GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **1851 - 1875** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q8IWU9	Tryptophan 5-hydroxylase 2	TPH2 NTPH	Homo sapiens (human)	1
Q15669	Rho-related GTP-binding protein RhoH	RHOH ARHH TTF	Homo sapiens (human)	1
O60762	Dolichol-phosphate mannosyltransferase subunit 1	DPM1	Homo sapiens (human)	1	Duchenne muscular dystrophy antithrombin III deficiency autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 capillary disease cavernous hemangioma chorioangioma congenital disorder of glycosylation Ie congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy glomus tumor hemangioma hereditary hemorrhagic telangiectasia histiocytoid hemangioma intramuscular hemangioma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lymphangioma microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nonsyndromic congenital nail disorder 9 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 patent ductus arteriosus protein C deficiency protein S deficiency rippling muscle disease 2 telangiectasis thrombophilia
Q9H2V7	Protein spinster homolog 1	SPNS1 SPIN1	Homo sapiens (human)	1
A6NKD2	Testis-specific Y-encoded protein 2	TSPY2 TSPYQ1	Homo sapiens (human)	1
O15258	Protein RER1	RER1	Homo sapiens (human)	1
Q8IYK8	GTP-binding protein REM 2	REM2	Homo sapiens (human)	1
Q9NQE9	Adenosine 5'-monophosphoramidase HINT3	HINT3	Homo sapiens (human)	1
Q6YN16	Hydroxysteroid dehydrogenase-like protein 2	HSDL2 C9orf99 SDR13C1	Homo sapiens (human)	1
Q9H0D2	Zinc finger protein 541	ZNF541	Homo sapiens (human)	1
P23025	DNA repair protein complementing XP-A cells	XPA XPAC	Homo sapiens (human)	1
Q67FW5	Queuosine-tRNA galactosyltransferase	B3GNTL1 B3GNT8 QTGAL	Homo sapiens (human)	1	bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole
Q2M1K9	Zinc finger protein 423	ZNF423 KIAA0760 NPHP14 OAZ	Homo sapiens (human)	1
P61626	Lysozyme C	LYZ LZM	Homo sapiens (human)	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 Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Graves' disease Langerhans-cell histiocytosis Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome Shwachman-Diamond syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acinar cell carcinoma acne acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia adenocarcinoma adenoid cystic carcinoma adenoma alcohol dependence alcohol use disorder allergic rhinitis alternating hemiplegia of childhood amyloidosis anorexia nervosa aphthous stomatitis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autonomic neuropathy bacterial infectious disease bacterial vaginosis biliary tract disease breast cancer breast carcinoma cancer candidiasis celiac disease central nervous system cancer central nervous system disease cerebral degeneration childhood leukemia cholestasis chronic ethmoiditis chronic monocytic leukemia chronic myelomonocytic leukemia chronic sphenoidal sinusitis colitis common cold complement deficiency congestive heart failure coronary artery disease craniosynostosis cribriform carcinoma dacryoadenitis dacryocystitis diabetes mellitus diabetic ketoacidosis diarrhea dysentery egg allergy endocrine exophthalmos essential hypertension exanthem familial hyperlipidemia familial mediterranean fever familial nephrotic syndrome familial visceral amyloidosis follicular adenoma gallbladder disease gastritis gastroduodenal Crohn's disease gastroenteritis gastrointestinal stromal tumor gastrointestinal system disease gingivitis gliosarcoma glomerulonephritis granular cell carcinoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hyperthyroidism hypohidrotic ectodermal dysplasia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease intestinal disease intestinal infectious disease jejunoileitis juvenile myelomonocytic leukemia juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure leukemia lipoid nephrosis liver cancer liver disease malignant fibrous histiocytoma mastitis meningitis mevalonic aciduria microcystic adenoma mixed glioma myeloid sarcoma nephritis nephrosis nephrotic syndrome nervous system disease neuropathy nodular prostate non-Langerhans-cell histiocytosis obsolete malignant histiocytosis obsolete ymphosarcoma obstructive jaundice oral candidiasis oral mucosa leukoplakia papillary adenoma parapsoriasis periodontal disease peripheral nervous system disease polyneuropathy post-traumatic stress disorder proctitis prostatic adenoma proteinuria psoriasis pulmonary tuberculosis purpura pustulosis of palm and sole pyoureter reticulohistiocytic granuloma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoidosis seborrheic keratosis shigellosis sickle cell anemia skin disease spiradenoma stomach cancer stomach carcinoma systemic lupus erythematosus thyrotoxicosis tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia ureteral obstruction uveoparotid fever vaginitis vasomotor rhinitis vulvitis vulvovaginitis white sponge nevus
Q5VW32	BRO1 domain-containing protein BROX	BROX BROFTI C1orf58	Homo sapiens (human)	1
Q9NPJ6	Mediator of RNA polymerase II transcription subunit 4	MED4 ARC36 DRIP36 VDRIP	Homo sapiens (human)	1
P68036	Ubiquitin-conjugating enzyme E2 L3	UBE2L3 UBCE7 UBCH7	Homo sapiens (human)	1
O75832	26S proteasome non-ATPase regulatory subunit 10	PSMD10	Homo sapiens (human)	1	B-cell lymphoma T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult cystic teratoma adult teratoma autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma childhood testicular germ cell tumor cholangiocarcinoma cholesteatoma of middle ear cholesteatoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cystic teratoma dedifferentiated liposarcoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis ehrlichiosis embryoma embryonal cancer embryonal carcinoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial retinoblastoma follicular adenoma gastroenteritis germ cell and embryonal cancer germ cell cancer germinoma gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease inflammatory bowel disease influenza intrahepatic cholangiocarcinoma invasive ductal carcinoma islet cell tumor large intestine cancer liposarcoma liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma malignant teratoma mature teratoma melanoma microcystic adenoma mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction myopia nonpapillary renal cell carcinoma normal pressure hydrocephalus obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma pleomorphic liposarcoma polyp of middle ear prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma retinopathy of prematurity sarcomatoid renal cell carcinoma schizophrenia seminoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratoma testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thymic carcinoma thymoma tongue squamous cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine corpus cancer viral infectious disease visual epilepsy
Q8N157	Jouberin	AHI1	Homo sapiens (human)	1
Q99816	Tumor susceptibility gene 101 protein	TSG101	Homo sapiens (human)	1
P62891	Large ribosomal subunit protein eL39	RPL39	Homo sapiens (human)	1
P41223	Protein BUD31 homolog	BUD31 EDG2	Homo sapiens (human)	1
Q96SZ5	2-aminoethanethiol dioxygenase	ADO C10orf22	Homo sapiens (human)	1
Q86WX3	Active regulator of SIRT1	RPS19BP1 AROS	Homo sapiens (human)	1
Q7Z4L5	Tetratricopeptide repeat protein 21B	TTC21B IFT139 KIAA1992	Homo sapiens (human)	1

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