GlyCosmos Portal

Source	Last Updated
GlyConnect	March 24, 2025
GlycoProtDB	December 4, 2018
GlyGen	October 30, 2024
The O-GlcNAc Database	January 30, 2025
UniProt	February 20, 2025

Displaying entries **176 - 200** of **139028** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
Q12948	Forkhead box protein C1	FKHL7 FOXC1 FREAC3	Homo sapiens (human)	9	3	Axenfeld-Rieger syndrome type 3 Axenfeld-Rieger syndrome anterior segment dysgenesis 3 glaucoma
P21275	Bone morphogenetic protein 4	Bmp-4 Bmp4 Dvr-4	Mus musculus (house mouse)	4	0	Axenfeld-Rieger syndrome type 3 atrioventricular septal defect cleft palate-lateral synechia syndrome fibrodysplasia ossificans progressiva physical disorder urinary system disease
P25440	Bromodomain-containing protein 2	BRD2 KIAA9001 RING3	Homo sapiens (human)	8	2	B-cell lymphoma B-lymphoblastic leukemia/lymphoma juvenile myoclonic epilepsy photosensitivity disease
Q9HBE5	Interleukin-21 receptor	IL21R NILR UNQ3121/PRO10273	Homo sapiens (human)	6	0	B-cell lymphoma Behcet's disease Crohn's disease common variable immunodeficiency diffuse large B-cell lymphoma human immunodeficiency virus infectious disease immunodeficiency 56 multiple sclerosis systemic lupus erythematosus temporal arteritis
P25942	Tumor necrosis factor receptor superfamily member 5	CD40 TNFRSF5	Homo sapiens (human)	2	27	B-cell lymphoma Burkitt lymphoma Crohn's disease Graves' disease Kawasaki disease arthritis asthma diffuse large B-cell lymphoma end stage renal disease follicular lymphoma hyperimmunoglobulin syndrome immunodeficiency with hyper IgM type 3 melanoma multiple myeloma multiple sclerosis non-Hodgkin lymphoma pancreatic ductal carcinoma pemphigus plasma cell leukemia psoriasis rheumatoid arthritis systemic lupus erythematosus
Q06187	Tyrosine-protein kinase BTK	AGMX1 ATK BPK BTK	Homo sapiens (human)	1	0	B-cell lymphoma Burkitt lymphoma X-linked agammaglobulinemia agammaglobulinemia central nervous system lymphoma isolated growth hormone deficiency type III mantle cell lymphoma
Q61188	Histone-lysine N-methyltransferase EZH2	Enx1h Ezh2	Mus musculus (house mouse)	1	0	B-cell lymphoma Weaver syndrome acute lymphoblastic leukemia
Q15910	Histone-lysine N-methyltransferase EZH2	EZH2 KMT6	Homo sapiens (human)	7	1	B-cell lymphoma Weaver syndrome acute megakaryocytic leukemia acute myeloid leukemia cholangiocarcinoma chronic myelomonocytic leukemia colorectal adenocarcinoma colorectal cancer congestive heart failure glioblastoma hepatocellular carcinoma lung cancer myelodysplastic syndrome myelofibrosis oral squamous cell carcinoma osteosarcoma renal Wilms' tumor stomach cancer
Q9UNQ0	Broad substrate specificity ATP-binding cassette transporter ABCG2	ABCG2 ABCP BCRP BCRP1 MXR	Homo sapiens (human)	1	0	B-cell lymphoma chronic myeloid leukemia gout multiple myeloma renal cell carcinoma toxic encephalopathy
P13726	Tissue factor	F3	Homo sapiens (human)	2	9	B-lymphoblastic leukemia/lymphoma COVID-19 disseminated intravascular coagulation von Willebrand's disease
P04637	Cellular tumor antigen p53	P53 TP53	Homo sapiens (human)	3	1	B-lymphoblastic leukemia/lymphoma Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome acute myeloid leukemia basal cell carcinoma breast cancer choroid plexus papilloma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis endometrial adenocarcinoma esophagus squamous cell carcinoma gastric adenocarcinoma hematologic cancer hepatocellular carcinoma high grade glioma low tension glaucoma melanoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome nasal cavity cancer nasopharynx carcinoma oral squamous cell carcinoma osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm papillary thyroid carcinoma paranasal sinus benign neoplasm primary open angle glaucoma prostate cancer sarcoma squamous cell carcinoma stomach cancer
P20815	Cytochrome P450 3A5	CYP3A5	Homo sapiens (human)	2	1	B-lymphoblastic leukemia/lymphoma acute lymphoblastic leukemia chronic myeloid leukemia essential hypertension
Q13422	DNA-binding protein Ikaros	IK1 IKAROS IKZF1 LYF1 ZNFN1A1	Homo sapiens (human)	3	2	B-lymphoblastic leukemia/lymphoma acute lymphoblastic leukemia colorectal cancer common variable immunodeficiency 13
P00519	Tyrosine-protein kinase ABL1	ABL ABL1 JTK7	Homo sapiens (human)	4	1	B-lymphoblastic leukemia/lymphoma acute myeloid leukemia chronic myeloid leukemia colorectal cancer esophagus adenocarcinoma oral squamous cell carcinoma
P10646	Tissue factor pathway inhibitor	LACI TFPI TFPI1	Homo sapiens (human)	9	45	B-lymphoblastic leukemia/lymphoma disseminated intravascular coagulation factor VIII deficiency liver cirrhosis myocardial infarction osteonecrosis protein S deficiency pulmonary fibrosis toxic shock syndrome transient cerebral ischemia
O75888	Tumor necrosis factor ligand superfamily member 13	APRIL TALL2 TNFSF13 UNQ383/PRO715 ZTNF2	Homo sapiens (human)	1	16	B-lymphoblastic leukemia/lymphoma
Q9C0F0	Putative Polycomb group protein ASXL3	ASXL3 KIAA1713	Homo sapiens (human)	12	1	Bainbridge-Ropers syndrome
O94761	ATP-dependent DNA helicase Q4	RECQ4 RECQL4	Homo sapiens (human)	3	1	Baller-Gerold syndrome Rothmund-Thomson syndrome rapadilino syndrome
P60484	Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN	MMAC1 PTEN TEP1	Homo sapiens (human)	1	1	Bannayan-Riley-Ruvalcaba syndrome Epstein-Barr virus infectious disease PTEN hamartoma tumor syndrome breast cancer esophageal cancer familial meningioma high grade glioma lung non-small cell carcinoma macrocephaly-autism syndrome ovarian cancer peripheral nervous system neoplasm prostate cancer sporadic breast cancer urinary bladder cancer
P60709	Actin, cytoplasmic 1	ACTB	Homo sapiens (human)	11	3	Baraitser-Winter syndrome 1 thrombocytopenia
P63261	Actin, cytoplasmic 2	ACTG ACTG1	Homo sapiens (human)	10	2	Baraitser-Winter syndrome 2 autosomal dominant nonsyndromic deafness 20
Q8WVJ9	Twist-related protein 2	BHLHA39 DERMO1 TWIST2	Homo sapiens (human)	3	1	Barber-Say syndrome ablepharon macrostomia syndrome
Q5HYA8	Meckelin	MKS3 TMEM67	Homo sapiens (human)	4	2	Bardet-Biedl syndrome 14 Bardet-Biedl syndrome COACH syndrome Joubert syndrome 6 Meckel syndrome 3 coloboma nephronophthisis 11 nephronophthisis portal hypertension
Q9BXC9	BBSome complex member BBS2	BBS2	Homo sapiens (human)	1	1	Bardet-Biedl syndrome 2 Bardet-Biedl syndrome obesity retinitis pigmentosa 74
Q96LB3	Intraflagellar transport protein 74 homolog	CCDC2 CMG1 IFT74	Homo sapiens (human)	2	2	Bardet-Biedl syndrome 22 Joubert syndrome spermatogenic failure 58

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