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 **3551 - 3575** 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
Q8N0T1	Ribosomal biogenesis factor	RBIS C8orf59	Homo sapiens (human)	0	1
O43159	Ribosomal RNA-processing protein 8	RRP8 KIAA0409 NML	Homo sapiens (human)	3	1
Q92979	Ribosomal RNA small subunit methyltransferase NEP1	EMG1 C2F	Homo sapiens (human)	0	1
Q14684	Ribosomal RNA processing protein 1 homolog B	RRP1B KIAA0179	Homo sapiens (human)	10	1
P56182	Ribosomal RNA processing protein 1 homolog A	RRP1 D21S2056E NNP1 NOP52 RRP1A	Homo sapiens (human)	0	1
O76021	Ribosomal L1 domain-containing protein 1	RSL1D1 CATX11 CSIG PBK1	Homo sapiens (human)	4	1
P21108	Ribose-phosphate pyrophosphokinase 3	PRPS1L1 PRPS3 PRPSL	Homo sapiens (human)	1	1
P11908	Ribose-phosphate pyrophosphokinase 2	PRPS2	Homo sapiens (human)	1	1	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus
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
P49247	Ribose-5-phosphate isomerase	RPIA RPI	Homo sapiens (human)	2	1	Chagas disease agnosia cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus critical illness polyneuropathy disease of metabolism dissociated nystagmus epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis hepatocellular carcinoma inflammatory and toxic neuropathy islet cell tumor large intestine cancer liver cancer liver carcinoma meningoencephalitis multiple myeloma neuropathy optic atrophy papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease polyneuropathy spontaneous ocular nystagmus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma trypanosomiasis visual epilepsy
Q7LG56	Ribonucleoside-diphosphate reductase subunit M2 B	RRM2B P53R2	Homo sapiens (human)	0	1
P31350	Ribonucleoside-diphosphate reductase subunit M2	RRM2 RR2	Homo sapiens (human)	0	1
P23921	Ribonucleoside-diphosphate reductase large subunit	RRM1 RR1	Homo sapiens (human)	6	1
Q8IY67	Ribonucleoprotein PTB-binding 1	RAVER1 KIAA1978	Homo sapiens (human)	0	1
Q99575	Ribonucleases P/MRP protein subunit POP1	POP1 KIAA0061	Homo sapiens (human)	3	2
P07998	Ribonuclease pancreatic	RNASE1 RIB1 RNS1	Homo sapiens (human)	3	3
P13489	Ribonuclease inhibitor	RNH1 PRI RNH	Homo sapiens (human)	0	1
D6RHI9	Ribonuclease T2 (Fragment)	RNASET2	Homo sapiens (human)	3	0
A0A087WWI1	Ribonuclease T2	RNASET2	Homo sapiens (human)	1	0
A0A087WZM2	Ribonuclease T2	RNASET2	Homo sapiens (human)	3	0
D6REQ6	Ribonuclease T2	RNASET2	Homo sapiens (human)	3	0
O00584	Ribonuclease T2	RNASET2 RNASE6PL	Homo sapiens (human)	4	24
Q969H6	Ribonuclease P/MRP protein subunit POP5	POP5	Homo sapiens (human)	0	1
P78345	Ribonuclease P protein subunit p38	RPP38	Homo sapiens (human)	0	1
P78346	Ribonuclease P protein subunit p30	RPP30 RNASEP2	Homo sapiens (human)	0	1

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