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 **3476 - 3500** 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
Q5VW38	Protein GPR107	GPR107 KIAA1624 LUSTR1	Homo sapiens (human)	6	17
P10767	Fibroblast growth factor 6	FGF6 HST2 HSTF2	Homo sapiens (human)	1	0
D2DKR8	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
R4N4F5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A1C3PHS8	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9UMR5	Lysosomal thioesterase PPT2	PPT2	Homo sapiens (human)	5	8	cancer cerebellar ataxia cerebellar disease embryoma histiocytosis membranous glomerulonephritis multiple myeloma multiple sclerosis neuroblastoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis
Q6P4I2	WD repeat-containing protein 73	WDR73	Homo sapiens (human)	0	1
Q9Y5H6	Protocadherin alpha-8	PCDHA8	Homo sapiens (human)	3	0
P29400	Collagen alpha-5(IV) chain	COL4A5	Homo sapiens (human)	4	1
Q02246	Contactin-2	CNTN2 AXT TAG1 TAX1	Homo sapiens (human)	13	5	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 B-cell lymphoma Gamstorp-Wohlfart syndrome Guillain-Barre syndrome Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Unverricht-Lundborg syndrome Van der Woude syndrome Wolff-Parkinson-White syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis adult T-cell leukemia/lymphoma adult lymphoma adult oligodendroglioma anaplastic astrocytoma arthritis arthropathy atrial fibrillation atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bladder carcinoma blepharospasm bone marrow disease bone osteosarcoma cancer central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood oligodendroglioma childhood osteosarcoma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy early myoclonic encephalopathy embryoma epilepsy episodic ataxia type 1 fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma immune system disease intellectual disability juvenile pilocytic astrocytoma keratoconjunctivitis sicca learning disability leukemia lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma microcephaly mixed glioma mixed oligodendroglioma-astrocytoma myotonic dystrophy type 2 neurodegenerative disease neurofibroma neurofibromatosis 1 neurofibromatosis neurogenic arthropathy obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma partial motor epilepsy peripheral nervous system neoplasm pilocytic astrocytoma primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma retinal vascular occlusion rheumatoid arthritis schizophrenia spinal cord disease subependymal giant cell astrocytoma syringomyelia systemic Epstein-Barr virus positive T-cell lymphoma of childhood tropical spastic paraparesis urinary bladder cancer visual epilepsy
A0A2I2MP54	Kallikrein-related peptidase 6 transcript variant 10	KLK6 Bssp Klk7 PRSS18 PRSS9 SP59 hK6	Homo sapiens (human)	1	0
O76013	Keratin, type I cuticular Ha6	KRT36 HHA6 HKA6 KRTHA6	Homo sapiens (human)	0	1
C1PHC3	CD44 molecule (Fragment)	CD44	Homo sapiens (human)	1	0
D6MKU2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8TDB8	Solute carrier family 2, facilitated glucose transporter member 14	SLC2A14 GLUT14	Homo sapiens (human)	5	2
J7F577	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q13936	Voltage-dependent L-type calcium channel subunit alpha-1C	CACNA1C CACH2 CACN2 CACNL1A1 CCHL1A1	Homo sapiens (human)	4	2
O00743	Serine/threonine-protein phosphatase 6 catalytic subunit	PPP6C PPP6	Homo sapiens (human)	1	1
Q8WWA0	Intelectin-1	ITLN1 INTL ITLN LFR	Homo sapiens (human)	1	0	Crohn's colitis Crohn's disease adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis bacterial infectious disease benign mesothelioma cancer carcinoma coronary artery disease cribriform carcinoma dermatitis diabetes mellitus diabetic ketoacidosis granular cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma malignant epithelial mesothelioma malignant mesothelioma multiple sclerosis neuroblastoma nutmeg liver obesity osteoporosis parapsoriasis pneumonia polycystic ovary syndrome primary biliary cholangitis psoriasis pustulosis of palm and sole sarcomatoid carcinoma stomach cancer stomach carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis
P41587	Vasoactive intestinal polypeptide receptor 2	VIPR2 VIP2R	Homo sapiens (human)	3	0
P62140	Serine/threonine-protein phosphatase PP1-beta catalytic subunit	PPP1CB	Homo sapiens (human)	0	1
Q6UXS0	C-type lectin domain family 19 member A	CLEC19A	Homo sapiens (human)	1	0
A0A090KFT5	HLA class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q06787	Fragile X messenger ribonucleoprotein 1	FMR1	Homo sapiens (human)	1	2
Q07075	Glutamyl aminopeptidase	ENPEP	Homo sapiens (human)	21	145

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