GlyCosmos Portal

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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 **124401 - 124425** 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
P05622	Platelet-derived growth factor receptor beta	Pdgfrb Pdgfr Pdgfr1	Mus musculus (house mouse)	11	5
A0A5F8MPH8	Tenascin XB	Tnxb	Mus musculus (house mouse)	4	5
Q02563	Synaptic vesicle glycoprotein 2A	Sv2a Sv2	Rattus norvegicus (Norway rat)	3	5
P31327	Carbamoyl-phosphate synthase [ammonia], mitochondrial	CPS1	Homo sapiens (human)	7	5
Q9Y210	Short transient receptor potential channel 6	TRPC6 TRP6	Homo sapiens (human)	5	5
Q8TDW0	Volume-regulated anion channel subunit LRRC8C	LRRC8C AD158 FAD158	Homo sapiens (human)	6	5
P04007	Ribonuclease S-2	S-2	Nicotiana alata (Persian tobacco)	3	5
Q9UPN3	Microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5	MACF1 ABP620 ACF7 KIAA0465 KIAA0754 KIAA1251	Homo sapiens (human)	23	5
Q9NR96	Toll-like receptor 9	TLR9	Homo sapiens (human)	14	5
Q8C170	Unconventional myosin-IXa	Myo9a Myr7	Mus musculus (house mouse)	5	5
B0V2N1	Receptor-type tyrosine-protein phosphatase S	Ptprs	Mus musculus (house mouse)	4	5
Q99K86	Bcam protein	Bcam Lu	Mus musculus (house mouse)	3	5
Q02246	Contactin-2	CNTN2 AXT TAG1 TAX1	Homo sapiens (human)	13	5	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Gamstorp-Wohlfart syndrome Guillain-Barre syndrome Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Unverricht-Lundborg syndrome Van der Woude syndrome Wolff-Parkinson-White syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis adult T-cell leukemia/lymphoma adult lymphoma adult oligodendroglioma anaplastic astrocytoma arthritis arthropathy atrial fibrillation atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bladder carcinoma blepharospasm bone marrow disease bone osteosarcoma cancer central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood oligodendroglioma childhood osteosarcoma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy early myoclonic encephalopathy embryoma epilepsy episodic ataxia type 1 fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma immune system disease intellectual disability juvenile pilocytic astrocytoma keratoconjunctivitis sicca learning disability leukemia lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma microcephaly mixed glioma mixed oligodendroglioma-astrocytoma myotonic dystrophy type 2 neurodegenerative disease neurofibroma neurofibromatosis 1 neurofibromatosis neurogenic arthropathy obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma partial motor epilepsy peripheral nervous system neoplasm pilocytic astrocytoma primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma retinal vascular occlusion rheumatoid arthritis schizophrenia spinal cord disease subependymal giant cell astrocytoma syringomyelia systemic Epstein-Barr virus positive T-cell lymphoma of childhood tropical spastic paraparesis urinary bladder cancer visual epilepsy
Q9Y2L5	Trafficking protein particle complex subunit 8	TRAPPC8 KIAA1012	Homo sapiens (human)	1	5
Q7L0X0	TLR4 interactor with leucine rich repeats	TRIL KIAA0644	Homo sapiens (human)	9	5
Q7L1S5	Carbohydrate sulfotransferase 9	CHST9	Homo sapiens (human)	7	5	acute lymphoblastic leukemia acute myeloid leukemia breast cancer breast carcinoma cancer coronary artery disease depressive disorder essential thrombocythemia hematologic cancer idiopathic scoliosis lymphoblastic lymphoma major depressive disorder melancholic depression myelodysplastic syndrome obsolete melancholia schizophrenia
Q9UPQ9	Trinucleotide repeat-containing gene 6B protein	TNRC6B KIAA1093	Homo sapiens (human)	9	5
Q8TER0	Sushi, nidogen and EGF-like domain-containing protein 1	SNED1	Homo sapiens (human)	20	5
Q8IZY2	Phospholipid-transporting ATPase ABCA7	ABCA7	Homo sapiens (human)	9	5
Q8N3Y3	Xylosyl- and glucuronyltransferase LARGE2	LARGE2 GYLTL1B	Homo sapiens (human)	3	5	Duchenne muscular dystrophy acute myocardial infarction autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
P53621	Coatomer subunit alpha	COPA	Homo sapiens (human)	3	5
Q10472	Polypeptide N-acetylgalactosaminyltransferase 1	GALNT1	Homo sapiens (human)	4	5	colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure heart valve disease hepatocellular carcinoma large intestine cancer liver cancer ovarian cancer ovarian carcinoma pulmonary valve stenosis stomach cancer stomach carcinoma
Q8BQ86	Carbohydrate sulfotransferase 8	Chst8	Mus musculus (house mouse)	5	5
Q68BL8	Olfactomedin-like protein 2B	OLFML2B	Homo sapiens (human)	12	5
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	Homo sapiens (human)	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer

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