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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 **6451 - 6475** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
27250	programmed cell death 4	PDCD4	Homo sapiens (human)
10015	programmed cell death 6 interacting protein	PDCD6IP	Homo sapiens (human)
10846	phosphodiesterase 10A	PDE10A Aliases: cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A	Homo sapiens (human)
50940	phosphodiesterase 11A	PDE11A Aliases: Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A	Homo sapiens (human)
5139	phosphodiesterase 3A	PDE3A Aliases: CGI-PDE cGMP-inhibited 3',5'-cyclic phosphodiesterase A	Homo sapiens (human)
5140	phosphodiesterase 3B	PDE3B Aliases: HcGIP1	Homo sapiens (human)
5142	phosphodiesterase 4B	PDE4B Aliases: cAMP-specific 3',5'-cyclic phosphodiesterase 4B phosphodiesterase E4 dunce homolog (Drosophila)	Homo sapiens (human)
9659	phosphodiesterase 4D interacting protein	PDE4DIP	Homo sapiens (human)
8654	phosphodiesterase 5A	PDE5A	Homo sapiens (human)
5158	phosphodiesterase 6B	PDE6B Aliases: CSNB3 CSNBAD2 RP40 congenital stationary night blindness 3, autosomal dominant rd1 rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta	Homo sapiens (human)
5154	platelet derived growth factor subunit A	PDGFA	Homo sapiens (human)
5155	platelet derived growth factor subunit B	PDGFB	Homo sapiens (human)
56034	platelet derived growth factor C	PDGFC	Homo sapiens (human)
80310	platelet derived growth factor D	PDGFD	Homo sapiens (human)
5156	platelet derived growth factor receptor alpha	PDGFRA	Homo sapiens (human)
5159	platelet derived growth factor receptor beta	PDGFRB	Homo sapiens (human)
5157	platelet derived growth factor receptor like	PDGFRL	Homo sapiens (human)
5160	pyruvate dehydrogenase E1 subunit alpha 1	PDHA1 Aliases: E1alpha pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial	Homo sapiens (human)	Coffin-Lowry syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease West syndrome abdominal obesity-metabolic syndrome 1 anemia arthritis arthropathy basal ganglia disease bile duct adenocarcinoma bile duct carcinoma blepharospasm cancer carcinoma cardiomyopathy cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy cholangiocarcinoma communicating hydrocephalus cone-rod dystrophy congenital nystagmus congenital ptosis coronary artery disease disease of metabolism dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy episodic ataxia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia fundus albipunctatus generalized dystonia head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma hydrocephalus hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder intellectual disability intrahepatic cholangiocarcinoma lactic acidosis learning disability leukodystrophy lingual-facial-buccal dyskinesia liver cancer macrocytic anemia mechanical strabismus microcephaly mitochondrial metabolism disease mitochondrial myopathy movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive hydrocephalus ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus peripheral nervous system disease placental insufficiency prostate cancer prostate carcinoma ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration retinitis pigmentosa sarcomatoid carcinoma senile degeneration of brain sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy
5161	pyruvate dehydrogenase E1 subunit alpha 2	PDHA2	Homo sapiens (human)	Marfan syndrome azoospermia disease of metabolism male infertility pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration situs inversus spermatogenic failure 1 spermatogenic failure tuberous sclerosis
5162	pyruvate dehydrogenase E1 subunit beta	PDHB Aliases: E1beta PDHE1B	Homo sapiens (human)	Leigh disease acute myocardial infarction breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis diabetes mellitus lactic acidosis luminal breast carcinoma A melanoma myocardial infarction nonpapillary renal cell carcinoma papillary adenocarcinoma papillary renal cell carcinoma pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma thyroid gland papillary carcinoma type 2 diabetes mellitus
8050	pyruvate dehydrogenase complex component X	PDHX Aliases: DLDBP E3BP OPDX PDX1 proX	Homo sapiens (human)	B-cell lymphoma Leigh disease MHC class II deficiency Zollinger-Ellison syndrome adenocarcinoma adenoma adenosine deaminase deficiency brain disease breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma craniosynostosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism dystonia embryoma endocrine pancreas disease epilepsy familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 granular cell carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism in situ carcinoma insulinoma intellectual disability kidney cancer lactic acidosis large intestine cancer learning disability locked-in syndrome maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young microcephaly microphthalmia neonatal diabetes obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma optic atrophy ovarian carcinoma ovarian mucinous neoplasm ovarian papillary neoplasm pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma paraplegia patent ductus arteriosus placental insufficiency polycystic kidney disease 1 primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency quadriplegia sarcoma severe combined immunodeficiency systemic lupus erythematosus transient neonatal diabetes mellitus tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus visual epilepsy
64714	protein disulfide isomerase family A member 2	PDIA2	Homo sapiens (human)
2923	protein disulfide isomerase family A member 3	PDIA3 Aliases: ERp57 ERp60 ERp61 GRP57 HsT17083 P58 PI-PLC	Homo sapiens (human)	Clostridium difficile colitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zika fever absence epilepsy acute myeloid leukemia adenocarcinoma adenoma allergic asthma amyotrophic lateral sclerosis arthritis arthropathy asphyxia neonatorum asthma autoimmune hepatitis breast cancer breast carcinoma breast ductal carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma depressive disorder dysplastic nevus syndrome embryoma endocrine system disease endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis epilepsy essential thrombocythemia giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma inflammatory and toxic neuropathy influenza intellectual disability intrinsic asthma invasive ductal carcinoma irritable bowel syndrome large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver cirrhosis lung cancer lung non-small cell carcinoma major depressive disorder male infertility melancholic depression melanoma mixed glioma mood disorder myelodysplastic syndrome neuroblastoma neurocirculatory asthenia neurodegenerative disease neurotic disorder nonpapillary renal cell carcinoma obsolete melancholia osteoarthritis ovarian cancer ovarian carcinoma papillary renal cell carcinoma platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 post-traumatic stress disorder primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma pulmonary hypertension renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spinocerebellar ataxia type 17 squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer visual epilepsy von Willebrand's disease
9601	protein disulfide isomerase family A member 4	PDIA4	Homo sapiens (human)
10954	protein disulfide isomerase family A member 5	PDIA5	Homo sapiens (human)

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