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 **122201 - 122225** 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
Q9UJ37	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	ST6GALNAC2 SIAT7B SIATL1 STHM	Homo sapiens (human)	4	2	IgA glomerulonephritis breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma depressive disorder embryoma large intestine cancer major depressive disorder melancholic depression melanoma obsolete melancholia skin melanoma thyroid gland follicular carcinoma
Q92184	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	ST6GALNAC2 SIAT7B	Gallus gallus (chicken)	2	0
Q92183	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	ST6GALNAC1 SIAT7A	Gallus gallus (chicken)	8	0
Q9NSC7	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	ST6GALNAC1 SIAT7A	Homo sapiens (human)	11	2	acute myocardial infarction bladder carcinoma breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer myocardial infarction ovarian cancer ovarian carcinoma schizophrenia silent myocardial infarction stomach cancer stomach carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
Q9QZ39	Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	St6galnac1 Siat7a	Mus musculus (house mouse)	5	1
P17050	Alpha-N-acetylgalactosaminidase	NAGA	Homo sapiens (human)	5	95	Clouston syndrome Fabry disease Kanzaki disease Schindler disease type 1 Unverricht-Lundborg syndrome acquired hyperkeratosis alternating hemiplegia of childhood autistic disorder autonomic neuropathy blepharospasm cancer cardiomyopathy cataract central nervous system disease central nervous system origin vertigo cerebral degeneration chylomicron retention disease congenital nystagmus dissociated nystagmus early myoclonic encephalopathy elephantiasis embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia gallbladder disease hypertrophic cardiomyopathy hypertropia influenza intellectual disability learning disability lipid storage disease liver disease lymphedema mechanical strabismus nervous system disease neuroaxonal dystrophy neurodegeneration with brain iron accumulation 2a neuropathy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 trichomoniasis visual epilepsy
Q9QWR8	Alpha-N-acetylgalactosaminidase	Naga	Mus musculus (house mouse)	3	4
Q66H12	Alpha-N-acetylgalactosaminidase	Naga	Rattus norvegicus (Norway rat)	4	0
Q90744	Alpha-N-acetylgalactosaminidase	NAGA	Gallus gallus (chicken)	3	0
Q58DH9	Alpha-N-acetylgalactosaminidase	NAGA	Bos taurus (cattle)	5	0
Q9H4F1	Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase	ST6GALNAC4 SIAT3C SIAT7D	Homo sapiens (human)	5	3	Guillain-Barre syndrome Miller Fisher syndrome cancer thyroid gland follicular carcinoma
Q9R2B6	Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase	St6galnac4 Siat7d	Mus musculus (house mouse)	1	0
K2MLW4	Alpha-MPP	MOQ_009654	Trypanosoma cruzi marinkellei	0	1
B9PUJ6	Alpha-MPP	BN1205_046660	Toxoplasma gondii VEG	0	1
A2QG68	Alpha-L-rhamnosidase rgxB	rgxB	Aspergillus niger CBS 513.88	14	0
P48441	Alpha-L-iduronidase	Idua	Mus musculus (house mouse)	7	8
Q3U1Z0	Alpha-L-iduronidase	Idua	Mus musculus (house mouse)	3	0
P35475	Alpha-L-iduronidase	IDUA	Homo sapiens (human)	6	10	Alzheimer's disease Balo concentric sclerosis Creutzfeldt-Jakob disease Fabry disease Gaucher's disease Hartnup disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Feil syndrome Krabbe disease Laron syndrome Loeys-Dietz syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Richter's syndrome Scheie syndrome Sly syndrome T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome achondroplasia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adrenoleukodystrophy adult medulloblastoma agranulocytosis anemia anogenital venereal wart aortic valve disease 2 aortic valve insufficiency aortic valve stenosis autosomal recessive hypophosphatemic rickets benign mesothelioma blindness bone disease brain cancer breast cancer breast carcinoma cancer cardiomyopathy cartilage disease central nervous system disease cerebral palsy childhood medulloblastoma chromophobe renal cell carcinoma chronic lymphocytic leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital heart disease connective tissue disease deficiency anemia dental caries dentin caries depressive disorder disease of mental health disease of metabolism dysthymic disorder embryoma endomyocardial fibrosis essential hypertension giant cell glioblastoma gingival hypertrophy gingival overgrowth glaucoma glioblastoma glycogen storage disease II glycoproteinosis head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma high grade glioma hydrocephalus hypertension hypertrophic cardiomyopathy hypochromic anemia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia inherited metabolic disorder intellectual disability intracranial hypotension large intestine cancer learning disability leukopenia lipid storage disease liver cancer liver carcinoma lung benign neoplasm lung carcinoma lymphoblastic lymphoma lysosomal storage disease macrocytic anemia major depressive disorder malignant mesothelioma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma microcytic anemia mitral valve insufficiency mitral valve prolapse mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih/s mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma narcolepsy nervous system disease neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteoporosis otitis media pancreatic ductal adenocarcinoma papillary renal cell carcinoma primary pulmonary hypertension psychotic disorder recurrent corneal erosion renal carcinoma renal cell carcinoma retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain sensorineural hearing loss severe congenital neutropenia skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spinal cord disease spondylolisthesis stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tracheal stenosis tyrosinemia type I tyrosinemia ulcerative colitis
Q01634	Alpha-L-iduronidase	IDUA	Canis lupus familiaris (dog)	6	0
Q3TDU4	Alpha-L-iduronidase	Idua	Mus musculus (house mouse)	3	0
Q9VKJ8	Alpha-L-iduronidase	Idua	Drosophila melanogaster (fruit fly)	7	0
Q9FXE5	Alpha-L-fucosidase 3	FXG1	Arabidopsis thaliana (thale cress)	4	0
Q8L7W8	Alpha-L-fucosidase 2	FUC95A AXY8	Arabidopsis thaliana (thale cress)	4	0
Q8GW72	Alpha-L-fucosidase 1	FUC1	Arabidopsis thaliana (thale cress)	6	0
C3YWU0	Alpha-L-fucosidase	BRAFLDRAFT_56888	Branchiostoma floridae (Florida lancelet)	4	0

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