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 **2926 - 2950** 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
Q96FS4	Signal-induced proliferation-associated protein 1	SIPA1 SPA1	Homo sapiens (human)	0	1
O75182	Paired amphipathic helix protein Sin3b	SIN3B KIAA0700	Homo sapiens (human)	1	2
Q96ST3	Paired amphipathic helix protein Sin3a	SIN3A	Homo sapiens (human)	10	2
Q8NDZ2	SUMO-interacting motif-containing protein 1	SIMC1 C5orf25 PLEIAD	Homo sapiens (human)	1	1
Q14190	Single-minded homolog 2	SIM2 BHLHE15	Homo sapiens (human)	0	1
P81133	Single-minded homolog 1	SIM1 BHLHE14	Homo sapiens (human)	0	1
A0A0S2Z6B4	Nucleotide exchange factor SIL1 (Fragment)	SIL1	Homo sapiens (human)	1	0
Q9H173	Nucleotide exchange factor SIL1	SIL1	Homo sapiens (human)	16	12
D6REA1	Nucleotide exchange factor SIL1	SIL1	Homo sapiens (human)	1	0
Q9BRV8	Suppressor of IKBKE 1	SIKE1 SIKE	Homo sapiens (human)	0	1
Q9Y2K2	Serine/threonine-protein kinase SIK3	SIK3 KIAA0999 QSK	Homo sapiens (human)	1	1
Q9H0K1	Serine/threonine-protein kinase SIK2	SIK2 KIAA0781 QIK SNF1LK2	Homo sapiens (human)	0	1
P57059	Serine/threonine-protein kinase SIK1	SIK1 SIK SNF1LK	Homo sapiens (human)	0	1
Q8N7X8	SIGLEC family-like protein 1	SIGLECL1 C19orf75	Homo sapiens (human)	3	1
Q9Y336	Sialic acid-binding Ig-like lectin 9	SIGLEC9	Homo sapiens (human)	8	0	Guillain-Barre syndrome Miller Fisher syndrome allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis cancer carcinoma chikungunya chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma dengue hemorrhagic fever embryoma giant cell glioblastoma glioblastoma hepatitis high grade glioma intrinsic asthma large intestine cancer lung cancer lung non-small cell carcinoma melanoma pulmonary emphysema rheumatoid arthritis sarcomatoid carcinoma skin melanoma
Q9NYZ4	Sialic acid-binding Ig-like lectin 8	SIGLEC8 SAF2	Homo sapiens (human)	3	27	Hirschsprung's disease Loeffler syndrome allergic asthma anisakiasis asthma cancer chronic obstructive pulmonary disease colitis eosinophilic esophagitis eosinophilic gastritis eosinophilic gastroenteritis eosinophilic pneumonia gastritis gastroenteritis hypereosinophilic syndrome ileitis ileocolitis intrinsic asthma pneumonia pulmonary eosinophilia
Q9Y286	Sialic acid-binding Ig-like lectin 7	SIGLEC7 AIRM1	Homo sapiens (human)	8	32	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Guillain-Barre syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenosquamous carcinoma adult fibrosarcoma adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis alternating hemiplegia of childhood amyotrophic lateral sclerosis ankylosing spondylitis arthritis arthropathy atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autonomic neuropathy autosomal dominant familial periodic fever benign mesothelioma bipolar disorder bone marrow cancer brain stem infarction breast cancer breast carcinoma cancer cellular schwannoma central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood medulloblastoma chordoma chronic lymphocytic leukemia chronic monocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy delusional disorder depressive disorder dermatitis detrusor sphincter dyssynergia diabetes mellitus diabetic ketoacidosis dysthymic disorder eating disorder embryoma endometriosis of uterus endometriosis epilepsy esophagus squamous cell carcinoma familial combined hyperlipidemia familial hypercholesterolemia familial retinoblastoma fibrosarcoma gallbladder disease gangliocytoma ganglioneuroblastoma ganglioneuroma gastrinoma gastrointestinal system cancer gliosarcoma glomerulonephritis hepatitis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperglycemia hyperinsulinism kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver disease lymphoid leukemia major depressive disorder malignant mesothelioma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma melanotic neurilemmoma microphthalmia mixed glioma motor peripheral neuropathy myeloid leukemia myeloproliferative neoplasm nephritis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurotic disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia osteoarthritis pancreatic ductal adenocarcinoma panic disorder paranoid schizophrenia plexiform schwannoma preretinal fibrosis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma retinoblastoma rheumatoid arthritis rhinitis sick sinus syndrome situs inversus skin melanoma squamous cell carcinoma steatotic liver disease supratentorial primitive neuroectodermal tumor tendinitis tongue squamous cell carcinoma trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus vasomotor rhinitis
O43699	Sialic acid-binding Ig-like lectin 6	SIGLEC6 CD33L CD33L1 OBBP1	Homo sapiens (human)	5	2	Richter's syndrome chronic lymphocytic leukemia colorectal cancer colorectal carcinoma large intestine cancer subacute bacterial endocarditis systemic lupus erythematosus
O15389	Sialic acid-binding Ig-like lectin 5	SIGLEC5 CD33L2 OBBP2	Homo sapiens (human)	8	33	acute myeloid leukemia acute pericementitis aggressive periodontitis cancer diabetes mellitus diabetic ketoacidosis leprosy periodontitis periodontosis systemic lupus erythematosus type 2 diabetes mellitus
A6NMB1	Sialic acid-binding Ig-like lectin 16	SIGLEC16 SIGLECP16	Homo sapiens (human)	5	2
Q6ZMC9	Sialic acid-binding Ig-like lectin 15	SIGLEC15 CD33L3	Homo sapiens (human)	1	0	cancer embryoma osteoporosis
Q08ET2	Sialic acid-binding Ig-like lectin 14	SIGLEC14	Homo sapiens (human)	5	11
Q96PQ1	Sialic acid-binding Ig-like lectin 12	SIGLEC12 SIGLECL1 SLG	Homo sapiens (human)	11	1	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus
Q96RL6	Sialic acid-binding Ig-like lectin 11	SIGLEC11	Homo sapiens (human)	8	2
Q96LC7	Sialic acid-binding Ig-like lectin 10	SIGLEC10 SLG2	Homo sapiens (human)	6	4	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma

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