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 **2201 - 2225** 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
Q8BGY3	Leucine zipper protein 2	Luzp2	Mus musculus (house mouse)	2	4
Q6NSW3	A-kinase anchor protein SPHKAP	Sphkap Kiaa1678	Mus musculus (house mouse)	7	4
A2AN08	E3 ubiquitin-protein ligase UBR4	Ubr4 Kiaa0462 Zubr1	Mus musculus (house mouse)	4	4
Q6ZMI0	Protein phosphatase 1 regulatory subunit 21	PPP1R21 CCDC128 FERRY2 KLRAQ1	Homo sapiens (human)	1	4
Q3UDW8	Heparan-alpha-glucosaminide N-acetyltransferase	Hgsnat D8Ertd354e Tmem76	Mus musculus (house mouse)	3	4
O15354	Prosaposin receptor GPR37	GPR37	Homo sapiens (human)	4	4
O35161	Cadherin EGF LAG seven-pass G-type receptor 1	Celsr1	Mus musculus (house mouse)	28	4
P01570	Interferon alpha-14	IFNA14	Homo sapiens (human)	1	4
O89017	Legumain	Lgmn Prsc1	Mus musculus (house mouse)	5	4
E9Q8H9	Complement component factor h	Cfh	Mus musculus (house mouse)	6	4
Q8NCH0	Carbohydrate sulfotransferase 14	CHST14 D4ST1	Homo sapiens (human)	6	4	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia arthropathy atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
Q80X19	Collagen alpha-1(XIV) chain	Col14a1	Mus musculus (house mouse)	5	4
Q96BA8	Cyclic AMP-responsive element-binding protein 3-like protein 1	CREB3L1 OASIS	Homo sapiens (human)	4	4
Q66HD0	Endoplasmin	Hsp90b1 Grp94 Hspc4 Tra1	Rattus norvegicus (Norway rat)	6	4
Q99LR1	Lysophosphatidylserine lipase ABHD12	Abhd12	Mus musculus (house mouse)	1	4
Q8K385	Ferric-chelate reductase 1	FRRS1 Sdfr2 Sdr2	Mus musculus (house mouse)	6	4
Q9HCU0	Endosialin	CD248 CD164L1 TEM1	Homo sapiens (human)	34	4	Ewing sarcoma anaplastic astrocytoma arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bone osteosarcoma brain cancer cancer carcinoma childhood cerebral astrocytoma childhood osteosarcoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease diarrhea disease of metabolism embryoma epithelioid sarcoma fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease influenza juvenile pilocytic astrocytoma large intestine cancer liver cancer liver cirrhosis lung small cell carcinoma malignant astrocytoma melanoma meningitis neuroblastoma obesity osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pilocytic astrocytoma pneumonia protoplasmic astrocytoma psoriatic arthritis rheumatoid arthritis sarcoma sarcomatoid carcinoma scleroderma shigellosis skin benign neoplasm skin cancer skin melanoma spindle cell sarcoma squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic scleroderma thrombotic thrombocytopenic purpura tongue squamous cell carcinoma urinary tract obstruction
Q0P6H9	Transmembrane protein 62	TMEM62	Homo sapiens (human)	6	4
P18075	Bone morphogenetic protein 7	BMP7 OP1	Homo sapiens (human)	5	4
Q01484	Ankyrin-2	ANK2 ANKB	Homo sapiens (human)	7	4
Q8K394	Inactive phospholipase C-like protein 2	Plcl2 Kiaa1092 Plce2	Mus musculus (house mouse)	3	4
Q60930	Voltage-dependent anion-selective channel protein 2	Vdac2 Vdac6	Mus musculus (house mouse)	3	4
Q13530	Serine incorporator 3	SERINC3 DIFF33 TDE1	Homo sapiens (human)	5	4
O60656	UDP-glucuronosyltransferase 1A9	UGT1A9 GNT1 UGT1	Homo sapiens (human)	3	4	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Plasmodium falciparum malaria abdominal obesity-metabolic syndrome 1 acute kidney failure adult hepatocellular carcinoma agranulocytosis atopic dermatitis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer cancer carcinoma childhood hepatocellular carcinoma cholecystolithiasis choledocholithiasis cholelithiasis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis dermatitis diabetes mellitus diarrhea embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D hepatocellular carcinoma influenza kidney disease large intestine cancer leukopenia liver cancer liver disease lung cancer lung non-small cell carcinoma neonatal jaundice neutropenia obesity obsolete constipation obsolete dyspepsia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma stomach cancer thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
Q86YL7	Podoplanin	PDPN GP36	Homo sapiens (human)	26	4

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