GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **451 - 475** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
84720	phosphatidylinositol glycan anchor biosynthesis class O	PIGO DKFZp434M222 FLJ00135 PIG-O	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome absence epilepsy blepharospasm capillary disease childhood absence epilepsy cleft palate colorectal cancer colorectal carcinoma craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 2 imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability monocular esotropia nonepidermolytic palmoplantar keratoderma oligohydramnios palmoplantar keratosis scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
23556	phosphatidylinositol glycan anchor biosynthesis class N	PIGN GPI ethanolamine phosphate transferase 1 MCD4 PIG-N	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
93183	phosphatidylinositol glycan anchor biosynthesis class M	PIGM DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	Budd-Chiari syndrome epilepsy focal epilepsy paroxysmal nocturnal hemoglobinuria partial motor epilepsy portal hypertension portal vein thrombosis thrombophilia visual epilepsy
9487	phosphatidylinositol glycan anchor biosynthesis class L	PIGL N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase N-acetylglucosaminylphosphatidylinositol deacetylase PIG-L	CAKUT2 CHIME syndrome Cogan syndrome Hailey-Hailey disease Hirschsprung's disease Rothmund-Thomson syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome acquired hyperkeratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia amyotrophic lateral sclerosis anodontia autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB blepharospasm capillary disease cerebral degeneration chronic ulcer of skin cleft palate coloboma congenital ptosis craniosynostosis cutis laxa dextro-looped transposition of the great arteries diffuse interstitial keratitis disease of mental health early myoclonic encephalopathy epilepsy esotropia focal hand dystonia granuloma annulare hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hypertropia hypotrichosis ichthyosis intellectual disability isolated cleft palate learning disability lymphoblastic lymphoma mal de Meleda mechanical strabismus monocular esotropia multiple types of congenital heart defects 6 nonepidermolytic palmoplantar keratoderma obsolete dextro-looped transposition of the great arteries 1 oligohydramnios ophthalmoplegia palmoplantar keratosis progressive muscular atrophy psychotic disorder ptosis recurrent corneal erosion restrictive dermopathy scoliosis sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 telangiectasis tetralogy of Fallot tooth agenesis ventricular septal defect visual epilepsy
10026	phosphatidylinositol glycan anchor biosynthesis class K	PIGK GPI transamidase subunit GPI-anchor transamidase GPI8 GPI8 homolog (S. cerevisiae) PIG-K hGPI8	adult lymphoma cancer central nervous system lymphoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lymphoma obsolete ymphosarcoma
5283	phosphatidylinositol glycan anchor biosynthesis class H	PIGH GPI-H phosphatidylinositol N-acetylglucosaminyltransferase subunit H	autistic disorder cancer embryoma epilepsy microcephaly visual epilepsy
54872	phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group)	PIGG FLJ20265 GPI ethanolamine phosphate transferase 2 GPI7 LAS21 LAS21 (GPI7) homolog (S. cerevisiae)	cerebral degeneration epilepsy intellectual disability learning disability placental insufficiency visual epilepsy
5281	phosphatidylinositol glycan anchor biosynthesis class F	PIGF PIG-F	arteriosclerotic cardiovascular disease atherosclerosis bone osteosarcoma cancer cavernous hemangioma chorioangioma colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease embryonal cancer familial retinoblastoma germ cell and embryonal cancer germ cell cancer germinoma glomus tumor hemangioma histiocytoid hemangioma intramuscular hemangioma large intestine cancer lymphangioma osteosarcoma paroxysmal nocturnal hemoglobinuria placental insufficiency retinoblastoma systemic lupus erythematosus trilateral retinoblastoma
5279	phosphatidylinositol glycan anchor biosynthesis class C	PIGC GPI2 PIG-C phosphatidylinositol N-acetylglucosaminyltransferase subunit C	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease agnosia cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy glycosylphosphatidylinositol biosynthesis defect 16 intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nicotine dependence obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
9488	phosphatidylinositol glycan anchor biosynthesis class B	PIGB GPI mannosyltransferase 3 GPI-MT-III PIG-B dol-P-Man dependent GPI mannosyltransferase III	axonal neuropathy developmental and epileptic encephalopathy 80 epilepsy intellectual disability learning disability sleeping sickness visual epilepsy
5277	phosphatidylinositol glycan anchor biosynthesis class A	PIGA GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	Barrett's esophagus Burkitt lymphoma Hirschsprung's disease Marfan syndrome Miller-Dieker lissencephaly syndrome Simpson-Golabi-Behmel syndrome type 1 Simpson-Golabi-Behmel syndrome type 2 Unverricht-Lundborg syndrome West syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency aplastic anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atypical hemolytic-uremic syndrome autoimmune disease autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B blepharospasm blood coagulation disease bone marrow cancer brain disease cancer chondroma chromosome 17p13.1 deletion syndrome coronary thrombosis dental caries dentin caries developmental and epileptic encephalopathy 3 early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy esophagitis esophagus adenocarcinoma essential thrombocythemia extramedullary plasmacytoma fetal erythroblastosis focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth hematopoietic system disease hemoglobinuria hemolytic anemia hemolytic-uremic syndrome immune system disease inflammatory bowel disease intellectual disability learning disability lissencephaly multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction obsolete congenital ichthyosiform erythroderma obsolete infantile epileptic encephalopathy paroxysmal nocturnal hemoglobinuria patent foramen ovale peptic esophagitis plasma cell neoplasm plasmacytoma polycythemia vera primary pulmonary hypertension protein C deficiency protein S deficiency pulmonary embolism sensorineural hearing loss silent myocardial infarction situs inversus thrombophilia thrombotic thrombocytopenic purpura transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis vertebrobasilar insufficiency visual epilepsy
5298	phosphatidylinositol 4-kinase beta	PI4KB PI4K-BETA pi4K92	EAST syndrome autosomal dominant nonsyndromic deafness hepatitis C severe acute respiratory syndrome
5297	phosphatidylinositol 4-kinase alpha	PI4KA PI4K-ALPHA phosphatidylinositol 4-kinase III alpha phosphatidylinositol 4-kinase IIIα pi4K230	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 CEDNIK syndrome Pick's disease Reye syndrome anemia cancer cerebral degeneration chromosome 22q11.2 deletion syndrome, distal clubfoot disease of mental health hepatitis C hepatocellular carcinoma hereditary spastic paraplegia 84 hypomyelinating leukodystrophy 2 liver cancer macrocytic anemia prostate cancer prostate carcinoma psychotic disorder schizophrenia
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B FLJ11105 PI4KIIB PIK42B	attention deficit hyperactivity disorder bipolar disorder childhood leukemia chronic myeloid leukemia disease of mental health leukemia psychotic disorder schizophrenia
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A DKFZP761G1923 PI4KII PIK42A	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
162466	phosphoethanolamine/phosphocholine phosphatase 1	PHOSPHO1	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
5261	phosphorylase kinase catalytic subunit gamma 2	PHKG2	glycogen storage disease IXc glycogen storage disease liver cirrhosis
5260	phosphorylase kinase catalytic subunit gamma 1	PHKG1
5257	phosphorylase kinase regulatory subunit beta	PHKB	glycogen storage disease IXb
5256	phosphorylase kinase regulatory subunit alpha 2	PHKA2	glycogen storage disease IXa glycogen storage disease visceral heterotaxy
5255	phosphorylase kinase regulatory subunit alpha 1	PHKA1	glycogen storage disease IXd glycogen storage disease hypothyroidism
9489	phosphatidylglycerophosphate synthase 1	PGS1 DKFZP762M186	acute myeloid leukemia
283871	phosphoglycolate phosphatase	PGP	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 Ewing sarcoma Hirschsprung's disease Krukenberg carcinoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma allergic asthma alternating hemiplegia of childhood asthma autonomic neuropathy autosomal dominant polycystic kidney disease basal cell carcinoma bipolar disorder bone marrow disease brain ischemia breast cancer breast carcinoma cancer carcinoma central nervous system disease central nervous system lymphoma cerebral degeneration childhood leukemia chorioamnionitis chronic myeloid leukemia colon adenocarcinoma colorectal cancer colorectal carcinoma cribriform carcinoma degenerative disc disease depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder embryoma erythromelalgia essential hypertension essential thrombocythemia familial retinoblastoma glucose intolerance granular cell carcinoma hepatocellular carcinoma hypertension inflammatory bowel disease intrinsic asthma kidney cancer large intestine cancer leukemia lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung carcinoma lymphoid leukemia lymphoma major depressive disorder melancholic depression myelodysplastic syndrome myeloid leukemia myotonic dystrophy type 1 myotonic dystrophy type 2 nervous system disease neuroblastoma neurodegenerative disease neuroectodermal tumor neuropathy neurotic disorder obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma peripheral nervous system disease polycystic kidney disease 1 polyneuropathy prediabetes syndrome retinoblastoma rhabdomyosarcoma rhinitis schizophrenia sebaceous carcinoma sexual dysfunction squamous cell carcinoma sweat gland cancer tongue squamous cell carcinoma trilateral retinoblastoma 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 varicose veins vitiligo
5239	phosphoglucomutase 5	PGM5 PGMRP phosphoglucomutase-related protein	bladder carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma urinary bladder cancer
5238	phosphoglucomutase 3	PGM3 AGM1 DKFZP434B187 PAGM acetylglucosamine phosphomutase phosphoacetylglucosamine mutase	Desbuquois dysplasia Laron syndrome MHC class II deficiency Richter's syndrome achondroplasia adenosine deaminase deficiency agranulocytosis allergic asthma allergic rhinitis asthma atopic dermatitis bacterial sepsis breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma cervical cancer chronic ethmoiditis chronic lymphocytic leukemia chronic sphenoidal sinusitis chronic ulcer of skin combined T cell and B cell immunodeficiency congenital disorder of glycosylation cystic fibrosis dermatitis epilepsy esophagitis gastroesophageal reflux disease granuloma annulare hemolytic anemia hyper IgE recurrent infection syndrome 1 hypereosinophilic syndrome immunodeficiency 23 intellectual disability intrinsic asthma lactose intolerance learning disability lymphoma lymphopenia membranoproliferative glomerulonephritis mucopolysaccharidosis IV multiple epiphyseal dysplasia neuropathy neutropenia obsolete ymphosarcoma osteochondrodysplasia osteomyelitis otitis media pancytopenia peptic esophagitis peripheral nervous system disease polyneuropathy primary immunodeficiency disease scoliosis sensorineural hearing loss severe combined immunodeficiency severe congenital neutropenia subacute sclerosing panencephalitis teratoma vasomotor rhinitis visual epilepsy

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