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 **13576 - 13600** 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
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
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
Q8N9I0	Synaptotagmin-2	SYT2	Homo sapiens (human)	2	1
Q16778	Histone H2B type 2-E	H2BC21 H2BFQ HIST2H2BE	Homo sapiens (human)	1	1
Q07866	Kinesin light chain 1	KLC1 KLC KNS2	Homo sapiens (human)	0	1
O60488	Long-chain-fatty-acid--CoA ligase 4	ACSL4 ACS4 FACL4 LACS4	Homo sapiens (human)	3	1	Alport syndrome Bell's palsy Duchenne muscular dystrophy Meckel's diverticulum abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder bacterial sepsis bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer clubfoot colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hemolytic anemia cribriform carcinoma depressive disorder disease of mental health dysthymic disorder embryoma epithelioid leiomyosarcoma epithelioid sarcoma facial nerve disease facial paralysis favism follicular adenoma generalized anxiety disorder gliosarcoma glomerulonephritis granular cell carcinoma granuloma annulare hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypertropia intellectual disability kidney failure large intestine cancer learning disability leiomyosarcoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder mechanical strabismus melancholic depression microcystic adenoma mixed glioma muscular dystrophy myopia myxoid leiomyosarcoma nephritis neuromuscular disease neurotic disorder non-syndromic X-linked intellectual disability obesity obsolete melancholia ophthalmoplegia osteoarthritis papillary adenoma patent ductus arteriosus placental insufficiency prostate cancer prostate carcinoma proteinuria psychotic disorder pyloric stenosis sarcoma schizophrenia sensorineural hearing loss spindle cell sarcoma steatotic liver disease stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 systemic lupus erythematosus tubular adenocarcinoma visual epilepsy
Q9NWS1	PCNA-interacting partner	PARPBP C12orf48 PARI	Homo sapiens (human)	0	1
Q7Z407	CUB and sushi domain-containing protein 3	CSMD3 KIAA1894	Homo sapiens (human)	44	1
Q96HA1	Nuclear envelope pore membrane protein POM 121	POM121 KIAA0618 NUP121 POM121A	Homo sapiens (human)	25	1
Q9Y3B7	Large ribosomal subunit protein uL11m	MRPL11	Homo sapiens (human)	0	1
Q5T6S3	PHD finger protein 19	PHF19 PCL3	Homo sapiens (human)	0	1
Q8IVV7	Glucose-induced degradation protein 4 homolog	GID4 C17orf39 VID24	Homo sapiens (human)	3	1
Q96FG2	ELMO domain-containing protein 3	ELMOD3 RBED1 RBM29	Homo sapiens (human)	0	1
E9PAV3	Nascent polypeptide-associated complex subunit alpha, muscle-specific form	NACA	Homo sapiens (human)	16	1
Q96NW4	Ankyrin repeat domain-containing protein 27	ANKRD27	Homo sapiens (human)	0	1
P49720	Proteasome subunit beta type-3	PSMB3	Homo sapiens (human)	0	1
Q9P0M9	Large ribosomal subunit protein bL27m	MRPL27	Homo sapiens (human)	0	1
Q6ZU35	Capping protein-inhibiting regulator of actin dynamics	CRACD CRAD KIAA1211	Homo sapiens (human)	0	1
Q16633	POU domain class 2-associating factor 1	POU2AF1 BOB1 OBF1	Homo sapiens (human)	1	1

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