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 **2401 - 2425** 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
Q6ZSZ6	Teashirt homolog 1	TSHZ1 SDCCAG33 TSH1	Homo sapiens (human)	3	2
P01701	Immunoglobulin lambda variable 1-51	IGLV1-51	Homo sapiens (human)	0	1
J7K1A7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
D2DKR3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
B8ZZ34	Protein shisa-8	SHISA8 C22orf17	Homo sapiens (human)	1	0
O14827	Ras-specific guanine nucleotide-releasing factor 2	RASGRF2 GRF2	Homo sapiens (human)	2	1
H0Y300	Haptoglobin	HP	Homo sapiens (human)	4	0
P78352	Disks large homolog 4	DLG4 PSD95	Homo sapiens (human)	0	1
P52209	6-phosphogluconate dehydrogenase, decarboxylating	PGD PGDH	Homo sapiens (human)	1	1	46,XY sex reversal 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 Down syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Leber hereditary optic neuropathy Leigh disease Marfan syndrome Meckel syndrome 3 Meckel syndrome Pick's disease Plasmodium vivax malaria Reye syndrome Turner syndrome adenocarcinoma adenoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia androgen insensitivity syndrome asthma atopic dermatitis autosomal dominant polycystic kidney disease azoospermia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia cribriform carcinoma cutaneous leishmaniasis cystic fibrosis depressive disorder dermatitis disorder of sexual development dysgerminoma dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fragile X syndrome gonadal dysgenesis gonadoblastoma granular cell carcinoma hemoglobin H disease hepatocellular carcinoma hermaphroditism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma major depressive disorder malaria melancholic depression microcephaly microphthalmia mixed gonadal dysgenesis mood disorder myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neurofibromatosis 1 neurofibromatosis neurotic disorder obsolete Matthew-Wood syndrome obsolete melancholia polycystic kidney disease 1 premature menopause pseudohermaphroditism seminoma situs inversus squamous cell carcinoma testicular cancer testicular germ cell cancer testis seminoma thalassemia thyroid gland anaplastic carcinoma tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma ulcerative colitis vitiligo
Q86UZ1	CD44 antigen	CD44	Homo sapiens (human)	1	0
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	Homo sapiens (human)	13	12	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
Q9UI47	Catenin alpha-3	CTNNA3	Homo sapiens (human)	1	1
A0A7I2V4V1	Peptidyl-prolyl cis-trans isomerase	PPIA	Homo sapiens (human)	1	0
A0A140T986	MHC class I polypeptide-related sequence A	MICA	Homo sapiens (human)	1	0
A0A383S2H1	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q5T750	Protein KPLCE	KPLCE C1orf68 LEP7 XP32	Homo sapiens (human)	0	1
O75592	E3 ubiquitin-protein ligase MYCBP2	MYCBP2 KIAA0916 PAM	Homo sapiens (human)	8	3
K7P5I1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9H422	Homeodomain-interacting protein kinase 3	HIPK3 DYRK6 FIST3 PKY	Homo sapiens (human)	1	1
P62987	Ubiquitin-ribosomal protein eL40 fusion protein	UBA52 UBCEP2	Homo sapiens (human)	1	1
O15344	E3 ubiquitin-protein ligase Midline-1	MID1 FXY RNF59 TRIM18 XPRF	Homo sapiens (human)	1	2
F8SKX1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
O95782	AP-2 complex subunit alpha-1	AP2A1 ADTAA CLAPA1	Homo sapiens (human)	3	2
Q1MSJ5	Centrosome and spindle pole-associated protein 1	CSPP1 CSPP	Homo sapiens (human)	0	1
Q9H307	Pinin	PNN DRS MEMA	Homo sapiens (human)	1	1

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