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

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
5284	polymeric immunoglobulin receptor	PIGR	Homo sapiens (human)
5283	phosphatidylinositol glycan anchor biosynthesis class H	PIGH Aliases: GPI-H phosphatidylinositol N-acetylglucosaminyltransferase subunit H	Homo sapiens (human)	autistic disorder cancer embryoma epilepsy microcephaly visual epilepsy
5281	phosphatidylinositol glycan anchor biosynthesis class F	PIGF Aliases: PIG-F	Homo sapiens (human)	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 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
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
5276	serpin family I member 2	SERPINI2	Homo sapiens (human)
5274	serpin family I member 1	SERPINI1	Homo sapiens (human)
5270	serpin family E member 2	SERPINE2	Homo sapiens (human)
5269	serpin family B member 6	SERPINB6	Homo sapiens (human)
5268	serpin family B member 5	SERPINB5	Homo sapiens (human)
5267	serpin family A member 4	SERPINA4	Homo sapiens (human)
5265	serpin family A member 1	SERPINA1	Homo sapiens (human)
5261	phosphorylase kinase catalytic subunit gamma 2	PHKG2	Homo sapiens (human)	glycogen storage disease IXc glycogen storage disease liver cirrhosis
5260	phosphorylase kinase catalytic subunit gamma 1	PHKG1	Homo sapiens (human)
5257	phosphorylase kinase regulatory subunit beta	PHKB	Homo sapiens (human)	glycogen storage disease IXb
5256	phosphorylase kinase regulatory subunit alpha 2	PHKA2	Homo sapiens (human)	glycogen storage disease IXa glycogen storage disease visceral heterotaxy
5255	phosphorylase kinase regulatory subunit alpha 1	PHKA1	Homo sapiens (human)	glycogen storage disease IXd glycogen storage disease hypothyroidism
5253	PHD finger protein 2	PHF2	Homo sapiens (human)
5252	PHD finger protein 1	PHF1	Homo sapiens (human)
5251	phosphate regulating endopeptidase X-linked	PHEX	Homo sapiens (human)
5245	prohibitin 1	PHB1	Homo sapiens (human)
5244	ATP binding cassette subfamily B member 4	ABCB4	Homo sapiens (human)
5243	ATP binding cassette subfamily B member 1	ABCB1	Homo sapiens (human)
5241	progesterone receptor	PGR	Homo sapiens (human)
5239	phosphoglucomutase 5	PGM5 Aliases: PGMRP phosphoglucomutase-related protein	Homo sapiens (human)	bladder carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma urinary bladder cancer

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