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 **13926 - 13950** 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
P30711	Glutathione S-transferase theta-1	GSTT1	Homo sapiens (human)	0	1
P78417	Glutathione S-transferase omega-1	GSTO1 GSTTLP28	Homo sapiens (human)	1	1
P09211	Glutathione S-transferase P	GSTP1 FAEES3 GST3	Homo sapiens (human)	0	1
P21266	Glutathione S-transferase Mu 3	GSTM3 GST5	Homo sapiens (human)	0	1
P28161	Glutathione S-transferase Mu 2	GSTM2 GST4	Homo sapiens (human)	1	1
O43813	Glutathione S-transferase LANCL1	LANCL1 GPR69A	Homo sapiens (human)	2	2
P09210	Glutathione S-transferase A2	GSTA2 GST2	Homo sapiens (human)	0	1
O14880	Glutathione S-transferase 3, mitochondrial	MGST3	Homo sapiens (human)	0	1
Q86SX6	Glutaredoxin-related protein 5, mitochondrial	GLRX5 C14orf87	Homo sapiens (human)	0	1
O76003	Glutaredoxin-3	GLRX3 PICOT TXNL2	Homo sapiens (human)	0	1
P35754	Glutaredoxin-1	GLRX GRX	Homo sapiens (human)	1	2
O43716	Glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial	GATC 15E1.2	Homo sapiens (human)	0	1
Q07075	Glutamyl aminopeptidase	ENPEP	Homo sapiens (human)	21	145
C9JS14	Glutaminyl-peptide cyclotransferase (Fragment)	QPCT	Homo sapiens (human)	1	0
B5MCZ9	Glutaminyl-peptide cyclotransferase (Fragment)	QPCT	Homo sapiens (human)	1	0
Q16769	Glutaminyl-peptide cyclotransferase	QPCT	Homo sapiens (human)	5	12
Q6IA69	Glutamine-dependent NAD(+) synthetase	NADSYN1	Homo sapiens (human)	1	1
P47897	Glutamine--tRNA ligase	QARS1 QARS	Homo sapiens (human)	2	2
Q06210	Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1	GFPT1 GFAT GFPT	Homo sapiens (human)	1	2	Bell's palsy Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome achondroplasia agnosia brain cancer breast cancer breast carcinoma cancer centronuclear myopathy clubfoot congenital myasthenic syndrome 12 congenital myasthenic syndrome 4C congenital myasthenic syndrome congenital ptosis congenital structural myopathy developmental coordination disorder diabetes mellitus diabetic ketoacidosis embryoma facial nerve disease facial paralysis familial hyperlipidemia familial periodic paralysis giant cell glioblastoma glioblastoma glomerulonephritis hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertropia isolated elevated serum creatine phosphokinase levels kidney disease liver cancer mechanical strabismus myopathy nasopharynx carcinoma nephritis nephrosis neuromuscular disease neuromuscular junction disease obesity ophthalmoplegia pancreatic cancer pancreatic carcinoma ptosis pyoureter scoliosis stomach cancer stomach carcinoma strabismus tubular aggregate myopathy 1 type 2 diabetes mellitus
P15104	Glutamine synthetase	GLUL GLNS	Homo sapiens (human)	1	1	Addison's disease 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 Chagas disease Clostridium difficile colitis Graves' disease Griscelli syndrome type 2 Lafora disease Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Stiff-Person syndrome Wernicke-Korsakoff syndrome Wilson disease acquired immunodeficiency syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adrenal cortical hypofunction adrenoleukodystrophy adult oligodendroglioma alcohol dependence alcohol use disorder alcoholic liver cirrhosis alternating hemiplegia of childhood amino acid metabolic disorder amnestic disorder amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy bacterial sepsis basal ganglia disease bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer brain disease brain stem infarction breast cancer breast carcinoma cancer cannabis abuse cannabis dependence carbamoyl phosphate synthetase I deficiency disease carcinoma cardiovascular system disease central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood oligodendroglioma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome complex partial epilepsy congenital hypothyroidism coronary artery disease dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma exanthem follicular adenoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hemochromatosis hepatic coma hepatic encephalopathy hepatoblastoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperglycemia hyperthyroidism hypothyroidism immune system disease intrahepatic cholangiocarcinoma iron metabolism disease irritable bowel syndrome lingual-facial-buccal dyskinesia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression microcystic adenoma microphthalmia mixed glioma mixed oligodendroglioma-astrocytoma molybdenum cofactor deficiency type A mood disorder movement disease myelitis myopia myxedema nervous system disease neurocirculatory asthenia neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 oligodendroglioma ornithine carbamoyltransferase deficiency osteosarcoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma papillary adenoma placental insufficiency progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder purpura retinal disease retinitis retrograde amnesia sarcoma sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma steatotic liver disease stomach cancer stomach carcinoma temporal lobe epilepsy thyrotoxicosis trypanosomiasis tuberculosis 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 urea cycle disorder visual epilepsy
Q2KHR3	Glutamine and serine-rich protein 1	QSER1	Homo sapiens (human)	40	3
Q8NB37	Glutamine amidotransferase-like class 1 domain-containing protein 1	GATD1 FERRY5 PDDC1	Homo sapiens (human)	1	0
O94925	Glutaminase kidney isoform, mitochondrial	GLS GLS1 KIAA0838	Homo sapiens (human)	1	7
Q7L0X2	Glutamate-rich protein 6	ERICH6 C3orf44 FAM194A	Homo sapiens (human)	0	1
Q6P6B1	Glutamate-rich protein 5	ERICH5 C8orf47	Homo sapiens (human)	0	1

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