GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **6501 - 6525** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
53918	pelota mRNA surveillance and ribosome rescue factor	PELO
27043	proline, glutamate and leucine rich protein 1	PELP1
10400	phosphatidylethanolamine N-methyltransferase	PEMT PEMPT PEMT2	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 Chanarin-Dorfman syndrome Down syndrome Pick's disease Reye syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bladder carcinoma breast cancer breast carcinoma cancer capillary disease cerebral degeneration choline deficiency disease coronary artery disease diabetes mellitus diabetic ketoacidosis gallbladder disease hepatocellular carcinoma hereditary hemorrhagic telangiectasia homocystinuria liver cancer liver carcinoma liver cirrhosis liver disease obesity schizophrenia skin benign neoplasm skin cancer steatotic liver disease telangiectasis type 2 diabetes mellitus urinary bladder cancer
5187	period circadian regulator 1	PER1
8864	period circadian regulator 2	PER2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
8863	period circadian regulator 3	PER3
8799	peroxisomal biogenesis factor 11 beta	PEX11B
5195	peroxisomal biogenesis factor 14	PEX14
5824	peroxisomal biogenesis factor 19	PEX19
8504	peroxisomal biogenesis factor 3	PEX3
5198	phosphoribosylformylglycinamidine synthase	PFAS
5201	prefoldin subunit 1	PFDN1
5207	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1	PFKFB1	Zollinger-Ellison syndrome cancer hyperinsulinism stomach cancer
5208	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	PFKFB2	bone osteosarcoma breast cancer cancer childhood acute lymphocytic leukemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma high grade glioma melanoma osteosarcoma placental insufficiency skin melanoma stomach cancer type 2 diabetes mellitus
5209	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3	PFKFB3	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 Fanconi anemia complementation group A Fanconi anemia Pick's disease Reye syndrome actinic keratosis acute myeloid leukemia adenocarcinoma adenoma anaplastic astrocytoma arthritis arthropathy bacterial sepsis bipolar disorder bladder carcinoma bone marrow cancer bone osteosarcoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood osteosarcoma chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma depressive disorder dermatophytosis diabetes mellitus diabetic ketoacidosis embryoma esophagus squamous cell carcinoma essential hypertension extrinsic cardiomyopathy fibrillary astrocytoma fungal infectious disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hypertension hypoglycemia juvenile pilocytic astrocytoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder malignant astrocytoma malignant pleural mesothelioma melancholic depression melanoma mood disorder morbid obesity multiple myeloma myeloproliferative neoplasm nasopharynx carcinoma neuroblastoma neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteosarcoma pancreatic cancer pilocytic astrocytoma primary pulmonary hypertension prostate cancer prostate carcinoma protoplasmic astrocytoma psoriatic arthritis rheumatoid arthritis seborrheic keratosis skin disease skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma 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 urinary bladder cancer
5210	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4	PFKFB4	anaplastic astrocytoma bladder carcinoma breast cancer breast carcinoma cancer central nervous system cancer childhood cerebral astrocytoma embryoma fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma invasive ductal carcinoma juvenile pilocytic astrocytoma liver cancer lung benign neoplasm lung carcinoma lung small cell carcinoma malignant astrocytoma melanoma mixed glioma pancreatic cancer pancreatic carcinoma pilocytic astrocytoma prostate cancer prostate carcinoma protoplasmic astrocytoma skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma urinary bladder cancer
5211	phosphofructokinase, liver type	PFKL	Down syndrome Lafora disease Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis bipolar disorder coronary artery disease cystinuria dentatorubral-pallidoluysian atrophy disease of metabolism early myoclonic encephalopathy galactosemia 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 hepatocellular carcinoma liver cancer mood disorder obsolete major affective disorder 1 obsolete major affective disorder 2 progressive myoclonus epilepsy 1A progressive myoclonus epilepsy tetralogy of Fallot ventricular septal defect
5213	phosphofructokinase, muscle	PFKM PFK-1 PPP1R122 protein phosphatase 1, regulatory subunit 122	D-bifunctional protein deficiency adenocarcinoma adenoma anemia breast cancer breast carcinoma cancer carcinoma carnitine palmitoyltransferase I deficiency cholecystolithiasis choledocholithiasis cholelithiasis coronary artery disease cribriform carcinoma cystinuria diabetes mellitus disease of metabolism embryoma galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout granular cell carcinoma hemolytic anemia hepatocellular carcinoma high grade glioma hyperglycemia hyperuricemia liver cancer liver carcinoma macrocytic anemia pancreatic cancer pancreatic carcinoma pseudosarcomatous fibromatosis renal tubular acidosis sarcomatoid carcinoma schizophrenia tuberculosis tubular adenocarcinoma type 2 diabetes mellitus
5214	phosphofructokinase, platelet	PFKP PFK-C PFKF Phosphofructokinase, platelet type	adenocarcinoma adenoma breast cancer cancer cholangiocarcinoma cribriform carcinoma disease of metabolism embryoma glycogen storage disease granular cell carcinoma intrahepatic cholangiocarcinoma obesity pancreatic cancer pancreatic carcinoma renal tubular acidosis tubular adenocarcinoma
5216	profilin 1	PFN1
5223	phosphoglycerate mutase 1	PGAM1 PGAM-B Phosphoglycerate mutase A, nonmuscle form	Creutzfeldt-Jakob disease Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma anaplastic astrocytoma anemia arthritis arthropathy bipolar disorder bladder carcinoma bone osteosarcoma breast cancer breast carcinoma cancer carcinoma central nervous system cancer childhood cerebral astrocytoma childhood osteosarcoma colorectal cancer colorectal carcinoma cribriform carcinoma embryoma fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma juvenile pilocytic astrocytoma large intestine cancer leiomyoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia malaria malignant astrocytoma microphthalmia mixed glioma myofibroma obsolete Matthew-Wood syndrome oligospermia osteoarthritis osteosarcoma pancreatic ductal adenocarcinoma pilocytic astrocytoma prostate cancer prostate carcinoma protoplasmic astrocytoma sarcomatoid carcinoma squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer uterine fibroid
5224	phosphoglycerate mutase 2	PGAM2 PGAM-M	Cockayne syndrome Cornelia de Lange syndrome D-bifunctional protein deficiency Dubowitz syndrome Greig cephalopolysyndactyly syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome cancer carnitine palmitoyltransferase I deficiency chondrodysplasia-pseudohermaphroditism syndrome cystinuria disease of metabolism endometrial cancer endometrial carcinoma familial periodic paralysis galactosemia 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 isolated elevated serum creatine phosphokinase levels kidney failure microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myoglobinuria myopathy prostate cancer prostate carcinoma pseudosarcomatous fibromatosis uterine corpus cancer
441531	phosphoglycerate mutase family member 4	PGAM4 PGAM-B PGAM1 PGAM3 dJ1000K24.1	male infertility
80055	post-GPI attachment to proteins inositol deacylase 1	PGAP1 Bst1 FLJ12377 GPI inositol-deacylase SPG67	Burkitt lymphoma Laron syndrome achondroplasia agnosia autosomal recessive intellectual developmental disorder brain disease cerebral degeneration choreatic disease congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy factor XII deficiency focal epilepsy fundus dystrophy holoprosencephaly 1 holoprosencephaly intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia paroxysmal nocturnal hemoglobinuria partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
27315	post-GPI attachment to proteins 2	PGAP2 CWH43-N FGF receptor activating protein 1 FRAG1 cell wall biogenesis 43 N-terminal homolog (S. cerevisiae)	Beckwith-Wiedemann syndrome CLOVES syndrome Cogan syndrome Hirschsprung's disease Perlman syndrome Sotos syndrome Unverricht-Lundborg syndrome blepharospasm bone osteosarcoma cancer capillary disease childhood osteosarcoma cleft palate craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy embryoma esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 3 hyperphosphatemia intellectual disability isolated cleft palate learning disability monocular esotropia oligohydramnios osteosarcoma scoliosis sensorineural hearing loss syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy

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