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 **16376 - 16400** 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
Q8NBF6	Late secretory pathway protein AVL9 homolog	AVL9 KIAA0241	Homo sapiens (human)	3	1
Q9HB55	Cytochrome P450 3A43	CYP3A43	Homo sapiens (human)	0	1
Q16514	Transcription initiation factor TFIID subunit 12	TAF12 TAF15 TAF2J TAFII20	Homo sapiens (human)	2	1
A0A5A4LJP0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P05187	Alkaline phosphatase, placental type	ALPP PLAP	Homo sapiens (human)	2	1	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 Becker muscular dystrophy Bloom syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Marfan syndrome Pick's disease Q fever Reye syndrome Sjogren's syndrome Waardenburg syndrome type 1 Waardenburg syndrome Wilson disease X-linked lymphoproliferative syndrome 2 absence epilepsy achondroplasia acromegaly acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult cystic teratoma adult hypophosphatasia adult lymphoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis ankylosing spondylitis autoimmune pancreatitis 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 azoospermia bladder carcinoma bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease cartilage disease central nervous system lymphoma cerebral degeneration cerebral palsy cervical adenocarcinoma cervical cancer cervix carcinoma childhood absence epilepsy childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation connective tissue disease craniosynostosis cystic teratoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis distal myopathy dysplastic nevus syndrome embryoma embryonal cancer endemic goiter endometriosis of uterus endometriosis endomyocardial fibrosis esophagitis essential thrombocythemia exanthem extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypocalciuric hypercalcemia 1 fragile X syndrome gallbladder disease gastroesophageal reflux disease gastrointestinal system cancer germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glaucoma glioblastoma goiter heart disease hematologic cancer hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypercalcemia hyperpituitarism hypogonadism hypophosphatasia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis infantile hypophosphatasia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intrahepatic cholangiocarcinoma iron metabolism disease islet cell tumor isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer leukemia limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma malignant pleural mesothelioma malignant teratoma mature teratoma melanoma multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nasopharynx carcinoma nephrocalcinosis nephrolithiasis neuroblastoma neurodegenerative disease non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter 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 obsolete constipation obsolete ymphosarcoma obstructive lung disease oculopharyngeal muscular dystrophy osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis periodontitis phosphorus metabolism disease placenta cancer pleomorphic lipoma primary biliary cholangitis primary hyperparathyroidism progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma rhabdomyosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy steatotic liver disease stomach cancer stomach carcinoma subcortical band heterotopia substernal goiter teratoma testicular cancer testicular germ cell cancer testis seminoma thyroid gland disease trypanosomiasis tuberculosis tuberous sclerosis type 2 diabetes mellitus typhus ulcerative colitis uremia uric acid nephrolithiasis urinary bladder cancer uveal melanoma vitelliform macular dystrophy well-differentiated liposarcoma
Q86WB7	Protein unc-93 homolog A	UNC93A	Homo sapiens (human)	1	0
A0A2K4XGP6	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q5T7F0	Neuropilin	NRP1	Homo sapiens (human)	2	0
Q8N1G4	Leucine-rich repeat-containing protein 47	LRRC47 KIAA1185	Homo sapiens (human)	2	1
P58417	Neurexophilin-1	NXPH1 NPH1	Homo sapiens (human)	6	1
Q15466	Nuclear receptor subfamily 0 group B member 2	NR0B2 SHP	Homo sapiens (human)	0	1
Q9UMQ6	Calpain-11	CAPN11	Homo sapiens (human)	0	1
P20042	Eukaryotic translation initiation factor 2 subunit 2	EIF2S2 EIF2B	Homo sapiens (human)	1	2
A6NMX2	Eukaryotic translation initiation factor 4E type 1B	EIF4E1B	Homo sapiens (human)	0	1
P22607	Fibroblast growth factor receptor 3	FGFR3 JTK4	Homo sapiens (human)	6	4
O00567	Nucleolar protein 56	NOP56 NOL5A	Homo sapiens (human)	5	5
Q8NH55	Olfactory receptor 52E5	OR52E5	Homo sapiens (human)	2	2
Q6J272	Ciliary microtubule inner protein 2A	CIMIP2A FAM166A	Homo sapiens (human)	0	1
O14647	Chromodomain-helicase-DNA-binding protein 2	CHD2	Homo sapiens (human)	2	1
Q8N135	Leucine-rich repeat LGI family member 4	LGI4 LGIL3	Homo sapiens (human)	2	2
Q9UL54	Serine/threonine-protein kinase TAO2	TAOK2 KIAA0881 MAP3K17 PSK PSK1	Homo sapiens (human)	1	1
Q5TF21	Microtubule cross-linking factor 3	MTCL3 C6orf174 SOGA3	Homo sapiens (human)	2	1
A0A0K0K1A5	T cell receptor beta variable 6-5	TRBV6-5	Homo sapiens (human)	1	0
A0A1W1B672	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
P51580	Thiopurine S-methyltransferase	TPMT	Homo sapiens (human)	0	1

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