GlyCosmos Portal

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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	July 8, 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 **1051 - 1075** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
9060	3'-phosphoadenosine 5'-phosphosulfate synthase 2	PAPSS2 Aliases: ATPSK2 PAPS synthase 2 adenosine 5'-phosphosulfate kinase bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2	Homo sapiens (human)	Ehlers-Danlos syndrome Laron syndrome Marfan syndrome achondroplasia acne anovulation arthritis arthropathy brachyolmia diabetes mellitus diastrophic dysplasia hyperandrogenism hypertrichosis intellectual disability learning disability mucopolysaccharidosis IV multiple epiphyseal dysplasia osteoarthritis osteochondrodysplasia osteogenesis imperfecta polycystic ovary syndrome scoliosis situs inversus spondyloepimetaphyseal dysplasia, Pakistani type tuberous sclerosis type 2 diabetes mellitus
8505	poly(ADP-ribose) glycohydrolase	PARG	Homo sapiens (human)	acute myeloid leukemia autoimmune disease autoimmune lymphoproliferative syndrome bone osteosarcoma borna disease brain infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood leukemia childhood osteosarcoma colon carcinoma colorectal cancer embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma herpes simplex high grade glioma immune system disease leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma microphthalmia obsolete Matthew-Wood syndrome osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma stress-induced childhood-onset neurodegeneration with variable ataxia and seizures thyroid gland papillary carcinoma
142	poly(ADP-ribose) polymerase 1	PARP1 Aliases: ARTD1 PARP PARS Poly-PARP	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Barrett's esophagus Burkitt lymphoma Chagas disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Duchenne muscular dystrophy Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Gilles de la Tourette syndrome Graves' disease Hailey-Hailey disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Keshan disease Langerhans-cell histiocytosis Lynch syndrome MHC class II deficiency Marinesco-Sjogren syndrome Meniere's disease Nijmegen breakage syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Patau syndrome Peyronie's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Sertoli cell-only syndrome Sezary's disease Silver-Russell syndrome Stevens-Johnson syndrome T-cell acute lymphoblastic leukemia Treacher Collins syndrome Warsaw breakage syndrome Weissenbacher-Zweymuller syndrome Werner syndrome X-linked Aarskog syndrome X-linked ichthyosis Y-linked spermatogenic failure 1 Zika fever abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acrodermatitis acute biphenotypic leukemia acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosine deaminase deficiency adrenal gland cancer adrenoleukodystrophy adult fibrosarcoma adult medulloblastoma age related macular degeneration agranulocytosis alexia allergic asthma allergic rhinitis alopecia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia anemia anthrax disease anxiety disorder arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia with oculomotor apraxia type 1 atelosteogenesis atherosclerosis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial meningitis bacterial sepsis balanitis xerotica obliterans benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma bone marrow cancer bone osteosarcoma borna disease botryoid rhabdomyosarcoma brachydactyly type B1 brachydactyly brain cancer brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer childhood leukemia childhood medulloblastoma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chordoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic interstitial cystitis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital muscular dystrophy congestive heart failure corneal disease coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutis laxa deafness-dystonia-optic neuronopathy syndrome dedifferentiated liposarcoma degeneration of macula and posterior pole denture stomatitis depressive disorder dermatitis diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy differentiated thyroid gland carcinoma diffuse large B-cell lymphoma disease of metabolism dissociative amnesia distal arthrogryposis distal myopathy duodenum cancer dyslexia dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer embryonal rhabdomyosarcoma encephalitis encephalomyelitis endocrine exophthalmos endolymphatic hydrops endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus small cell carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia eye disease facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familiar ovarian carcinoma fibrillary astrocytoma fibrosarcoma follicular adenoma frozen shoulder gastroenteritis gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glycogen storage disease II goiter granular cell carcinoma granular corneal dystrophy 2 head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome hidradenoma high grade glioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypoparathyroidism-deafness-renal disease syndrome idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma intellectual disability intermediate coronary syndrome interstitial cystitis intestinal disease intracranial aneurysm intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconus kidney disease kidney failure large cell medulloblastoma large intestine cancer laryngeal squamous cell carcinoma learning disability leiomyoma leiomyosarcoma leukemia leukopenia limb-girdle muscular dystrophy liposarcoma liver cancer liver carcinoma liver cirrhosis luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphangioleiomyomatosis lymphoma macrocytic anemia macular degeneration major depressive disorder mal de Meleda malignant astrocytoma malignant mesothelioma malignant peripheral nerve sheath tumor malignant pleural mesothelioma mantle cell lymphoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction mitochondrial DNA depletion syndrome mixed glioma monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis muscular dystrophy myelitis myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myxoid leiomyosarcoma narcolepsy nasopharynx carcinoma nephritis nephroblastoma nephrosis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurofibrosarcoma neuronal ceroid lipofuscinosis 1 neurotic disorder neutropenia nodular nonsuppurative panniculitis non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete precursor B lymphoblastic lymphoma/leukemia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy oligospermia osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panniculitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis patent ductus arteriosus perinatal necrotizing enterocolitis peritoneal carcinoma pheochromocytoma phobic disorder phototoxic dermatitis pilocytic astrocytoma pleomorphic liposarcoma pneumonia premature menopause primary cerebellar degeneration primary cutaneous amyloidosis primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension proctitis progeria progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma prune belly syndrome psoriasis pulmonary emphysema pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory failure restrictive dermopathy reticulosarcoma retinal disease retinitis retrograde amnesia rhabdomyosarcoma rheumatic fever rheumatoid arthritis rippling muscle disease 2 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma secondary Parkinson disease senile cataract severe combined immunodeficiency severe congenital neutropenia silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag small intestine cancer spindle cell sarcoma sporadic breast cancer squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomatitis subependymal giant cell astrocytoma syringoma systemic lupus erythematosus systemic scleroderma teratocarcinoma thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia trigeminal neuralgia trypanosomiasis 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 ulcerative colitis ulcerative stomatitis uremia ureteral obstruction urinary bladder cancer uterine corpus cancer uterine fibroid uveal melanoma vasomotor rhinitis vertebrobasilar insufficiency viral infectious disease viral meningitis vitiligo xeroderma pigmentosum group A
84875	poly(ADP-ribose) polymerase family member 10	PARP10 Aliases: ARTD10 FLJ14464	Homo sapiens (human)	ataxia telangiectasia bipolar I disorder bipolar disorder hepatocellular carcinoma liver cancer neurodegenerative disease pancreatic cancer pancreatic carcinoma
57097	poly(ADP-ribose) polymerase family member 11	PARP11 Aliases: ARTD11	Homo sapiens (human)	microcephaly viral infectious disease
64761	poly(ADP-ribose) polymerase family member 12	PARP12 Aliases: ARTD12 FLJ22693 PARP-12 ZC3H1	Homo sapiens (human)	Zika fever age related macular degeneration cancer coronary artery disease degeneration of macula and posterior pole hepatocellular carcinoma influenza liver cancer macular degeneration viral infectious disease vitiligo
54625	poly(ADP-ribose) polymerase family member 14	PARP14 Aliases: ARTD8 BAL2 KIAA1268 pART8	Homo sapiens (human)	allergic asthma asthma cancer depressive disorder diffuse large B-cell lymphoma embryoma hepatocellular carcinoma intrinsic asthma liver cancer major depressive disorder melancholic depression multiple myeloma neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma
165631	poly(ADP-ribose) polymerase family member 15	PARP15 Aliases: ARTD7 BAL3 FLJ40597 pART7	Homo sapiens (human)	atherosclerosis cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
54956	poly(ADP-ribose) polymerase family member 16	PARP16 Aliases: ARTD15 FLJ20509 FLJ25281 pART15	Homo sapiens (human)
10038	poly(ADP-ribose) polymerase 2	PARP2 Aliases: ARTD2	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis azoospermia breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 coronary artery disease diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma hepatitis A hepatitis hepatocellular carcinoma lipoatrophic diabetes mellitus lipodystrophy liver cancer lymphopenia malignant peripheral nerve sheath tumor neurilemmoma neuroblastoma neurofibrosarcoma obesity peritoneal carcinoma prostate cancer prostate carcinoma rheumatoid arthritis steatotic liver disease type 2 diabetes mellitus
10039	poly(ADP-ribose) polymerase family member 3	PARP3 Aliases: ADPRT3 ARTD3 IRT1 NAD+ ADP-ribosyltransferase 3 hPARP-3 pADPRT-3 poly(ADP-ribose) polymerase 3 poly(ADP-ribose) synthetase-3	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease cystic fibrosis embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
143	poly(ADP-ribose) polymerase family member 4	PARP4 Aliases: ARTD4 VAULT3 VPARP VWA5C p193 vault poly(ADP-ribose) polymerase von Willebrand factor A domain containing 5C	Homo sapiens (human)	Down syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood leukemia colon cancer colonic benign neoplasm colorectal cancer embryoma esophagus squamous cell carcinoma goiter intracranial hypertension large intestine cancer leukemia lymphoma obsolete ymphosarcoma pancreatic cancer pancreatic carcinoma pseudotumor cerebri thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease
56965	poly(ADP-ribose) polymerase family member 6	PARP6 Aliases: ARTD17 pART17	Homo sapiens (human)	breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer
79668	poly(ADP-ribose) polymerase family member 8	PARP8 Aliases: ARTD16 FLJ21308 pART16	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
83666	poly(ADP-ribose) polymerase family member 9	PARP9 Aliases: ARTD9 BAL BAL1	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Gilles de la Tourette syndrome Goodpasture syndrome Loeffler syndrome Richter's syndrome Takayasu's arteritis X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agranulocytosis alcohol dependence alcohol use disorder allergic asthma anorexia nervosa asthma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bipolar disorder brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic granulomatous disease chronic lymphocytic leukemia chronic obstructive pulmonary disease complement deficiency cutaneous porphyria cystic fibrosis diffuse large B-cell lymphoma embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis farmer's lung gastric lymphoma giardiasis granulomatosis with polyangiitis hepatitis hepatocellular carcinoma heroin dependence hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza interstitial lung disease intrinsic asthma leukopenia liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 morphine dependence neutropenia newborn respiratory distress syndrome obesity obsolete ymphosarcoma opiate dependence pneumocystosis pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia prostate cancer prostate carcinoma pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis red-green color blindness rheumatoid arthritis sarcoidosis sarcoma schizophrenia scleroderma severe congenital neutropenia spindle cell sarcoma substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma tuberculosis tuberculous pneumothorax uveoparotid fever
5091	pyruvate carboxylase	PC Aliases: PCB	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 Burkitt lymphoma Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Pick's disease Reye syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adult fibrosarcoma alcohol dependence alcohol use disorder allergic asthma antiphospholipid syndrome antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant familial periodic fever bacterial sepsis beta thalassemia bipolar disorder blood coagulation disease breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma colitis congenital afibrinogenemia coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation embryoma enterobiasis epilepsy essential hypertension factor V deficiency factor VII deficiency familial hyperlipidemia fibrosarcoma gallbladder cancer gallbladder carcinoma gastroenteritis generalized anxiety disorder glomerulonephritis heart disease hemoglobin H disease hepatitis hepatocellular carcinoma holocarboxylase synthetase deficiency hyperglycemia hyperhomocysteinemia hyperlysinemia hypertension hyperthyroidism hyperuricemia hypoglycemia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease intellectual disability intestinal schistosomiasis intracranial sinus thrombosis ischemic colitis keratoconjunctivitis sicca kidney disease kwashiorkor lactic acidosis learning disability leukodystrophy liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphoma malignant exocrine pancreas neoplasm marasmus melanoma multiple sclerosis myocardial infarction nephritis nephrosis non-Hodgkin lymphoma nutrition disease obesity obsolete inherited blood coagulation disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma periventricular leukomalacia phobic disorder portal vein thrombosis protein C deficiency protein S deficiency protein-energy malnutrition purpura fulminans pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal tubular acidosis reticulosarcoma schistosomiasis silent myocardial infarction skin melanoma steatotic liver disease synovial sarcoma systemic lupus erythematosus thalassemia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis trichinosis tuberculosis type 2 diabetes mellitus urea cycle disorder visual epilepsy vitamin K deficiency bleeding
5095	propionyl-CoA carboxylase subunit alpha	PCCA	Homo sapiens (human)	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia nicotine dependence obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis refractive error severe congenital neutropenia sick sinus syndrome stomach cancer stomach carcinoma thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
5096	propionyl-CoA carboxylase subunit beta	PCCB	Homo sapiens (human)	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis amino acid metabolic disorder anemia anxiety disorder cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy generalized anxiety disorder granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis schizophrenia severe congenital neutropenia sick sinus syndrome thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
51294	protocadherin 12	PCDH12	Homo sapiens (human)
5105	phosphoenolpyruvate carboxykinase 1	PCK1 Aliases: PEPCK-C	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 abdominal obesity-metabolic syndrome 1 biliary atresia cancer celiac disease cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congestive heart failure cryptococcosis cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma epilepsy gestational diabetes hepatic coma hepatic encephalopathy hepatocellular carcinoma hyperglycemia hypoglycemia lactic acidosis large intestine cancer leprosy lipoatrophic diabetes mellitus lipodystrophy liver cancer liver carcinoma maturity-onset diabetes of the young metabolic dysfunction-associated steatohepatitis multiple sclerosis obesity optic atrophy placental insufficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency schizophrenia steatotic liver disease type 2 diabetes mellitus visual epilepsy
5106	phosphoenolpyruvate carboxykinase 2, mitochondrial	PCK2 Aliases: PEPCK PEPCK2	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma hepatitis C hepatocellular carcinoma hyperglycemia hypoglycemia kwashiorkor liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus melanoma nutrition disease obesity osteosarcoma prostate cancer prostate carcinoma protein-energy malnutrition pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer skin melanoma steatotic liver disease type 2 diabetes mellitus viral infectious disease
5111	proliferating cell nuclear antigen	PCNA	Homo sapiens (human)	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia
5130	phosphate cytidylyltransferase 1A, choline	PCYT1A Aliases: CCTalpha CT CTP:phosphocholine cytidylyltransferase-alpha CTPCT choline-phosphate cytidylyltransferase alpha phosphate cytidylyltransferase 1, choline, alpha isoform phosphorylcholine transferase alpha	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 Cockayne syndrome Down syndrome Graves' disease Laron syndrome Leber congenital amaurosis Pick's disease Prinzmetal angina Reye syndrome Richter's syndrome Turner syndrome X-linked dilated cardiomyopathy abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acquired color blindness acute chest syndrome acute myeloid leukemia acute myocardial infarction acute vascular insufficiency of intestine adult medulloblastoma alopecia anxiety disorder aortic aneurysm aortitis appendicitis arteriosclerotic cardiovascular disease arteriovenous malformation arteriovenous malformations of the brain astigmatism atherosclerosis atrial fibrillation 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 atrioventricular septal defect atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune thyroiditis blindness blue color blindness bone disease bone marrow cancer bone osteosarcoma brain cancer brain stem infarction bronchus cancer bronchus carcinoma cancer cardiac tamponade carotid artery thrombosis carotid stenosis cartilage disease cataract central sleep apnea cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia collagen disease colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness connective tissue disease corneal disease coronary artery anomaly coronary artery disease coronary stenosis coronary thrombosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy dissociated nystagmus embryoma embryonal cancer endocarditis epilepsy episodic kinesigenic dyskinesia 1 esophageal cancer esophageal carcinoma essential hypertension extramedullary plasmacytoma familial adenomatous polyposis fibromyalgia fundus dystrophy generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gonadal dysgenesis head and neck cancer hematologic cancer hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hyperthyroidism impotence infective endocarditis insulinoma intellectual disability intermittent claudication intracranial aneurysm intracranial thrombosis intrahepatic cholangiocarcinoma intussusception islet cell tumor keratoconus large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma multiple myeloma myeloid leukemia myelomeningocele myeloproliferative neoplasm myocardial infarction myopia neuroendocrine carcinoma neuroendocrine tumor night blindness nutmeg liver obsolete asthenopia osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma patent foramen ovale pathologic nystagmus peripheral artery disease peripheral vascular disease phobic disorder plasmacytoma polycythemia vera premature ejaculation primary pulmonary hypertension prostate cancer prostate carcinoma psychologic dyspareunia pterygium pulmonary embolism red color blindness red-green color blindness rheumatoid arthritis schizophrenia scoliosis seminoma sensorineural hearing loss sick sinus syndrome silent myocardial infarction skin melanoma spina bifida spinocerebellar ataxia type 8 split hand-foot malformation 1 spondyloepimetaphyseal dysplasia, Strudwick type spondylometaphyseal dysplasia with cone-rod dystrophy spontaneous ocular nystagmus squamous cell carcinoma squamous cell neoplasm subacute bacterial endocarditis superior mesenteric artery syndrome testicular cancer testis seminoma tethered spinal cord syndrome thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy
9468	phosphate cytidylyltransferase 1B, choline	PCYT1B Aliases: CCT-beta CCTbeta CTB CTP:phosphocholine cytidylyltransferase-beta choline-phosphate cytidylyltransferase beta phosphorylcholine transferase beta	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 Clouston syndrome Leber congenital amaurosis 1 Pick's disease Reye syndrome adult respiratory distress syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma breast ductal carcinoma cancer cerebral degeneration cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis large intestine cancer liver cancer liver carcinoma newborn respiratory distress syndrome progressive muscular atrophy prostate cancer prostate carcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis
5833	phosphate cytidylyltransferase 2, ethanolamine	PCYT2 Aliases: CTP:phosphoethanolamine cytidylyltransferase ET ethanolamine-phosphate cytidylyltransferase: phosphorylethanolamine transferase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cerebral degeneration embryoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 82 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia

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GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

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