GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **7651 - 7675** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
5284	polymeric immunoglobulin receptor	PIGR
5283	phosphatidylinositol glycan anchor biosynthesis class H	PIGH GPI-H phosphatidylinositol N-acetylglucosaminyltransferase subunit H	autistic disorder cancer embryoma epilepsy microcephaly 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
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
5276	serpin family I member 2	SERPINI2
5274	serpin family I member 1	SERPINI1
5270	serpin family E member 2	SERPINE2
5269	serpin family B member 6	SERPINB6
5268	serpin family B member 5	SERPINB5
5267	serpin family A member 4	SERPINA4
5265	serpin family A member 1	SERPINA1
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
5253	PHD finger protein 2	PHF2
5252	PHD finger protein 1	PHF1
5251	phosphate regulating endopeptidase X-linked	PHEX
5245	prohibitin 1	PHB1
5244	ATP binding cassette subfamily B member 4	ABCB4
5243	ATP binding cassette subfamily B member 1	ABCB1
5241	progesterone receptor	PGR
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

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