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
Q96G61	Diphosphoinositol polyphosphate phosphohydrolase 3-beta	NUDT11 APS1 DIPP3B	Homo sapiens (human)	0	1
Q96G46	tRNA-dihydrouridine(47) synthase [NAD(P)(+)]-like	DUS3L	Homo sapiens (human)	0	1
Q96G42	Kelch domain-containing protein 7B	KLHDC7B	Homo sapiens (human)	1	1
Q96G30	Melanocortin-2 receptor accessory protein 2	MRAP2 C6orf117	Homo sapiens (human)	1	0
Q96G28	Cilia- and flagella-associated protein 36	CFAP36 CCDC104	Homo sapiens (human)	1	1
Q96G27	WW domain-binding protein 1	WBP1	Homo sapiens (human)	1	0
Q96G25	Mediator of RNA polymerase II transcription subunit 8	MED8	Homo sapiens (human)	0	1
Q96G23	Ceramide synthase 2	CERS2 LASS2 TMSG1	Homo sapiens (human)	3	33	bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chronic fatigue syndrome chronic kidney disease colitis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis gastroenteritis giant cell glioblastoma glioblastoma heart disease high grade glioma hyperglycemia ileitis ileocolitis inflammatory bowel disease melanoma multiple sclerosis myelitis papillary adenocarcinoma papillary renal cell carcinoma primary cutaneous amyloidosis prostate cancer prostate carcinoma sarcomatoid carcinoma skin melanoma steatotic liver disease thyroid gland papillary carcinoma type 2 diabetes mellitus urinary bladder cancer
Q96G21	U3 small nucleolar ribonucleoprotein protein IMP4	IMP4 BXDC4	Homo sapiens (human)	0	1
Q96G04	Protein-lysine N-methyltransferase EEF2KMT	EEF2KMT FAM86A	Homo sapiens (human)	1	1
Q96G03	Phosphopentomutase	PGM2	Homo sapiens (human)	0	1
Q96FZ2	Abasic site processing protein HMCES	HMCES C3orf37 DC12 SRAPD1	Homo sapiens (human)	1	2
Q96FX7	tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A	TRMT61A C14orf172 TRM61	Homo sapiens (human)	0	1
Q96FW1	Ubiquitin thioesterase OTUB1	OTUB1 OTB1 OTU1	Homo sapiens (human)	0	1
Q96FV9	THO complex subunit 1	THOC1 HPR1	Homo sapiens (human)	1	2
Q96FV3	Tetraspanin-17	TSPAN17 FBXO23 TM4SF17	Homo sapiens (human)	2	0
Q96FV0	Leucine-rich repeat-containing protein 46	LRRC46	Homo sapiens (human)	4	1
Q96FT7	Acid-sensing ion channel 4	ASIC4 ACCN4	Homo sapiens (human)	3	0
Q96FS4	Signal-induced proliferation-associated protein 1	SIPA1 SPA1	Homo sapiens (human)	0	1
Q96FQ6	Protein S100-A16	S100A16 S100F	Homo sapiens (human)	0	1
Q96FN5	Kinesin-like protein KIF12	KIF12	Homo sapiens (human)	0	1
Q96FN4	Copine-2	CPNE2	Homo sapiens (human)	0	1
Q96FM1	Post-GPI attachment to proteins factor 3	PGAP3 CAB2 PERLD1	Homo sapiens (human)	1	7	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
Q96FL9	Polypeptide N-acetylgalactosaminyltransferase 14	GALNT14	Homo sapiens (human)	3	3	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
Q96FJ2	Dynein light chain 2, cytoplasmic	DYNLL2 DLC2	Homo sapiens (human)	0	1

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