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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 **6651 - 6675** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
5308	paired like homeodomain 2	PITX2	Homo sapiens (human)
64219	praja ring finger ubiquitin ligase 1	PJA1	Homo sapiens (human)
5310	polycystin 1, transient receptor potential channel interacting	PKD1 Aliases: PBP Pc-1 TRPP1 polycystin 1 transient receptor potential cation channel, subfamily P, member 1	Homo sapiens (human)	Alzheimer's disease Caroli disease Creutzfeldt-Jakob disease Duchenne muscular dystrophy Guillain-Barre syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Moyamoya disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Streptococcus pneumonia Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute interstitial pneumonia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia anaplastic astrocytoma angiomyolipoma arteriosclerotic cardiovascular disease atherosclerosis autoimmune pancreatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease azoospermia bacterial sepsis bone disease bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer cardiomyopathy cartilage disease cavernous hemangioma central nervous system cancer childhood cerebral astrocytoma chorioangioma chronic kidney disease clear cell renal cell carcinoma collagen disease colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cutaneous fibrous histiocytoma cystic fibrosis cystic kidney disease dermoid cyst dextrocardia diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endomyocardial fibrosis epilepsy episodic kinesigenic dyskinesia 1 essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor growth hormone secreting pituitary adenoma hemangioma hemoglobin H disease hidradenoma high grade glioma histiocytoid hemangioma hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza insulinoma intracranial aneurysm intramuscular hemangioma isolated elevated serum creatine phosphokinase levels juvenile pilocytic astrocytoma keratosis follicularis kidney cancer kidney disease kidney failure large intestine cancer lipoid nephrosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioma lymphopenia malignant astrocytoma melanoma mesangial proliferative glomerulonephritis mixed glioma mongolian spot muscular dystrophy myocardial infarction nephritis nephrolithiasis nephrosis nephrotic syndrome neurofibromatosis 1 neurofibromatosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis non-congenital cyst of kidney nutmeg liver obesity osteosarcoma pancreatic cancer pancreatic carcinoma papilloma parapsoriasis pilocytic astrocytoma pneumonia polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease 4 polycystic kidney disease polycystic liver disease polycystic ovary syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter red color blindness renal carcinoma renal cell carcinoma renovascular hypertension rheumatoid arthritis silent myocardial infarction situs inversus skin melanoma skin papilloma skin tag squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma thalassemia thoracic aortic aneurysm thyroid gland anaplastic carcinoma tuberous sclerosis 1 tuberous sclerosis 2 tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis visual epilepsy
168507	polycystin 1 like 1, transient receptor potential channel interacting	PKD1L1	Homo sapiens (human)
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
342372	polycystin 1 like 3, transient receptor potential channel interacting	PKD1L3	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease cerebral infarction cerebrovascular disease episodic kinesigenic dyskinesia 1 prostate cancer prostate carcinoma
5311	polycystin 2, transient receptor potential cation channel	PKD2 Aliases: PC2 PKD4 Pc-2 TRPP2 transient receptor potential cation channel, subfamily P, member 2	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Wiskott-Aldrich syndrome acute kidney failure adrenal gland cancer atrial fibrillation atrioventricular block autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cholangiocarcinoma chronic kidney disease ciliopathy collagen disease congenital heart disease congestive heart failure connective tissue disease cystic kidney disease disorder of sexual development distal arthrogryposis duodenum cancer embryoma episodic kinesigenic dyskinesia 1 essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis focal segmental glomerulosclerosis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gout heart cancer hermaphroditism high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intracranial aneurysm intrahepatic cholangiocarcinoma islet cell tumor kidney disease kidney failure laryngeal squamous cell carcinoma lung adenocarcinoma lung cancer mixed glioma nephritis nephrosis neurodegenerative disease non-congenital cyst of kidney pheochromocytoma placental insufficiency polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 4 polycystic kidney disease polycystic liver disease prostate cancer prostate carcinoma pseudohermaphroditism pyoureter retinal degeneration situs inversus small intestine cancer thoracic aortic aneurysm tuberous sclerosis uremia urinary bladder cancer
9033	polycystin 2 like 1, transient receptor potential cation channel	PKD2L1	Homo sapiens (human)
27039	polycystin 2 like 2, transient receptor potential cation channel	PKD2L2	Homo sapiens (human)
91461	protein kinase domain containing, cytoplasmic	PKDCC	Homo sapiens (human)
10343	polycystin family receptor for egg jelly	PKDREJ	Homo sapiens (human)
5314	PKHD1 ciliary IPT domain containing fibrocystin/polyductin	PKHD1	Homo sapiens (human)
93035	PKHD1 like 1	PKHD1L1	Homo sapiens (human)
5313	pyruvate kinase L/R	PKLR	Homo sapiens (human)	Gaucher's disease acquired polycythemia anemia breast cancer breast carcinoma cancer cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism episodic kinesigenic dyskinesia 1 erythropoietin polycythemia familial erythrocytosis 1 familial erythrocytosis 2 favism gallbladder cancer gallbladder carcinoma hematopoietic system disease hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis hereditary sensory neuropathy type 4 hereditary sensory neuropathy hyperglycemia large intestine cancer liver cancer lung benign neoplasm macrocytic anemia major depressive disorder malaria melancholic depression metabolic dysfunction-associated steatotic liver disease obsolete melancholia optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma polycythemia vera polycythemia primary polycythemia prostate cancer prostate carcinoma pyruvate kinase deficiency of red cells sensory peripheral neuropathy stress polycythemia thalassemia type 2 diabetes mellitus
5315	pyruvate kinase M1/2	PKM Aliases: OIP3 PK3 THBP1	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 B-cell lymphoma Bloom syndrome Clostridium difficile colitis Cockayne syndrome Crohn's colitis Crohn's disease Gilles de la Tourette syndrome Klatskin's tumor Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Pick's disease Reye syndrome Van der Woude syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult medulloblastoma amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma childhood type dermatomyositis cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic cholangitis chronic fatigue syndrome chronic myeloid leukemia clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cystic fibrosis dermatomyositis disease of metabolism distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia enterocele esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance goiter granular cell carcinoma granulosa cell tumor head and neck cancer head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma hidradenoma high grade glioma hyperglycemia hyperhomocysteinemia hypertension ileitis ileocolitis immune system disease in situ carcinoma inflammatory bowel disease 1 inflammatory bowel disease influenza intrahepatic cholangiocarcinoma irritable bowel syndrome kidney cancer large intestine cancer leukemia liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microphthalmia mixed glioma multiple myeloma mycosis fungoides myelitis myeloproliferative disorder with eosinophilia myocardial infarction myositis nasopharynx carcinoma nephritis neurocirculatory asthenia nonpapillary renal cell carcinoma nontoxic goiter obesity obsolete Matthew-Wood syndrome obsolete hilar cholangiocellular carcinoma obsolete ymphosarcoma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma papillary transitional carcinoma placenta cancer prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma primary cutaneous amyloidosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis reflex sympathetic dystrophy renal carcinoma renal cell carcinoma renal infectious disease retrograde amnesia sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma syringoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer viral infectious disease
9088	protein kinase, membrane associated tyrosine/threonine 1	PKMYT1	Homo sapiens (human)
5585	protein kinase N1	PKN1	Homo sapiens (human)
5586	protein kinase N2	PKN2	Homo sapiens (human)
29941	protein kinase N3	PKN3	Homo sapiens (human)
5318	plakophilin 2	PKP2	Homo sapiens (human)
11187	plakophilin 3	PKP3	Homo sapiens (human)
8502	plakophilin 4	PKP4	Homo sapiens (human)
51365	phospholipase A1 member A	PLA1A Aliases: phosphatidylserine-specific phospholipase A1 ps-PLA1	Homo sapiens (human)
8399	phospholipase A2 group X	PLA2G10 Aliases: GXPLA2	Homo sapiens (human)	Crohn's colitis Crohn's disease Norum disease Tangier disease abdominal aortic aneurysm abetalipoproteinemia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma alternating hemiplegia of childhood anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma atherosclerosis autonomic neuropathy bacterial infectious disease bacterial sepsis bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease childhood cerebral astrocytoma cholangitis cholecystolithiasis choledocholithiasis cholelithiasis choreaacanthocytosis chronic kidney disease chronic obstructive pulmonary disease colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease craniosynostosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hypolipoproteinemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia malignant astrocytoma nervous system disease newborn respiratory distress syndrome nutmeg liver obsolete major affective disorder 1 obsolete major affective disorder 2 parapsoriasis pilocytic astrocytoma pleurisy primary sclerosing cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary coin lesion pustulosis of palm and sole rheumatoid arthritis schizophrenia sclerosing cholangitis subependymal giant cell astrocytoma suppurative cholangitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis visual epilepsy
81579	phospholipase A2 group XIIA	PLA2G12A	Homo sapiens (human)	Kuhnt-Junius degeneration age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder degeneration of macula and posterior pole macular degeneration schizophrenia

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