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 **326 - 350** of **126547** in total

« First

‹ Prev

…

10

11

12

13

14

15

16

17

18

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▼
P07738	Bisphosphoglycerate mutase	BPGM	Homo sapiens (human)	6	0	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 normocytic anemia polycythemia vera polycythemia stress polycythemia
P00387	NADH-cytochrome b5 reductase 3	CYB5R3 DIA1	Homo sapiens (human)	3	2	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
Q6UXF7	C-type lectin domain family 18 member B	CLEC18B MRLP1	Homo sapiens (human)	1	0	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
Q13445	Transmembrane emp24 domain-containing protein 1	TMED1 IL1RL1L IL1RL1LG	Homo sapiens (human)	0	1	acquired immunodeficiency syndrome breast cancer human immunodeficiency virus infectious disease
Q6UXN8	C-type lectin domain family 9 member A	CLEC9A	Homo sapiens (human)	2	0	acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease herpes simplex human immunodeficiency virus infectious disease influenza leprosy pneumonia primary immunodeficiency disease tuberculosis viral infectious disease
Q7Z3E1	Protein mono-ADP-ribosyltransferase TIPARP	TIPARP PARP7	Homo sapiens (human)	1	1	acoustic neuroma alcohol dependence alcohol use disorder angiomatous meningioma benign meningioma cancer cerebral convexity meningioma cervical cancer cervix carcinoma clear cell meningioma embryoma fibrous meningioma hepatitis A hepatitis intraorbital meningioma intraventricular meningioma meningioma meningothelial meningioma microcystic meningioma olfactory groove meningioma ovarian cancer parasagittal meningioma pituitary adenoma psammomatous meningioma secretory meningioma spinal meningioma transitional meningioma
Q13421	Mesothelin	MSLN MPF	Homo sapiens (human)	4	31	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
Q7Z3S7	Voltage-dependent calcium channel subunit alpha-2/delta-4	CACNA2D4	Homo sapiens (human)	3	1	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness spontaneous ocular nystagmus strabismus
P42126	Enoyl-CoA delta isomerase 1, mitochondrial	ECI1 DCI	Homo sapiens (human)	0	1	achalasia carcinoma congenital diaphragmatic hernia dilated cardiomyopathy 1A dilated cardiomyopathy esophagitis gastroesophageal reflux disease hiatus hernia megaesophagus peptic esophagitis
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	Homo sapiens (human)	11	6	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
Q08AH1	Acyl-coenzyme A synthetase ACSM1, mitochondrial	ACSM1 BUCS1 LAE MACS1	Homo sapiens (human)	0	1	abdominal obesity-metabolic syndrome 1 carcinoma cerebral palsy depressive disorder essential hypertension hemiplegia hypertension idiopathic scoliosis lung benign neoplasm lung carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia sarcomatoid carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
Q8N0V5	N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase	GCNT2 GCNT5 II NACGT1	Homo sapiens (human)	2	2	abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma esophagus squamous cell carcinoma gallbladder cancer gallbladder carcinoma hyperferritinemia-cataract syndrome kidney failure large intestine cancer melanoma skin melanoma tuberculosis uremia
Q16822	Phosphoenolpyruvate carboxykinase [GTP], mitochondrial	PCK2 PEPCK2	Homo sapiens (human)	1	1	abdominal obesity-metabolic syndrome 1 bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma hepatitis C hepatocellular carcinoma hyperglycemia hypoglycemia kwashiorkor liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus melanoma nutrition disease obesity osteosarcoma prostate cancer prostate carcinoma protein-energy malnutrition pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer skin melanoma steatotic liver disease type 2 diabetes mellitus viral infectious disease
Q5KU26	Collectin-12	COLEC12 CLP1 NSR2 SCARA4 SRCL	Homo sapiens (human)	8	10	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
Q96N66	Lysophospholipid acyltransferase 7	MBOAT7 BB1 LENG4 OACT7	Homo sapiens (human)	1	1	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
P33121	Long-chain-fatty-acid--CoA ligase 1	ACSL1 FACL1 FACL2 LACS LACS1 LACS2	Homo sapiens (human)	4	2	abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bacterial sepsis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cervix uteri carcinoma in situ chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy endomyocardial fibrosis gliosarcoma glomerulonephritis glucose metabolism disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease kidney disease large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma mixed glioma myocardial infarction nephritis nephrosis nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 papillary renal cell carcinoma pyoureter renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction steatotic liver disease 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 vascular disease
P22732	Solute carrier family 2, facilitated glucose transporter member 5	SLC2A5 GLUT5	Homo sapiens (human)	1	0	abdominal obesity-metabolic syndrome 1 acute myeloid leukemia breast cancer breast carcinoma cancer central nervous system cancer childhood B-cell acute lymphoblastic leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus disease of metabolism embryoma essential hypertension gliosarcoma hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intestinal atresia large intestine cancer liver cancer long QT syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity ovarian cancer ovarian carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma tropical sprue type 2 diabetes mellitus
O95980	Reversion-inducing cysteine-rich protein with Kazal motifs	RECK ST15	Homo sapiens (human)	6	2	abdominal aortic aneurysm acute interstitial pneumonia adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adult respiratory distress syndrome ameloblastoma anaplastic astrocytoma arthritis arthropathy atrial fibrillation bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease childhood cerebral astrocytoma childhood osteosarcoma cholangiocarcinoma chorioamnionitis chronic obstructive pulmonary disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency cribriform carcinoma cutaneous fibrous histiocytoma cystic fibrosis distal arthrogryposis dysplastic nevus syndrome embryoma epilepsy epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma fibrosarcoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatitis C hepatocellular carcinoma hidradenoma high grade glioma idiopathic interstitial pneumonia intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma large intestine cancer leiomyoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma mixed glioma multiple myeloma myofibroma nasopharyngitis nasopharynx carcinoma necrotizing fasciitis nephroblastoma neurilemmoma neuroblastoma neurofibrosarcoma nodular prostate osteoarthritis osteosarcoma pancreatic cancer pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma patent ductus arteriosus periodontal disease periodontitis pilocytic astrocytoma prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoidosis sarcomatoid carcinoma skin melanoma skin papilloma skin tag squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma urinary bladder cancer uterine fibroid uveoparotid fever viral infectious disease
P16118	6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 1	PFKFB1 F6PK PFRX	Homo sapiens (human)	2	1	Zollinger-Ellison syndrome cancer hyperinsulinism stomach cancer
O43837	Isocitrate dehydrogenase [NAD] subunit beta, mitochondrial	IDH3B	Homo sapiens (human)	0	1	Zollinger-Ellison syndrome bipolar disorder blindness cataract cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus fundus dystrophy glaucoma hidradenitis suppurativa hidradenitis hyperinsulinism hypogonadism intellectual disability keratoconus learning disability obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus pompholyx retinitis pigmentosa 46 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma type 2 diabetes mellitus
P50213	Isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial	IDH3A	Homo sapiens (human)	1	1	Zollinger-Ellison syndrome alternating hemiplegia of childhood arthritis arthropathy autonomic neuropathy bipolar disorder blindness brain disease cancer cataract central nervous system disease cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus learning disability lung adenocarcinoma lung cancer nervous system disease obesity obsolete asthenopia ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus primary open angle glaucoma retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
Q68CP4	Heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT TMEM76	Homo sapiens (human)	5	19	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
Q8IWL1	Pulmonary surfactant-associated protein A2	SFTPA2 COLEC5 PSAP SFTP1 SFTPA SFTPA2B	Homo sapiens (human)	1	0	Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial sepsis bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cystic fibrosis embryoma esophagitis gastroesophageal reflux disease granular cell carcinoma heart disease hydrocephalus hypereosinophilic syndrome hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease interstitial nephritis intrinsic asthma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis newborn respiratory distress syndrome obstructive hydrocephalus obstructive lung disease otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory failure respiratory syncytial virus infectious disease rheumatoid arthritis secondary hypertrophic osteoarthropathy senile degeneration of brain spondyloarthropathy spondylosis squamous cell carcinoma tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis
Q9NQR9	Glucose-6-phosphatase 2	G6PC2 IGRP	Homo sapiens (human)	1	0	Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cystinuria diabetes mellitus diabetic ketoacidosis galactosemia gestational diabetes glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hyperglycemia hyperinsulinism insulinoma obsolete type 1 diabetes mellitus 9 prediabetes syndrome 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
Q99424	Peroxisomal acyl-coenzyme A oxidase 2	ACOX2	Homo sapiens (human)	1	1	Zellweger syndrome breast cancer breast carcinoma cardiovascular system disease congenital bile acid synthesis defect 6 heart disease hepatoblastoma hepatocellular carcinoma liver cancer obsolete steatorrhea peroxisome biogenesis disorder 1A

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements