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 **276 - 300** 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 ▲
P01108	Myc proto-oncogene protein	Myc	Mus musculus (house mouse)	1	0	Burkitt lymphoma autosomal dominant polycystic kidney disease breast cancer hepatocellular carcinoma pancreatic carcinoma
P27797	Calreticulin	CALR CRTC	Homo sapiens (human)	4	39	Burkitt lymphoma colon cancer colon carcinoma esophagus squamous cell carcinoma essential thrombocythemia hepatocellular carcinoma lung adenocarcinoma lung cancer myelofibrosis neuroendocrine tumor pancreatic ductal adenocarcinoma sideroblastic anemia thrombocytosis
P83876	Thioredoxin-like protein 4A	DIM1 TXNL4 TXNL4A	Homo sapiens (human)	1	2	Burn-McKeown syndrome
Q9Y2U8	Inner nuclear membrane protein Man1	LEMD3 MAN1	Homo sapiens (human)	5	7	Buschke-Ollendorff syndrome
P40200	T-cell surface protein tactile	CD96	Homo sapiens (human)	15	1	C syndrome
Q61982	Neurogenic locus notch homolog protein 3	Notch3	Mus musculus (house mouse)	4	1	CADASIL 1 acute lymphoblastic leukemia
Q9UM47	Neurogenic locus notch homolog protein 3	NOTCH3	Homo sapiens (human)	18	9	CADASIL 1 infantile myofibromatosis lateral meningocele syndrome
P48552	Nuclear receptor-interacting protein 1	NRIP1	Homo sapiens (human)	2	1	CAKUT osteoporosis
Q3UKU5	Fibronectin type-III domain-containing protein	Lifr	Mus musculus (house mouse)	11	0	CAKUT
Q6XUX3	Dual serine/threonine and tyrosine protein kinase	DSTYK HDCMD38P KIAA0472 RIP5 RIPK5 SGK496	Homo sapiens (human)	1	1	CAKUT1 hereditary spastic paraplegia 23
P12644	Bone morphogenetic protein 4	BMP2B BMP4 DVR4	Homo sapiens (human)	4	0	CAKUT2 CAKUT atrial heart septal defect cartilage disease cleft lip melanoma orofacial cleft 11 ossification of the posterior longitudinal ligament of spine otosclerosis syndromic microphthalmia 6 tooth agenesis
P29965	CD40 ligand	CD40L CD40LG TNFSF5 TRAP	Homo sapiens (human)	1	32	CD40 ligand deficiency Graves' disease Kawasaki disease antiphospholipid syndrome autoimmune thrombocytopenic purpura combined T cell and B cell immunodeficiency coronary artery disease dysgammaglobulinemia follicular lymphoma human immunodeficiency virus infectious disease lupus nephritis multiple myeloma
Q9ERB0	Synaptosomal-associated protein 29	Snap29	Mus musculus (house mouse)	1	1	CEDNIK syndrome
O95721	Synaptosomal-associated protein 29	SNAP29	Homo sapiens (human)	5	2	CEDNIK syndrome
P02340	Cellular tumor antigen p53	P53 Tp53 Trp53	Mus musculus (house mouse)	1	0	CHARGE syndrome Li-Fraumeni syndrome breast cancer diffuse large B-cell lymphoma dyskeratosis congenita endometrial cancer glioblastoma osteosarcoma
B7Z002	Kismet, isoform C	136/31 2532 5841 BEST:GM02209 CG18326 CG3660 CG3696 DmelPex20 Dmel\CG3696 Dmel_CG3696 EC2-7 EK2-4 EP(2)0474 EP474 FBtr0078144 GM02209 KIS KIS-L Kis Kismet Pex20 Su(Pc)21AB anon-WO0172774.164 anon-WO0257455.5 kis kiss l(2)07812 l(2)k08827 l(2)k11324 l(2)k13631 l(2)k14112 l(2)k16510 l(2)s3527 l(2)s4771 l(2)s4793	Drosophila melanogaster (fruit fly)	6	0	CHARGE syndrome autism spectrum disorder congenital heart disease
Q9P2D1	Chromodomain-helicase-DNA-binding protein 7	CHD7 KIAA1416	Homo sapiens (human)	10	3	CHARGE syndrome hypogonadotropic hypogonadism 5 with or without anosmia
P36776	Lon protease homolog, mitochondrial	LONP1 PRSS15	Homo sapiens (human)	1	0	CODAS syndrome
P16442	Histo-blood group ABO system transferase	ABO	Homo sapiens (human)	1	0	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
Q14943	Killer cell immunoglobulin-like receptor 3DS1	KIR3DS1 NKAT10	Homo sapiens (human)	3	0	COVID-19 Polyomavirus-associated nephropathy West Nile fever acquired immunodeficiency syndrome chronic fatigue syndrome dengue hemorrhagic fever hepatitis B hepatitis C hepatocellular carcinoma human cytomegalovirus infection human immunodeficiency virus infectious disease liver cirrhosis lymphoproliferative syndrome malaria pulmonary tuberculosis syphilis tuberculosis
Q9NYK1	Toll-like receptor 7	TLR7 UNQ248/PRO285	Homo sapiens (human)	14	3	COVID-19 X-Linked immunodeficiency 74
P08603	Complement factor H	CFH HF HF1 HF2	Homo sapiens (human)	11	140	COVID-19 age related macular degeneration 4 anterior uveitis atypical hemolytic-uremic syndrome basal laminar drusen brain infarction cardiovascular system disease diabetic retinopathy hemolytic-uremic syndrome lupus nephritis macular degeneration panuveitis posterior uveitis retinal detachment retinal drusen sarcoidosis systemic lupus erythematosus
P10321	HLA class I histocompatibility antigen, C alpha chain	HLA-C HLAC	Homo sapiens (human)	5	7	COVID-19 allergic asthma human immunodeficiency virus infectious disease psoriasis 1
P08697	Alpha-2-antiplasmin	AAP PLI SERPINF2	Homo sapiens (human)	8	7	COVID-19 alpha-2-plasmin inhibitor deficiency
P05155	Plasma protease C1 inhibitor	C1IN C1NH SERPING1	Homo sapiens (human)	30	179	COVID-19 angioedema cerebral infarction hereditary angioedema type I hereditary angioedema macular degeneration pancreatitis toxic shock syndrome

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