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 **2701 - 2725** 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
Q9ULF5	Zinc transporter ZIP10	SLC39A10 KIAA1265 ZIP10	Homo sapiens (human)	14	13
Q8NBW4	Neutral amino acid transporter 9	SLC38A9 URLC11	Homo sapiens (human)	4	0
Q8IZM9	Solute carrier family 38 member 6	SLC38A6 NAT1 SNAT6	Homo sapiens (human)	2	0
Q8WUX1	Sodium-coupled neutral amino acid transporter 5	SLC38A5 JM24 SN2 SNAT5	Homo sapiens (human)	1	0
Q969I6	Sodium-coupled neutral amino acid transporter 4	SLC38A4 ATA3 NAT3 SNAT4	Homo sapiens (human)	3	0
Q99624	Sodium-coupled neutral amino acid transporter 3	SLC38A3 G17 NAT1 SN1 SNAT3	Homo sapiens (human)	5	0
Q96QD8	Sodium-coupled neutral amino acid symporter 2	SLC38A2 ATA2 KIAA1382 SAT2 SNAT2	Homo sapiens (human)	2	1
Q08AI6	Putative sodium-coupled neutral amino acid transporter 11	SLC38A11 AVT2	Homo sapiens (human)	4	1
Q9HBR0	Solute carrier family 38 member 10	SLC38A10	Homo sapiens (human)	24	2
Q9H2H9	Sodium-coupled neutral amino acid symporter 1	SLC38A1 ATA1 NAT2 SAT1 SNAT1	Homo sapiens (human)	2	0
Q8NCC5	Sugar phosphate exchanger 3	SLC37A3 SPX3	Homo sapiens (human)	2	0
Q8TED4	Glucose-6-phosphate exchanger SLC37A2	SLC37A2	Homo sapiens (human)	3	0
P57057	Glucose-6-phosphate exchanger SLC37A1	SLC37A1 G3PP	Homo sapiens (human)	2	0
Q6YBV0	Neutral amino acid uniporter 4	SLC36A4 PAT4	Homo sapiens (human)	3	3
Q7Z2H8	Proton-coupled amino acid transporter 1	SLC36A1 PAT1	Homo sapiens (human)	3	0
Q8N357	Solute carrier family 35 member F6	SLC35F6 C2orf18	Homo sapiens (human)	1	1	microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma
Q96K37	Solute carrier family 35 member E1	SLC35E1	Homo sapiens (human)	0	1
Q9NQQ7	Solute carrier family 35 member C2	SLC35C2 C20orf5 OVCOV1	Homo sapiens (human)	1	0
Q9H1N7	Adenosine 3'-phospho 5'-phosphosulfate transporter 2	SLC35B3 C6orf196 PAPST2	Homo sapiens (human)	3	0	diabetes mellitus type 2 diabetes mellitus
Q8TB61	Adenosine 3'-phospho 5'-phosphosulfate transporter 1	SLC35B2 PAPST1	Homo sapiens (human)	0	1	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, mixed cellularity Langerhans cell sarcoma Langerhans-cell histiocytosis Richter's syndrome adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood lymphoma chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia dendritic cell sarcoma dilated cardiomyopathy 1A dilated cardiomyopathy follicular dendritic cell sarcoma follicular lymphoma hereditary multiple exostoses interdigitating dendritic cell sarcoma invasive ductal carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma non-Hodgkin lymphoma obesity obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma reticulosarcoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood
Q9BS91	UDP-sugar transporter protein SLC35A5	SLC35A5	Homo sapiens (human)	2	1
Q96G79	Probable UDP-sugar transporter protein SLC35A4	SLC35A4	Homo sapiens (human)	0	1	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
L0R6Q1	SLC35A4 upstream open reading frame protein	SLC35A4	Homo sapiens (human)	0	1
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	Homo sapiens (human)	0	1	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
P78382	CMP-sialic acid transporter	SLC35A1	Homo sapiens (human)	0	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis viral infectious disease visual epilepsy

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