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 **17951 - 17975** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q8N2N9	Ankyrin repeat domain-containing protein 36B	ANKRD36B	Homo sapiens (human)	2	1
Q3V0C3	NUT family member 2	Nutm2 Gm806	Mus musculus (house mouse)	1	1
Q03935	AP-1-like transcription factor YAP6	YAP6 HAL7	Saccharomyces cerevisiae S288C	3	1
Q91WC3	Long-chain-fatty-acid--CoA ligase 6	Acsl6 Facl6	Mus musculus (house mouse)	0	1
P0C881	Radial spoke head 10 homolog B	RSPH10B	Homo sapiens (human)	1	1
F6RQA2	Ribosomal protein S6 kinase	Rps6ka1	Mus musculus (house mouse)	0	1
Q3TBW2	Large ribosomal subunit protein uL10m	Mrpl10	Mus musculus (house mouse)	0	1
Q86X55	Histone-arginine methyltransferase CARM1	CARM1 PRMT4	Homo sapiens (human)	0	1
A0A8I5ZLS0	Vascular endothelial zinc finger 1	Vezf1	Rattus norvegicus (Norway rat)	0	1
Q8QZV2	Protein shisa-2 homolog	Shisa2 Shisa Tmem46	Mus musculus (house mouse)	1	1
Q5VUD6	Divergent protein kinase domain 1B	DIPK1B C9orf136 FAM69B	Homo sapiens (human)	2	1
A6NIV6	Leucine-rich repeat and IQ domain-containing protein 4	LRRIQ4 LRRC64	Homo sapiens (human)	2	1
Q86XR7	TIR domain-containing adapter molecule 2	TICAM2 TIRAP3 TIRP TRAM	Homo sapiens (human)	0	1
P50238	Cysteine-rich protein 1	CRIP1 CRIP CRP1	Homo sapiens (human)	0	1
P18754	Regulator of chromosome condensation	RCC1 CHC1	Homo sapiens (human)	2	1
Q96IV0	Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase	NGLY1 PNG1	Homo sapiens (human)	1	1	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
O00187	Mannan-binding lectin serine protease 2	MASP2	Homo sapiens (human)	1	1	B-cell lymphoma Burkitt lymphoma Chagas disease Crohn's colitis Crohn's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Kuhnt-Junius degeneration Langerhans-cell histiocytosis Stevens-Johnson syndrome Streptococcus pneumonia angioedema autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis cancer cardiac arrest cardiomyopathy cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chronic fatigue syndrome colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency cystic fibrosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma embryoma encephalomyelitis endomyocardial fibrosis erythema multiforme esophagus squamous cell carcinoma follicular lymphoma frontotemporal dementia glomerulonephritis hepatitis C hepatocellular carcinoma hereditary angioedema hypersensitivity reaction type III disease hypertrophic cardiomyopathy immune system disease inflammatory bowel disease 1 inflammatory bowel disease kidney disease large intestine cancer lepromatous leprosy leprosy liver cancer lymphoma malaria multiple sclerosis nephritis nephrosis non-Hodgkin lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ovarian cancer ovarian carcinoma parapsoriasis pneumonia psoriasis pustulosis of palm and sole pyoureter reticulosarcoma rheumatic fever rheumatoid arthritis sarcoidosis severe acute respiratory syndrome sporotrichosis systemic lupus erythematosus trypanosomiasis tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis urinary schistosomiasis viral infectious disease
Q00566	Methyl-CpG-binding protein 2	Mecp2	Rattus norvegicus (Norway rat)	9	1
Q8NDX6	Zinc finger protein 740	ZNF740 TB7	Homo sapiens (human)	0	1
P24534	Elongation factor 1-beta	EEF1B2 EEF1B EF1B	Homo sapiens (human)	0	1
Q5BJ29	F-box/LRR-repeat protein 7	Fbxl7 Kiaa0840	Mus musculus (house mouse)	1	1
Q8N9I0	Synaptotagmin-2	SYT2	Homo sapiens (human)	2	1
Q9QYG0	Protein NDRG2	Ndrg2 Kiaa1248 Ndr2	Mus musculus (house mouse)	0	1
P35762	CD81 antigen	Cd81 Tapa1	Mus musculus (house mouse)	1	1
O96827	Probable elongation factor 1-beta	eEF1beta	Drosophila melanogaster (fruit fly)	0	1

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