GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7926 - 7950** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
5024	purinergic receptor P2X 3	P2RX3
5025	purinergic receptor P2X 4	P2RX4
5026	purinergic receptor P2X 5	P2RX5
9127	purinergic receptor P2X 6	P2RX6
5027	purinergic receptor P2X 7	P2RX7
5028	purinergic receptor P2Y1	P2RY1
5032	purinergic receptor P2Y11	P2RY11
64805	purinergic receptor P2Y12	P2RY12
53829	purinergic receptor P2Y13	P2RY13
9934	purinergic receptor P2Y14	P2RY14
5029	purinergic receptor P2Y2	P2RY2
10745	putative homeodomain transcription factor 1	PHTF1
57157	putative homeodomain transcription factor 2	PHTF2
90780	pygopus family PHD finger 2	PYGO2
84795	pyridine nucleotide-disulphide oxidoreductase domain 2	PYROXD2
23042	pyridoxal dependent decarboxylase domain containing 1	PDXDC1
5031	pyrimidinergic receptor P2Y6	P2RY6
149628	pyrin and HIN domain family member 1	PYHIN1
84109	pyroglutamylated RFamide peptide receptor	QRFPR
5831	pyrroline-5-carboxylate reductase 1	PYCR1
29920	pyrroline-5-carboxylate reductase 2	PYCR2
5091	pyruvate carboxylase	PC PCB	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 B-cell lymphoma Burkitt lymphoma Graves' disease 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 Langerhans-cell histiocytosis Pick's disease Reye syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adult fibrosarcoma alcohol dependence alcohol use disorder allergic asthma antiphospholipid syndrome antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant familial periodic fever bacterial sepsis beta thalassemia bipolar disorder blood coagulation disease breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma colitis congenital afibrinogenemia coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation embryoma enterobiasis epilepsy essential hypertension factor V deficiency factor VII deficiency familial hyperlipidemia fibrosarcoma gallbladder cancer gallbladder carcinoma gastroenteritis generalized anxiety disorder glomerulonephritis heart disease hemoglobin H disease hepatitis hepatocellular carcinoma holocarboxylase synthetase deficiency hyperglycemia hyperhomocysteinemia hyperlysinemia hypertension hyperthyroidism hyperuricemia hypoglycemia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease intellectual disability intestinal schistosomiasis intracranial sinus thrombosis ischemic colitis keratoconjunctivitis sicca kidney disease kwashiorkor lactic acidosis learning disability leukodystrophy liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphoma malignant exocrine pancreas neoplasm marasmus melanoma multiple sclerosis myocardial infarction nephritis nephrosis non-Hodgkin lymphoma nutrition disease obesity obsolete inherited blood coagulation disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma periventricular leukomalacia phobic disorder portal vein thrombosis protein C deficiency protein S deficiency protein-energy malnutrition purpura fulminans pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal tubular acidosis reticulosarcoma schistosomiasis silent myocardial infarction skin melanoma steatotic liver disease synovial sarcoma systemic lupus erythematosus thalassemia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis trichinosis tuberculosis type 2 diabetes mellitus urea cycle disorder visual epilepsy vitamin K deficiency bleeding
5160	pyruvate dehydrogenase E1 subunit alpha 1	PDHA1 E1alpha pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial	Coffin-Lowry syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease West syndrome abdominal obesity-metabolic syndrome 1 anemia arthritis arthropathy basal ganglia disease bile duct adenocarcinoma bile duct carcinoma blepharospasm cancer carcinoma cardiomyopathy cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy cholangiocarcinoma communicating hydrocephalus cone-rod dystrophy congenital nystagmus congenital ptosis coronary artery disease disease of metabolism dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy episodic ataxia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia fundus albipunctatus generalized dystonia head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma hydrocephalus hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder intellectual disability intrahepatic cholangiocarcinoma lactic acidosis learning disability leukodystrophy lingual-facial-buccal dyskinesia liver cancer macrocytic anemia mechanical strabismus microcephaly mitochondrial metabolism disease mitochondrial myopathy movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive hydrocephalus ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus peripheral nervous system disease placental insufficiency prostate cancer prostate carcinoma ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration retinitis pigmentosa sarcomatoid carcinoma senile degeneration of brain sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy
5161	pyruvate dehydrogenase E1 subunit alpha 2	PDHA2	Marfan syndrome azoospermia disease of metabolism male infertility pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration situs inversus spermatogenic failure 1 spermatogenic failure tuberous sclerosis
5162	pyruvate dehydrogenase E1 subunit beta	PDHB E1beta PDHE1B	Leigh disease acute myocardial infarction breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis diabetes mellitus lactic acidosis luminal breast carcinoma A melanoma myocardial infarction nonpapillary renal cell carcinoma papillary adenocarcinoma papillary renal cell carcinoma pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma thyroid gland papillary carcinoma type 2 diabetes mellitus

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