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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

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

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
90102	pleckstrin homology like domain family B member 2	PHLDB2	Homo sapiens (human)
23239	PH domain and leucine rich repeat protein phosphatase 1	PHLPP1	Homo sapiens (human)
23035	PH domain and leucine rich repeat protein phosphatase 2	PHLPP2	Homo sapiens (human)
162466	phosphoethanolamine/phosphocholine phosphatase 1	PHOSPHO1	Homo sapiens (human)	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
57661	PHD and ring finger domains 1	PHRF1	Homo sapiens (human)
10745	putative homeodomain transcription factor 1	PHTF1	Homo sapiens (human)
57157	putative homeodomain transcription factor 2	PHTF2	Homo sapiens (human)
9796	phytanoyl-CoA 2-hydroxylase interacting protein	PHYHIP	Homo sapiens (human)
84457	phytanoyl-CoA 2-hydroxylase interacting protein like	PHYHIPL	Homo sapiens (human)
51050	peptidase inhibitor 15	PI15	Homo sapiens (human)
221476	peptidase inhibitor 16	PI16	Homo sapiens (human)
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A Aliases: DKFZP761G1923 PI4KII PIK42A	Homo sapiens (human)	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B Aliases: FLJ11105 PI4KIIB PIK42B	Homo sapiens (human)	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 Aliases: PI4K-ALPHA phosphatidylinositol 4-kinase III alpha phosphatidylinositol 4-kinase IIIα pi4K230	Homo sapiens (human)	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 Aliases: PI4K-BETA pi4K92	Homo sapiens (human)	EAST syndrome autosomal dominant nonsyndromic deafness hepatitis C severe acute respiratory syndrome
196500	PILR alpha associated neural protein	PIANP	Homo sapiens (human)
8554	protein inhibitor of activated STAT 1	PIAS1	Homo sapiens (human)
9063	protein inhibitor of activated STAT 2	PIAS2	Homo sapiens (human)
8301	phosphatidylinositol binding clathrin assembly protein	PICALM	Homo sapiens (human)
55367	p53-induced death domain protein 1	PIDD1 Aliases: DKFZp434D229 MGC16925	Homo sapiens (human)
9780	piezo type mechanosensitive ion channel component 1 (Er blood group)	PIEZO1	Homo sapiens (human)
63895	piezo type mechanosensitive ion channel component 2	PIEZO2	Homo sapiens (human)
5277	phosphatidylinositol glycan anchor biosynthesis class A	PIGA Aliases: GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	Homo sapiens (human)	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 Aliases: GPI mannosyltransferase 3 GPI-MT-III PIG-B dol-P-Man dependent GPI mannosyltransferase III	Homo sapiens (human)	axonal neuropathy developmental and epileptic encephalopathy 80 epilepsy intellectual disability learning disability sleeping sickness visual epilepsy
5279	phosphatidylinositol glycan anchor biosynthesis class C	PIGC Aliases: GPI2 PIG-C phosphatidylinositol N-acetylglucosaminyltransferase subunit C	Homo sapiens (human)	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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