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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 **393051 - 393075** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
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
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
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
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
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
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
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
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
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
5067	contactin 3	CNTN3 Aliases: BIG-1	Homo sapiens (human)	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
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
5019	3-oxoacid CoA-transferase 1	OXCT1 Aliases: SCOT Succinyl-CoA:3-ketoacid-CoA transferase	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency cancer carbohydrate metabolic disorder central nervous system cancer coronary artery disease diabetes mellitus embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer localized scleroderma mixed glioma nutmeg liver obesity osteoporosis phenylketonuria reflex sympathetic dystrophy scleroderma sickle cell anemia systemic scleroderma type 2 diabetes mellitus
5016	oviductal glycoprotein 1	OVGP1 Aliases: CHIT5 oviductin	Homo sapiens (human)	bagassosis cancer centronuclear myopathy ciliary body disease colorectal cancer colorectal carcinoma congenital structural myopathy embryoma endometrial carcinoma endosalpingiosis iris disease large intestine cancer laryngitis ovarian cancer ovarian carcinoma panuveitis transient myeloproliferative syndrome tubular aggregate myopathy 1 uveitis
4978	opioid binding protein/cell adhesion molecule like	OPCML Aliases: IGLON1 IgLON family member 1 OBCAM OPCM	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma adenocarcinoma adenoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cholangiocarcinoma congenital heart disease cribriform carcinoma depressive disorder dermoid cyst of ovary distal arthrogryposis dysgerminoma embryoma esophagus squamous cell carcinoma gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma idiopathic scoliosis intrahepatic cholangiocarcinoma liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder melancholic depression mixed glioma nasopharynx carcinoma neurotic disorder nicotine dependence obsolete melancholia obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma prostate lymphoma sarcomatoid carcinoma schizophrenia steatotic liver disease stomach cancer stomach carcinoma tubular adenocarcinoma urinary bladder cancer
4973	oxidized low density lipoprotein receptor 1	OLR1 Aliases: CLEC8A LOX-1 SCARE1	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 Kawasaki disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis acute chest syndrome acute myocardial infarction adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation bone osteosarcoma brain stem infarction breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease carpal tunnel syndrome central sleep apnea cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma choriocarcinoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma end stage renal disease endomyocardial fibrosis essential hypertension familial hypercholesterolemia familial hyperlipidemia gallbladder disease generalized atherosclerosis gestational diabetes giant cell glioblastoma glioblastoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hyperhomocysteinemia hypertension hypertrophic cardiomyopathy juvenile rheumatoid arthritis keratitis keratoconjunctivitis kidney failure large intestine cancer liver cancer liver disease lung adenocarcinoma lung cancer multiple sclerosis multiple system atrophy myocardial infarction nutmeg liver obesity osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma parapsoriasis placenta cancer postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole renal osteodystrophy rheumatoid arthritis seborrheic keratosis sickle cell anemia silent myocardial infarction skin disease transient cerebral ischemia tubular adenocarcinoma type 2 diabetes mellitus vascular disease vertebrobasilar insufficiency
4968	8-oxoguanine DNA glycosylase	OGG1 Aliases: 8-hydroxyguanine DNA glycosylase HMMH HOGG1 MUTM OGG1 type 1d OGG1 type 1e OGG1 type 1g OGG1 type 1h OGH1	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 Barrett's esophagus Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Holt-Oram syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Trenaunay syndrome Langerhans-cell histiocytosis Marfan 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 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Rubinstein-Taybi syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia VACTERL association Werner syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute chest syndrome acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adult hepatocellular carcinoma age related macular degeneration allergic asthma anal carcinoma in situ angiomyolipoma angle-closure glaucoma anthracosilicosis anthracosis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial infectious disease bacterial meningitis basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder transitional cell papilloma bone marrow cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cataract central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism distal arthrogryposis duodenum disease dysthymic disorder embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exocrine pancreatic insufficiency familial adenomatous polyposis 1 familial adenomatous polyposis female breast carcinoma follicular adenoma follicular lymphoma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gallbladder disease gastric cardia adenocarcinoma gastric diffuse adenocarcinoma gastrointestinal system cancer gestational diabetes glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperglycemia hypertension hyperthyroidism idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor keratosis kidney angiomyolipoma kidney cancer kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leiomyoma leukemia liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus nephritis lymphoma macular degeneration major depressive disorder male infertility melancholic depression melanoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia with limb anomalies middle cerebral artery infarction mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelodysplastic syndrome myeloid sarcoma myeloproliferative neoplasm myocardial infarction myofibroma nail-patella syndrome nasopharynx carcinoma nephritis nephroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete ymphosarcoma oral mucosa leukoplakia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis pre-eclampsia primary angle-closure glaucoma primary open angle glaucoma prion disease progeria progressive supranuclear palsy propionic acidemia prostate cancer prostate carcinoma pterygium pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis senile cataract silent myocardial infarction situs inversus skin benign neoplasm skin cancer skin disease skin melanoma split hand-foot malformation 1 with sensorineural hearing loss sporadic breast cancer squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomach disease systemic lupus erythematosus thrombocytopenia-absent radius syndrome thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicocele vertebrobasilar insufficiency viral meningitis white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
4967	oxoglutarate dehydrogenase	OGDH Aliases: E1k KGD1 OGDC-E1 OGDH2	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 Creutzfeldt-Jakob disease Laron syndrome Leigh disease Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome achondroplasia alternating hemiplegia of childhood arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer cancer central nervous system disease cerebral degeneration colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease embryoma hydrocephalus lactic acidosis large intestine cancer lingual-facial-buccal dyskinesia movement disease nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus oxoglutarate dehydrogenase deficiency phenylketonuria placental insufficiency primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency senile degeneration of brain status epilepticus urea cycle disorder viral infectious disease
4952	OCRL inositol polyphosphate-5-phosphatase	OCRL Aliases: Dent disease 2 Dent-2 OCRL1	Homo sapiens (human)	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy
4938	2'-5'-oligoadenylate synthetase 1	OAS1	Homo sapiens (human)	primary immunodeficiency disease
4913	nth like DNA glycosylase 1	NTHL1 Aliases: NTH1 OCTS3	Homo sapiens (human)	B-cell lymphoma Fanconi anemia complementation group D2 Fanconi anemia Langerhans-cell histiocytosis acoustic neuroma actinic keratosis adenocarcinoma adenoma angiomatous meningioma autosomal recessive intellectual developmental disorder basal cell carcinoma benign meningioma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma clear cell meningioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatosis papulosa nigra duodenum adenocarcinoma embryoma endometrial cancer endometrial carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 3 familial adenomatous polyposis fibrous meningioma follicular adenoma intraorbital meningioma intraventricular meningioma inverted follicular keratosis islet cell tumor large intestine cancer laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma melanoacanthoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma non-Hodgkin lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cyst pancreatic adenocarcinoma papillary adenoma parasagittal meningioma pituitary adenoma psammomatous meningioma rectal benign neoplasm rectum cancer reticulosarcoma sarcomatoid carcinoma seborrheic dermatitis seborrheic keratosis secretory meningioma skin benign neoplasm skin cancer skin disease spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma transitional meningioma tuberous sclerosis 2 tuberous sclerosis urinary bladder cancer uterine corpus cancer
4907	5'-nucleotidase ecto	NT5E Aliases: CALJA CD73 eN eNT	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 Baraitser-Winter syndrome Chagas disease Crohn's colitis Crohn's disease Down syndrome Fabry disease Fraser syndrome 1 Fraser syndrome Gilbert syndrome Goldenhar syndrome Goodpasture syndrome Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Jervell-Lange Nielsen syndrome Kallmann syndrome MHC class II deficiency Meniere's disease Moebius syndrome Muckle-Wells syndrome Muenke Syndrome Nance-Horan syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Takayasu's arteritis Troyer syndrome Turner syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome X-linked agammaglobulinemia acinar cell carcinoma acoustic neuroma acute lymphoblastic leukemia acute maxillary sinusitis acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosine deaminase deficiency adult acute lymphocytic leukemia adult epithelioid sarcoma adult lymphoma adult medulloblastoma adult respiratory distress syndrome agammaglobulinemia allergic asthma allergic rhinitis amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 angiomatous meningioma angle-closure glaucoma ankylosing spondylitis anterior horn cell disease anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arterial tortuosity syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thyroiditis autosomal recessive distal hereditary motor neuronopathy 1 basal cell carcinoma benign meningioma benign mesothelioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma brain cancer branchiootic syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma calciphylaxis cancer carcinoma cardiac arrest cardiovascular system disease cecum adenocarcinoma celiac disease central nervous system cancer central nervous system origin vertigo cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood epithelioid sarcoma childhood leukemia childhood lymphoma childhood medulloblastoma cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic lymphocytic leukemia chronic maxillary sinusitis chronic obstructive pulmonary disease chronic rhinitis chylomicron retention disease clear cell meningioma clear cell renal cell carcinoma cleft palate colitis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital hemolytic anemia congenital hypogammaglobulinemia congenital nystagmus congestive heart failure connective tissue disease corneal disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma depressive disorder diffuse large B-cell lymphoma dissociated nystagmus double outlet right ventricle dysthymic disorder embryoma encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis enthesopathy epilepsy esophagitis esophagus squamous cell carcinoma eunuchism fibromyalgia fibrous meningioma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gastritis gastroenteritis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma gonadal dysgenesis granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hepatitis hepatocellular carcinoma hereditary arterial and articular multiple calcification syndrome high grade glioma hydrocephalus hyperthyroidism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated cleft palate isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoconus keratosis follicularis kidney cancer large intestine cancer laryngeal disease laryngeal squamous cell carcinoma lateral sclerosis lipid storage disease liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma major depressive disorder malignant mesothelioma mastoiditis maxillary sinusitis medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma mongolian spot motor neuron disease mucocele of salivary gland mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis myocardial infarction neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder newborn respiratory distress syndrome non-suppurative otitis media nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea olfactory groove meningioma orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pathologic nystagmus peptic esophagitis pericarditis periodontitis peripheral nervous system disease peripheral vascular disease pituitary adenoma polyarteritis nodosa polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum psoriasis pulmonary fibrosis pustulosis of palm and sole pycnodysostosis rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma secretory meningioma senile degeneration of brain sensorineural hearing loss septooptic dysplasia severe combined immunodeficiency sickle cell anemia silent myocardial infarction skin melanoma spinal meningioma spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma suppurative periapical periodontitis thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tonsillitis tracheal disease transitional meningioma trypanosomiasis tuberculosis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer vasculitis vasomotor rhinitis visual epilepsy
4886	neuropeptide Y receptor Y1	NPY1R	Homo sapiens (human)	amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy

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