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 **4376 - 4400** 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
Q8WXF0	Serine/arginine-rich splicing factor 12	SRSF12 SFRS13B SFRS19 SRRP35	Homo sapiens (human)	1	1
A0A1C3PHE1	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
P78551	PERB11.1 protein (Fragment)	PERB11.1	Homo sapiens (human)	1	0
P59551	Taste receptor type 2 member 60	TAS2R60	Homo sapiens (human)	1	0
J7K040	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P54198	Protein HIRA	HIRA DGCR1 HIR TUPLE1	Homo sapiens (human)	5	1
G3D6J9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P22061	Protein-L-isoaspartate(D-aspartate) O-methyltransferase	PCMT1	Homo sapiens (human)	2	2
Q8WXG9	Adhesion G-protein coupled receptor V1	ADGRV1 GPR98 KIAA0686 KIAA1943 MASS1 VLGR1	Homo sapiens (human)	34	12
M0QY31	Pregnancy specific beta-1-glycoprotein 4 (Fragment)	PSG4	Homo sapiens (human)	2	0
Q96FT7	Acid-sensing ion channel 4	ASIC4 ACCN4	Homo sapiens (human)	3	0
Q969N2	GPI transamidase component PIG-T	PIGT	Homo sapiens (human)	5	16	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
Q5VVC0	Protein SPO16 homolog	SPO16 C1orf146 SCRE	Homo sapiens (human)	1	1
P55001	Microfibrillar-associated protein 2	MFAP2 MAGP1	Homo sapiens (human)	2	2
Q8IXQ9	Electron transfer flavoprotein beta subunit lysine methyltransferase	ETFBKMT C12orf72 METTL20	Homo sapiens (human)	0	1
Q08397	Lysyl oxidase homolog 1	LOXL1 LOXL	Homo sapiens (human)	1	1
A0A2I8B366	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
P52798	Ephrin-A4	EFNA4 EPLG4 LERK4	Homo sapiens (human)	2	5
Q8IV08	5'-3' exonuclease PLD3	PLD3	Homo sapiens (human)	6	37	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 Henoch-Schoenlein purpura Pick's disease Reye syndrome amyloidosis atopic dermatitis cerebral degeneration congenital nystagmus conjunctival folliculosis conjunctivitis dermatitis dissociated nystagmus hypersensitivity vasculitis keratitis keratoconjunctivitis pathologic nystagmus rheumatoid arthritis scleroderma shipyard eye spinocerebellar ataxia 46 spontaneous ocular nystagmus systemic scleroderma
Q96GY3	Protein lin-37 homolog	LIN37	Homo sapiens (human)	0	1
Q8WUI4	Histone deacetylase 7	HDAC7 HDAC7A	Homo sapiens (human)	0	1
A0A5H2V1T5	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q8NFJ6	Prokineticin receptor 2	PROKR2 GPR73L1 PKR2	Homo sapiens (human)	2	0
A0A7I2V4D1	Carboxypeptidase	CTSA	Homo sapiens (human)	1	0
Q96K80	Zinc finger CCCH domain-containing protein 10	ZC3H10 ZC3HDC10	Homo sapiens (human)	0	1

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