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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 **7751 - 7775** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
5058	p21 (RAC1) activated kinase 1	PAK1	Homo sapiens (human)
5055	serpin family B member 2	SERPINB2	Homo sapiens (human)
5054	serpin family E member 1	SERPINE1	Homo sapiens (human)
5052	peroxiredoxin 1	PRDX1	Homo sapiens (human)
5051	platelet activating factor acetylhydrolase 2	PAFAH2 Aliases: HSD-PLA2	Homo sapiens (human)	coronary artery disease
5050	platelet activating factor acetylhydrolase 1b catalytic subunit 3	PAFAH1B3 Aliases: PAF-AH1b alpha 1 subunit	Homo sapiens (human)	intellectual disability learning disability
5049	platelet activating factor acetylhydrolase 1b catalytic subunit 2	PAFAH1B2 Aliases: PAF-AH1b alpha 2 subunit	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 Pick's disease Reye syndrome cancer cerebral degeneration embryoma lymphoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma
5048	platelet activating factor acetylhydrolase 1b regulatory subunit 1	PAFAH1B1 Aliases: LIS1 NudF PAFAH lissencephaly-1	Homo sapiens (human)	3p deletion syndrome Alzheimer's disease Angelman syndrome B-cell lymphoma Behcet's disease Crohn's colitis Crohn's disease Ewing sarcoma Gaucher's disease type I Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Joubert syndrome Langerhans-cell histiocytosis Marfan syndrome Miller-Dieker lissencephaly syndrome NFIA-related disorder Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease REM sleep behavior disorder Rett syndrome SATB2-associated syndrome Shwachman-Diamond syndrome Smith-Magenis syndrome West syndrome X-linked juvenile retinoschisis 1 Zellweger syndrome acute monocytic leukemia acute myeloid leukemia adult medulloblastoma adult respiratory distress syndrome aggressive periodontitis allergic asthma alternating hemiplegia of childhood anxiety disorder aplastic anemia asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer central nervous system disease childhood acute myeloid leukemia childhood leukemia childhood medulloblastoma childhood osteosarcoma chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17p13.1 deletion syndrome chromosome 17p13.3 duplication syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic monocytic leukemia chronic myelomonocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome dementia depressive disorder distal 10q deletion syndrome distal arthrogryposis dysthymic disorder dystonia embryoma epilepsy essential thrombocythemia essential tremor familial adenomatous polyposis 1 familial adenomatous polyposis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis hematologic cancer hepatocellular carcinoma high grade glioma hydranencephaly hydrocephalus impulse control disorder inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia kidney disease kleptomania late onset Parkinson's disease learning disability leukemia lingual-facial-buccal dyskinesia lissencephaly 1 lissencephaly liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephaly mood disorder movement disease multiple myeloma multiple system atrophy myelodysplastic syndrome myelodysplastic/myeloproliferative neoplasm myeloproliferative neoplasm nephritis nephrosis nervous system disease neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete constipation obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus oculocerebrorenal syndrome omphalocele osteosarcoma papillary renal cell carcinoma periodontosis periventricular nodular heterotopia peroxisome biogenesis disorder 1A phobic disorder polycystic ovary syndrome polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postural orthostatic tachycardia syndrome progressive supranuclear palsy psychotic disorder pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinitis pigmentosa 13 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder subcortical band heterotopia syndromic X-linked intellectual disability Najm type trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis ulcerative colitis umbilical hernia vascular disease visual epilepsy
5047	progestagen associated endometrial protein	PAEP	Homo sapiens (human)
5046	proprotein convertase subtilisin/kexin type 6	PCSK6	Homo sapiens (human)
5045	furin, paired basic amino acid cleaving enzyme	FURIN	Homo sapiens (human)
5042	poly(A) binding protein cytoplasmic 3	PABPC3	Homo sapiens (human)
5037	phosphatidylethanolamine binding protein 1	PEBP1	Homo sapiens (human)
5036	proliferation-associated 2G4	PA2G4	Homo sapiens (human)
5034	prolyl 4-hydroxylase subunit beta	P4HB	Homo sapiens (human)
5033	prolyl 4-hydroxylase subunit alpha 1	P4HA1	Homo sapiens (human)
5032	purinergic receptor P2Y11	P2RY11	Homo sapiens (human)
5031	pyrimidinergic receptor P2Y6	P2RY6	Homo sapiens (human)
5029	purinergic receptor P2Y2	P2RY2	Homo sapiens (human)
5028	purinergic receptor P2Y1	P2RY1	Homo sapiens (human)
5027	purinergic receptor P2X 7	P2RX7	Homo sapiens (human)
5026	purinergic receptor P2X 5	P2RX5	Homo sapiens (human)
5025	purinergic receptor P2X 4	P2RX4	Homo sapiens (human)
5024	purinergic receptor P2X 3	P2RX3	Homo sapiens (human)
5023	purinergic receptor P2X 1	P2RX1	Homo sapiens (human)

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