GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
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Displaying entries **12876 - 12900** 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
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
Q96FG2	ELMO domain-containing protein 3	ELMOD3 RBED1 RBM29	Homo sapiens (human)	0	1
Q96FF9	Sororin	CDCA5	Homo sapiens (human)	0	1
Q96FF7	Uncharacterized protein MISP3	MISP3	Homo sapiens (human)	2	1
Q96FE7	Phosphoinositide-3-kinase-interacting protein 1	PIK3IP1 HGFL	Homo sapiens (human)	6	20
Q96FE5	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1	LINGO1 LERN1 LRRN6A	Homo sapiens (human)	10	3
Q96FC7	Phytanoyl-CoA hydroxylase-interacting protein-like	PHYHIPL KIAA1796	Homo sapiens (human)	3	1
Q96F86	Enhancer of mRNA-decapping protein 3	EDC3 LSM16 YJDC YJEFN2	Homo sapiens (human)	2	1
Q96F81	Protein dispatched homolog 1	DISP1 DISPA	Homo sapiens (human)	2	0
Q96F63	Coiled-coil domain-containing protein 97	CCDC97	Homo sapiens (human)	0	1
Q96F46	Interleukin-17 receptor A	IL17RA IL17R	Homo sapiens (human)	8	11
Q96F45	Zinc finger protein 503	ZNF503 NOLZ1	Homo sapiens (human)	1	1
Q96F25	UDP-N-acetylglucosamine transferase subunit ALG14	ALG14	Homo sapiens (human)	0	1	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94
Q96F24	Nuclear receptor-binding factor 2	NRBF2 COPR	Homo sapiens (human)	0	1
Q96F07	Cytoplasmic FMR1-interacting protein 2	CYFIP2 KIAA1168 PIR121	Homo sapiens (human)	2	1
Q96F05	Uncharacterized protein C11orf24	C11orf24	Homo sapiens (human)	16	7
Q96EZ8	Microspherule protein 1	MCRS1 INO80Q MSP58	Homo sapiens (human)	0	1
Q96EZ4	Myeloma-overexpressed gene protein	MYEOV OCIM	Homo sapiens (human)	1	1
Q96EY8	Corrinoid adenosyltransferase MMAB	MMAB	Homo sapiens (human)	2	1
Q96EY7	Small ribosomal subunit protein mS39	PTCD3 MRPS39	Homo sapiens (human)	2	1

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