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 **17876 - 17900** 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
A0A514TNJ1	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q2M3D2	Exocyst complex component 3-like protein 2	EXOC3L2 XTP7	Homo sapiens (human)	0	1
Q8WXS5	Voltage-dependent calcium channel gamma-8 subunit	CACNG8 CACNG6	Homo sapiens (human)	2	1
F2VNP3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
G0Z8C9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
D6R9S8	Claudin domain containing 1 (Fragment)	CLDND1	Homo sapiens (human)	1	0
Q6UQ28	Placenta-expressed transcript 1 protein	PLET1 C11orf34	Homo sapiens (human)	2	0	cancer embryoma
Q96GM1	Phospholipid phosphatase-related protein type 2	PLPPR2 LPPR2 PRG4	Homo sapiens (human)	1	0
Q9P0K7	Ankycorbin	RAI14 KIAA1334 NORPEG	Homo sapiens (human)	5	4
K7ES75	Galectin 3 binding protein (Fragment)	LGALS3BP	Homo sapiens (human)	1	0
P02545	Prelamin-A/C	LMNA LMN1	Homo sapiens (human)	28	2
Q14439	G-protein coupled receptor 176	GPR176	Homo sapiens (human)	4	0
M1PIT1	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
Q96N87	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	SLC6A18 B0AT3 XTRP2	Homo sapiens (human)	4	0
O75556	Mammaglobin-B	SCGB2A1 LIPHC MGB2 UGB3	Homo sapiens (human)	1	2
A0A2I6PN74	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
D7NP14	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9UP83	Conserved oligomeric Golgi complex subunit 5	COG5 GOLTC1 GTC90	Homo sapiens (human)	1	2	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 Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy
D2DKH1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P00797	Renin	REN	Homo sapiens (human)	2	32
Q5VZE5	N-alpha-acetyltransferase 35, NatC auxiliary subunit	NAA35 EGAP MAK10	Homo sapiens (human)	2	1
A0A6C0SGN1	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
P09172	Dopamine beta-hydroxylase	DBH	Homo sapiens (human)	4	12
A0A1B0GTM3	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0
Q96IZ0	PRKC apoptosis WT1 regulator protein	PAWR PAR4	Homo sapiens (human)	12	1

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