Fragment)	Impdh2	Mus musculus (house mouse)	0	1
Q9NS86	LanC-like protein 2	LANCL2 GPR69B TASP	Homo sapiens (human)	0	1
D1LWU5	Kinetoplast DNA-associated protein 3	KAP3	Trypanosoma cruzi	0	1
P14778	Interleukin-1 receptor type 1	IL1R1 IL1R IL1RA IL1RT1	Homo sapiens (human)	6	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 Balkan nephropathy Behcet's disease Bloch-Sulzberger syndrome Crohn's colitis Crohn's disease Evans' syndrome Gilles de la Tourette syndrome Hantavirus hemorrhagic fever with renal syndrome Kawasaki disease Loeffler syndrome Paget's disease of bone Pick's disease Reye syndrome Wilson disease abdominal aortic aneurysm acrodermatitis actinic keratosis acute myeloid leukemia acute pericementitis adult lymphoma adult malignant schwannoma adult respiratory distress syndrome aggressive periodontitis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic disease ankylosing spondylitis arthritis arthropathy articular cartilage disease ascending cholangitis asthma atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura benign ependymoma bipolar disorder bone disease bone osteosarcoma breast cancer breast carcinoma cancer cardiovascular system disease cartilage disease cellular ependymoma central nervous system lymphoma cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood lymphoma childhood malignant schwannoma childhood osteosarcoma cholangitis chondromalacia choriocarcinoma chronic fatigue syndrome colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer complex regional pain syndrome connective tissue benign neoplasm connective tissue disease coronary artery disease cyclic hematopoiesis dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of ovary endometriosis of uterus endometriosis eosinophilic pneumonia epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor esophagitis essential hypertension familial nephrotic syndrome focal segmental glomerulosclerosis gastroenteritis gastroesophageal reflux disease gestational diabetes glomerulonephritis glucose intolerance gout heart disease heart valve disease hemochromatosis hepatitis C hepatitis high grade glioma hyperglycemia hypertension hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory myofibroblastic tumor intrinsic asthma iron metabolism disease juvenile myelomonocytic leukemia kidney disease large intestine cancer leiomyosarcoma lepromatous leprosy leukemia lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 major depressive disorder malaria malignant fibrous histiocytoma malignant peripheral nerve sheath tumor melancholic depression myelitis myxoid leiomyosarcoma myxopapillary ependymoma nephritis nephrosis nephrotic syndrome neurilemmoma neurofibrosarcoma neurogenic arthropathy neurotic disorder newborn respiratory distress syndrome obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma panic disorder papillary adenocarcinoma papillary ependymoma papillary renal cell carcinoma parapsoriasis peptic esophagitis periodontitis periodontosis placenta cancer pneumonia polycystic ovary syndrome prediabetes syndrome primary sclerosing cholangitis psoriasis pterygium pulmonary eosinophilia pulmonary tuberculosis pulpitis pustulosis of palm and sole pyoureter rhabdomyosarcoma rheumatoid arthritis schizophrenia scleroderma sclerosing cholangitis seborrheic keratosis skin disease suppurative cholangitis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis
Q86X59	Putative uncharacterized protein LINC02875	LINC02875 C17orf82	Homo sapiens (human)	0	1
O60763	General vesicular transport factor p115	USO1 VDP	Homo sapiens (human)	0	1
Q9C073	Protein FAM117A	FAM117A	Homo sapiens (human)	0	1
Q9WV25	Poly(U)-binding-splicing factor PUF60	Puf60 Siahbp1	Rattus norvegicus (Norway rat)	0	1
Q6ZTZ1	Myb/SANT-like DNA-binding domain-containing protein 1	MSANTD1 C4orf44	Homo sapiens (human)	0	1
Q96FX7	tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A	TRMT61A C14orf172 TRM61	Homo sapiens (human)	0	1
Q60634	Flotillin-2	Flot2 Esa1 M17s1	Mus musculus (house mouse)	0	1
Q9GZR7	ATP-dependent RNA helicase DDX24	DDX24	Homo sapiens (human)	2	1
Q9NZK7	Group IIE secretory phospholipase A2	PLA2G2E	Homo sapiens (human)	1	1	atopic dermatitis benign mastocytoma dermatitis extracutaneous mastocytoma indolent systemic mastocytosis mast cell neoplasm mastocytosis obesity
Q15633	RISC-loading complex subunit TARBP2	TARBP2 TRBP	Homo sapiens (human)	0	1
V5DQM2	Aldehyde dehydrogenase	TCDM_01424	Trypanosoma cruzi Dm28c	0	1
P41235	Hepatocyte nuclear factor 4-alpha	HNF4A HNF4 NR2A1 TCF14	Homo sapiens (human)	0	1
Q9UQE7	Structural maintenance of chromosomes protein 3	SMC3 BAM BMH CSPG6 SMC3L1	Homo sapiens (human)	2	1	Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 3 Cornelia de Lange syndrome Dubowitz syndrome Laron syndrome Marfan syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Peters anomaly Prader-Willi syndrome Roberts syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma allergic asthma anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis 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 attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome blepharitis blind hypotensive eye bone cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 32 multiple types cataract central nervous system lymphoma childhood lymphoma choanal atresia chondrodysplasia-pseudohermaphroditism syndrome chronic interstitial cystitis chronic monocytic leukemia cleft palate cleidocranial dysplasia clubfoot colon carcinoma colorectal cancer cone-rod dystrophy congenital diaphragmatic hernia congenital nystagmus congenital ptosis cornea plana coronary artery disease craniosynostosis cribriform carcinoma cryptorchidism dissociated nystagmus embryoma epilepsy esophagitis fundus albipunctatus gastroesophageal reflux disease generalized anxiety disorder gingivitis glaucoma gonadal dysgenesis granular cell carcinoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hypertrichosis hypertropia hypospadias inguinal hernia intellectual disability interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal volvulus intrinsic asthma isolated cleft palate kidney failure kwashiorkor large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia lymphoma marasmus mechanical strabismus megacolon microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly myeloid leukemia myopia neuropathy nutrition disease obsolete SC phocomelia syndrome obsolete ymphosarcoma ophthalmoplegia osteosarcoma patent foramen ovale pathologic nystagmus peptic esophagitis periodontitis peripheral nervous system disease placental insufficiency pneumonia prostate cancer prostate carcinoma protein-energy malnutrition prune belly syndrome ptosis pulmonary valve stenosis pyloric stenosis radioulnar synostosis retinitis pigmentosa sarcomatoid carcinoma sensorineural hearing loss situs inversus speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 thromboangiitis obliterans toxic megacolon trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma ventricular septal defect vesicoureteral reflux visual epilepsy
Q8WVH0	Complexin-3	CPLX3	Homo sapiens (human)	0	1
E9PZ00	Prosaposin	Psap	Mus musculus (house mouse)	4	1
P35321	Cornifin-A	SPRR1A	Homo sapiens (human)	0	1
Q9NRX2	Large ribosomal subunit protein bL17m	MRPL17 LIP2	Homo sapiens (human)	0	1
P21917	D(4) dopamine receptor	DRD4	Homo sapiens (human)	4	1
A0A1B0GUW6	Uncharacterized protein SPEM3	SPEM3	Homo sapiens (human)	0	1
V5BJY2	RanBP2-type domain-containing protein	TCDM_03227	Trypanosoma cruzi Dm28c	0	1

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