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 **5426 - 5450** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8N0V5	N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase	GCNT2 GCNT5 II NACGT1	Homo sapiens (human)	2	2	abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma esophagus squamous cell carcinoma gallbladder cancer gallbladder carcinoma hyperferritinemia-cataract syndrome kidney failure large intestine cancer melanoma skin melanoma tuberculosis uremia
B4DU55	Zinc finger protein 879	ZNF879	Homo sapiens (human)	0	1
Q9BZG2	Testicular acid phosphatase	ACP4 ACPT	Homo sapiens (human)	4	0
A0A2I6Q794	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q8N264	Rho GTPase-activating protein 24	ARHGAP24 FILGAP	Homo sapiens (human)	1	1
Q9H0P0	Cytosolic 5'-nucleotidase 3A	NT5C3A NT5C3 P5N1 UMPH1	Homo sapiens (human)	0	1
Q6P0N0	Mis18-binding protein 1	MIS18BP1 C14orf106 KIAA1903 KNL2 M18BP1	Homo sapiens (human)	1	1
A0A2I6PN80	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
F5H1E8	Alpha-2-macroglobulin	A2M	Homo sapiens (human)	2	0
Q86U06	Probable RNA-binding protein 23	RBM23 RNPC4	Homo sapiens (human)	0	1
A0A1B0GU74	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
C9WCV6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A6Q8PFA9	Alpha-galactosidase	GLA	Homo sapiens (human)	2	0
Q05D91	Hypoxia up-regulated protein 1 (Fragment)	HYOU1	Homo sapiens (human)	2	0
Q8N6L6	C3/C5 convertase	C2	Homo sapiens (human)	1	0
C9WCR1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P56524	Histone deacetylase 4	HDAC4 KIAA0288	Homo sapiens (human)	4	1
A0A0N7A4C9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
G1EPU3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q6IN85	Serine/threonine-protein phosphatase 4 regulatory subunit 3A	PPP4R3A KIAA2010 PP4R3A SMEK1	Homo sapiens (human)	0	1
Q7L5Y1	Mitochondrial enolase superfamily member 1	ENOSF1 RTS TYMSAS	Homo sapiens (human)	0	1	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
A0A7P0TBJ5	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Homo sapiens (human)	2	0
A0A0G3EHL4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9HBG7	T-lymphocyte surface antigen Ly-9	LY9	Homo sapiens (human)	12	3
Q9H479	Fructosamine-3-kinase	FN3K	Homo sapiens (human)	0	1

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