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 **3201 - 3225** of **18496** in total

« First

‹ Prev

…

125

126

127

128

129

130

131

132

133

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q2MV58	Tectonic-1	TCTN1 TECT1	Homo sapiens (human)	5	4
Q5HYD7	Phosphoinositide phospholipase C	DKFZp686K101	Homo sapiens (human)	2	0
Q9Y4J8	Dystrobrevin alpha	DTNA DRP3	Homo sapiens (human)	1	3
A0A141AZE3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P36543	V-type proton ATPase subunit E 1	ATP6V1E1 ATP6E ATP6E2	Homo sapiens (human)	1	1
O94875	Sorbin and SH3 domain-containing protein 2	SORBS2 ARGBP2 KIAA0777	Homo sapiens (human)	3	3
D4HP78	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8N0U4	Protein FAM185A	FAM185A	Homo sapiens (human)	0	1
Q9NTM9	Copper homeostasis protein cutC homolog	CUTC	Homo sapiens (human)	1	1
I1XV05	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q92990	Glomulin	GLMN FAP48 FAP68 VMGLOM	Homo sapiens (human)	2	1
C9JUV8	Butyrophilin subfamily 3 member A3 (Fragment)	BTN3A3	Homo sapiens (human)	1	0
P25089	N-formyl peptide receptor 3	FPR3 FPRH1 FPRL2	Homo sapiens (human)	2	0
Q5T8I3	EEIG family member 2	EEIG2 FAM102B	Homo sapiens (human)	0	1
Q9UBW8	COP9 signalosome complex subunit 7a	COPS7A CSN7A DERP10	Homo sapiens (human)	0	1
Q01543	Friend leukemia integration 1 transcription factor	FLI1	Homo sapiens (human)	14	2
A0A1B0GUW4	ceramidase (Fragment)	ASAH1	Homo sapiens (human)	2	0
H3BQ21	Signal regulatory protein beta 1 (Fragment)	SIRPB1	Homo sapiens (human)	2	0
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
Q8TDD2	Transcription factor Sp7	SP7 OSX	Homo sapiens (human)	0	1
Q6NSB4	HP protein	HP	Homo sapiens (human)	4	0
Q96ES7	SAGA-associated factor 29	SGF29 CCDC101	Homo sapiens (human)	1	1
A0A6B9HQY7	HLA class I histocompatibility antigen	HLA-B	Homo sapiens (human)	1	0
Q15059	Bromodomain-containing protein 3	BRD3 KIAA0043 RING3L	Homo sapiens (human)	6	1
P55317	Hepatocyte nuclear factor 3-alpha	FOXA1 HNF3A TCF3A	Homo sapiens (human)	8	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements