GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **2826 - 2850** 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
Q9BTC8	Metastasis-associated protein MTA3	MTA3 KIAA1266	Homo sapiens (human)	0	1
Q9BTC0	Death-inducer obliterator 1	DIDO1 C20orf158 DATF1 KIAA0333	Homo sapiens (human)	32	2
Q9BTA9	WW domain-containing adapter protein with coiled-coil	WAC KIAA1844	Homo sapiens (human)	11	1
Q9BT81	Transcription factor SOX-7	SOX7	Homo sapiens (human)	0	1
Q9BT78	COP9 signalosome complex subunit 4	COPS4 CSN4	Homo sapiens (human)	1	2
Q9BT76	Uroplakin-3b	UPK3B	Homo sapiens (human)	1	0
Q9BT73	Proteasome assembly chaperone 3	PSMG3 C7orf48 PAC3	Homo sapiens (human)	0	1
Q9BT30	Alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial	ALKBH7 ABH7 SPATA11	Homo sapiens (human)	0	1
Q9BT25	HAUS augmin-like complex subunit 8	HAUS8 HICE1	Homo sapiens (human)	0	1
Q9BT22	Chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 HMAT1 HMT1	Homo sapiens (human)	0	1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
Q9BT09	Protein canopy homolog 3	CNPY3 CTG4A ERDA5 PRAT4A TNRC5	Homo sapiens (human)	6	14
Q9BT04	Protein fuzzy homolog	FUZ FY	Homo sapiens (human)	1	1
Q9BSV6	tRNA-splicing endonuclease subunit Sen34	TSEN34 LENG5 SEN34	Homo sapiens (human)	0	1
Q9BSQ5	Cerebral cavernous malformations 2 protein	CCM2 C7orf22	Homo sapiens (human)	2	1
Q9BSN7	Transmembrane protein 204	TMEM204 C16orf30 CLP24	Homo sapiens (human)	1	0
Q9BSL1	Ubiquitin-associated domain-containing protein 1	UBAC1 GBDR1 KPC2 UBADC1	Homo sapiens (human)	1	2
Q9BSK2	Solute carrier family 25 member 33	SLC25A33	Homo sapiens (human)	0	1
Q9BSJ8	Extended synaptotagmin-1	ESYT1 FAM62A KIAA0747 MBC2	Homo sapiens (human)	2	2
Q9BSJ6	Protein PIMREG	PIMREG CATS FAM64A RCS1	Homo sapiens (human)	0	1
Q9BSJ2	Gamma-tubulin complex component 2	TUBGCP2 GCP2	Homo sapiens (human)	1	1
Q9BSH4	Translational activator of cytochrome c oxidase 1	TACO1 CCDC44	Homo sapiens (human)	1	1
Q9BSG0	Protease-associated domain-containing protein 1	PRADC1 C2orf7 PAP21	Homo sapiens (human)	1	0
Q9BSF8	BTB/POZ domain-containing protein 10	BTBD10 GMRP1	Homo sapiens (human)	0	1
Q9BSD7	Cancer-related nucleoside-triphosphatase	NTPCR C1orf57	Homo sapiens (human)	0	1
Q9BSA4	Protein tweety homolog 2	TTYH2 C17orf29	Homo sapiens (human)	4	0

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