GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6576 - 6600** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
90102	pleckstrin homology like domain family B member 2	PHLDB2
23239	PH domain and leucine rich repeat protein phosphatase 1	PHLPP1
23035	PH domain and leucine rich repeat protein phosphatase 2	PHLPP2
162466	phosphoethanolamine/phosphocholine phosphatase 1	PHOSPHO1	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
57661	PHD and ring finger domains 1	PHRF1
10745	putative homeodomain transcription factor 1	PHTF1
57157	putative homeodomain transcription factor 2	PHTF2
9796	phytanoyl-CoA 2-hydroxylase interacting protein	PHYHIP
84457	phytanoyl-CoA 2-hydroxylase interacting protein like	PHYHIPL
51050	peptidase inhibitor 15	PI15
221476	peptidase inhibitor 16	PI16
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A DKFZP761G1923 PI4KII PIK42A	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
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
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
5298	phosphatidylinositol 4-kinase beta	PI4KB PI4K-BETA pi4K92	EAST syndrome autosomal dominant nonsyndromic deafness hepatitis C severe acute respiratory syndrome
196500	PILR alpha associated neural protein	PIANP
8554	protein inhibitor of activated STAT 1	PIAS1
9063	protein inhibitor of activated STAT 2	PIAS2
8301	phosphatidylinositol binding clathrin assembly protein	PICALM
55367	p53-induced death domain protein 1	PIDD1 DKFZp434D229 MGC16925
9780	piezo type mechanosensitive ion channel component 1 (Er blood group)	PIEZO1
63895	piezo type mechanosensitive ion channel component 2	PIEZO2
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
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
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

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