GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H1I8	Activating signal cointegrator 1 complex subunit 2	ASCC2 ASC1P100 RQT3	0	1
Q8N9N2	Activating signal cointegrator 1 complex subunit 1	ASCC1	0	1
Q9H765	Ankyrin repeat and SOCS box protein 8	ASB8	0	1
Q8WXJ9	Ankyrin repeat and SOCS box protein 17	ASB17	0	1
Q8WXK1	Ankyrin repeat and SOCS box protein 15	ASB15	1	1
Q8WXI3	Ankyrin repeat and SOCS box protein 10	ASB10	0	1
Q9ULH1	Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1	ASAP1 DDEF1 KIAA1249 PAG2	1	1
Q9NR71	Neutral ceramidase	ASAH2 HNAC1	23	0	Alzheimer's disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome celiac disease colorectal cancer congenital diaphragmatic hernia cystic fibrosis dementia diabetes mellitus diabetic ketoacidosis gallbladder disease gamma heavy chain disease glaucoma heavy chain disease inflammatory bowel disease large intestine cancer liver disease lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neuroblastoma obesity systemic Epstein-Barr virus positive T-cell lymphoma of childhood type 2 diabetes mellitus
A0A1B0GUW4	ceramidase (Fragment)	ASAH1	2	0
A0A1B0GUA4	Acid ceramidase	ASAH1	2	0
A0A1B0GUG1	Acid ceramidase	ASAH1	2	0
A0A1B0GTP7	ceramidase	ASAH1	2	0
A0A1B0GUB3	ceramidase (Fragment)	ASAH1	2	0
A0A1B0GVG2	Acid ceramidase	ASAH1	2	0
A0A1B0GW68	Acid ceramidase	ASAH1	2	0
A0A1B0GTZ5	Acid ceramidase	ASAH1	2	0
A0A1B0GV06	ceramidase (Fragment)	ASAH1	2	0
A0A1B0GUE3	ceramidase	ASAH1	2	0
A0A1B0GUH5	Acid ceramidase	ASAH1	2	0
A0A1B0GTM3	Acid ceramidase	ASAH1	2	0
E7EMM4	Acid ceramidase	ASAH1	2	0
Q13510	Acid ceramidase	ASAH1 ASAH	8	123	Albright's hereditary osteodystrophy 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 Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
Q9HBK9	Arsenite methyltransferase	AS3MT CYT19	1	1
Q96QS3	Homeobox protein ARX	ARX	2	1
Q5T4W7	Artemin	ARTN EVN	3	1

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