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 **13101 - 13125** 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
A0AVK6	Transcription factor E2F8	E2F8	Homo sapiens (human)	2	1
Q01826	DNA-binding protein SATB1	SATB1	Homo sapiens (human)	2	2
Q6IBE6	SIAT4C protein	SIAT4C ST3GAL4	Homo sapiens (human)	2	0
Q8N1G2	Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1	CMTR1 FTSJD2 KIAA0082 MTR1	Homo sapiens (human)	2	2
Q8NC56	LEM domain-containing protein 2	LEMD2	Homo sapiens (human)	2	10
G3XAL9	Solute carrier family 12 (Sodium/potassium/chloride transporters), member 2, isoform CRA_a	SLC12A2	Homo sapiens (human)	2	0
O75427	Leucine-rich repeat and calponin homology domain-containing protein 4	LRCH4 LRN LRRN1 LRRN4	Homo sapiens (human)	2	1
A0A0J9YXB8	Prosaposin (Fragment)	PSAP	Homo sapiens (human)	2	0
P28566	5-hydroxytryptamine receptor 1E	HTR1E	Homo sapiens (human)	2	0
Q6E0U4	Dermokine	DMKN	Homo sapiens (human)	2	1
Q9NRX5	Serine incorporator 1	SERINC1 KIAA1253 TDE1L TDE2	Homo sapiens (human)	2	2
Q9Y5H7	Protocadherin alpha-5	PCDHA5 CNRS6	Homo sapiens (human)	2	0
Q6T4P5	Phospholipid phosphatase-related protein type 3	PLPPR3 LPPR3 PHP2 PRG2	Homo sapiens (human)	2	0
P84098	Large ribosomal subunit protein eL19	RPL19	Homo sapiens (human)	2	2
Q7L3V2	Protein Bop	RTL10 BOP C22orf29	Homo sapiens (human)	2	1
Q8IV63	Serine/threonine-protein kinase VRK3	VRK3	Homo sapiens (human)	2	1
Q9BTE3	Mini-chromosome maintenance complex-binding protein	MCMBP C10orf119	Homo sapiens (human)	2	1
P08134	Rho-related GTP-binding protein RhoC	RHOC ARH9 ARHC	Homo sapiens (human)	2	1
P60891	Ribose-phosphate pyrophosphokinase 1	PRPS1	Homo sapiens (human)	2	1	Arts syndrome Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease type X Charcot-Marie-Tooth disease Foster-Kennedy syndrome Laron syndrome Werner syndrome X-linked nonsyndromic deafness achondroplasia acute lymphoblastic leukemia adult acute lymphocytic leukemia agenesis of the corpus callosum with peripheral neuropathy agnosia alternating exotropia anaplastic astrocytoma blindness breast cancer breast carcinoma cancer carcinoma central sleep apnea childhood acute lymphocytic leukemia childhood cerebral astrocytoma coloboma colorectal cancer colorectal carcinoma communication disorder congenital nystagmus critical illness polyneuropathy developmental coordination disorder diabetes insipidus disease of metabolism dissociated nystagmus embryoma epilepsy exotropia fibrillary astrocytoma fundus dystrophy gemistocytic astrocytoma giant cell glioblastoma glioblastoma gout hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperuricemia inflammatory and toxic neuropathy intellectual disability juvenile pilocytic astrocytoma kidney failure kwashiorkor language disorder large intestine cancer learning disability liver cancer locked-in syndrome malignant astrocytoma marasmus meningoencephalitis monocular exotropia motor peripheral neuropathy neuroblastoma neurodegeneration with brain iron accumulation neurohypophyseal diabetes insipidus neuropathy nutrition disease nutritional optic neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum optic atrophy optic nerve disease pancreas disease paraplegia pathologic nystagmus peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pilocytic astrocytoma placental insufficiency polyneuropathy primary immunodeficiency disease progeria protein-energy malnutrition protoplasmic astrocytoma quadriplegia sarcomatoid carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy spontaneous ocular nystagmus subependymal giant cell astrocytoma uric acid nephrolithiasis visual epilepsy visual pathway disease
Q15528	Mediator of RNA polymerase II transcription subunit 22	MED22 SURF5	Homo sapiens (human)	2	1
O14975	Long-chain fatty acid transport protein 2	SLC27A2 ACSVL1 FACVL1 FATP2 VLACS	Homo sapiens (human)	2	1
F5H125	Cell adhesion molecule 1 (Fragment)	CADM1	Homo sapiens (human)	2	0
Q9H222	ATP-binding cassette sub-family G member 5	ABCG5	Homo sapiens (human)	2	1
Q9Y5G9	Protocadherin gamma-A4	PCDHGA4	Homo sapiens (human)	2	0
Q8NGL0	Olfactory receptor 5L2	OR5L2	Homo sapiens (human)	2	0

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