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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 **1776 - 1800** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
342372	polycystin 1 like 3, transient receptor potential channel interacting	PKD1L3	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease cerebral infarction cerebrovascular disease episodic kinesigenic dyskinesia 1 prostate cancer prostate carcinoma
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
1579	cytochrome P450 family 4 subfamily A member 11	CYP4A11 Aliases: CYP4AII	Homo sapiens (human)	Meckel syndrome acute myocardial infarction alcoholic liver cirrhosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease brain stem infarction cancer cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis embryoma essential hypertension hepatocellular carcinoma hypertension liver cancer liver cirrhosis myocardial infarction nephrosclerosis nutmeg liver renal artery disease renal hypertension silent myocardial infarction steatotic liver disease varicose veins
79053	ALG8 alpha-1,3-glucosyltransferase	ALG8 Aliases: MGC2840 dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 anemia asphyxia neonatorum autosomal dominant polycystic kidney disease cataract cholestasis clubfoot congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism cryptorchidism cystic kidney disease depressive disorder developmental and epileptic encephalopathy 36 diarrhea dysthymic disorder elephantiasis gastrointestinal system disease heart septal defect hypothyroidism intestinal disease lymphedema macrocytic anemia major depressive disorder melancholic depression myxedema neurotic disorder non-congenital cyst of kidney obsolete melancholia oligohydramnios patent ductus arteriosus placental insufficiency polycystic liver disease polyhydramnios protein-losing enteropathy thrombocytopenia
378	ADP ribosylation factor 4	ARF4	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease breast cancer cystic kidney disease giant cell glioblastoma glioblastoma hepatitis C high grade glioma ovarian cancer ovarian carcinoma
277	amylase alpha 1B	AMY1B	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
278	amylase alpha 1C	AMY1C	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
276	amylase alpha 1A	AMY1A	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition schizophrenia seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
23213	sulfatase 1	SULF1 Aliases: Extracellular sulfatase Sulf-1 KIAA1077 SULF-1 hSulf-1	Homo sapiens (human)	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
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
23443	solute carrier family 35 member A3	SLC35A3 Aliases: UDP-N-acetylglucosamine transporter	Homo sapiens (human)	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
51604	phosphatidylinositol glycan anchor biosynthesis class T	PIGT Aliases: GPI transamidase component PIG-T GPI transamidase subunit PIG-T	Homo sapiens (human)	Marfan syndrome angioedema blindness brain disease breast cancer breast carcinoma calcinosis calcium metabolism disease cerebral degeneration congenital nystagmus craniosynostosis cystic kidney disease dermatographia diarrhea dissociated nystagmus epilepsy esotropia fibromyalgia hemolytic anemia hypercalcemia hyperopia hypertropia hypophosphatasia mechanical strabismus monocular esotropia multiple congenital anomalies-hypotonia-seizures syndrome 3 myositis nephrocalcinosis non-congenital cyst of kidney ophthalmoplegia osteoporosis paroxysmal nocturnal hemoglobinuria patent ductus arteriosus pathologic nystagmus phosphorus metabolism disease restrictive cardiomyopathy scoliosis situs inversus spontaneous ocular nystagmus strabismus tuberous sclerosis urticaria visual epilepsy
9524	trans-2,3-enoyl-CoA reductase	TECR Aliases: MRT14 TER very-long-chain enoyl-CoA reductase	Homo sapiens (human)	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
139189	diacylglycerol kinase kappa	DGKK	Homo sapiens (human)	Marfan syndrome agnosia arteriosclerotic cardiovascular disease atherosclerosis conduct disorder coronary artery disease developmental coordination disorder disease of mental health fragile X syndrome hepatocellular carcinoma hypospadias liver cancer prostate cancer prostate carcinoma situs inversus syndromic X-linked intellectual disability 94 tuberous sclerosis
22845	dolichol kinase	DOLK Aliases: DK1 KIAA1094 dolichol kinase 1	Homo sapiens (human)	Marfan syndrome X-linked dilated cardiomyopathy autosomal recessive polycystic kidney disease congenital disorder of glycosylation Im congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dilated cardiomyopathy 1A 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 ichthyosis isolated elevated serum creatine phosphokinase levels lipoatrophic diabetes mellitus lipodystrophy nonepidermolytic palmoplantar keratoderma palmoplantar keratosis polycystic kidney disease 4 sensorineural hearing loss situs inversus tuberous sclerosis
3631	inositol polyphosphate-4-phosphatase type I A	INPP4A Aliases: Type I inositol 3,4-bisphosphate 4-phosphatase	Homo sapiens (human)	Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma autosomal dominant dyskeratosis congenita 1 bladder carcinoma cancer early myoclonic encephalopathy embryoma intrinsic asthma lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma situs inversus tuberous sclerosis urinary bladder cancer
347527	arylsulfatase family member H	ARSH	Homo sapiens (human)	Marfan syndrome Richter's syndrome X-linked chondrodysplasia punctata 1 acquired immunodeficiency syndrome acrodermatitis alcoholic liver cirrhosis autosomal dominant chondrodysplasia punctata cancer childhood leukemia chondrodysplasia punctata chronic lymphocytic leukemia dermatitis dyschromatosis symmetrica hereditaria essential thrombocythemia gallbladder disease hepatitis human immunodeficiency virus infectious disease leukemia liver cirrhosis liver disease microphthalmia mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis myelodysplastic syndrome neuroblastoma obsolete Matthew-Wood syndrome oculocerebrorenal syndrome rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 situs inversus tuberous sclerosis ventricular septal defect
6309	sterol-C5-desaturase	SC5D Aliases: delta(7)-sterol 5(6)-desaturase lathosterol oxidase	Homo sapiens (human)	Marfan syndrome Peters anomaly Smith-Lemli-Opitz syndrome Unverricht-Lundborg syndrome basal cell carcinoma blepharospasm cataract cleft palate clubfoot complex partial epilepsy congenital heart disease congenital ptosis cornea plana early myoclonic encephalopathy epilepsy focal hand dystonia gallbladder disease gingival hypertrophy gingival overgrowth intellectual disability intrahepatic cholestasis isolated cleft palate learning disability liver disease meningocele microcephaly placental insufficiency polydactyly ptosis sensorineural hearing loss situs inversus temporal lobe epilepsy thrombocytopenia tuberous sclerosis visual epilepsy
126	alcohol dehydrogenase 1C (class I), gamma polypeptide	ADH1C	Homo sapiens (human)	Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult hepatocellular carcinoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood hepatocellular carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma follicular adenoma gallbladder disease gemistocytic astrocytoma glucose intolerance granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemorrhoid hepatocellular carcinoma high grade glioma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder malignant astrocytoma melancholic depression microcystic adenoma myocardial infarction neurotic disorder nicotine dependence nutmeg liver obsolete constipation obsolete melancholia oropharynx cancer pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma pharynx cancer pilocytic astrocytoma prediabetes syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma secondary Parkinson disease silent myocardial infarction situs inversus squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
125	alcohol dehydrogenase 1B (class I), beta polypeptide	ADH1B	Homo sapiens (human)	Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wernicke-Korsakoff syndrome acute myocardial infarction acute pancreatitis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic neuropathy alcoholic pancreatitis allergic asthma allergic rhinitis amnestic disorder anaplastic astrocytoma anemia antisocial personality disorder anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma corneal disease coronary artery disease coronary thrombosis degenerative disc disease depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder embryoma enthesopathy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential tremor exostosis fibrillary astrocytoma flat ductal epithelial atypia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatocellular carcinoma heroin dependence high grade glioma hyperphosphatemia hypertension hypopharynx cancer intrinsic asthma juvenile pilocytic astrocytoma keratoconus large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer leukopenia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia macrocytic anemia major depressive disorder malaria malignant astrocytoma melancholic depression migraine morphine dependence myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia opiate dependence oral cavity cancer oropharynx cancer ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis parapsoriasis periarthritis personality disorder pharynx cancer pilocytic astrocytoma placental insufficiency protoplasmic astrocytoma psoriasis psychotic disorder pustulosis of palm and sole restless legs syndrome schizoaffective disorder schizophreniform disorder silent myocardial infarction situs inversus squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma tendinitis thrombocytopenia tongue squamous cell carcinoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer vascular disease vasomotor rhinitis
5589	PRKCSH beta subunit of glucosidase II	PRKCSH	Homo sapiens (human)	Marfan syndrome Meckel syndrome autosomal dominant polycystic kidney disease beta thalassemia breast cancer breast carcinoma cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cystic kidney disease diabetic ketoacidosis episodic ataxia type 2 esophagitis familial hemiplegic migraine 1 familial hemiplegic migraine familial hypercholesterolemia gallbladder disease gastroesophageal reflux disease hepatitis B hepatocellular carcinoma liver cancer liver disease non-congenital cyst of kidney obsolete type 1 diabetes mellitus 9 peptic esophagitis polycystic kidney disease 1 polycystic liver disease situs inversus tuberous sclerosis 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
220	aldehyde dehydrogenase 1 family member A3	ALDH1A3 Aliases: RALDH3 retinaldehyde dehydrogenase 3	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome acoustic neuroma adenocarcinoma adenoma angiomatous meningioma autism spectrum disorder autistic disorder benign meningioma bilateral optic nerve hypoplasia bile duct adenocarcinoma bile duct carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral convexity meningioma choanal atresia cholangiocarcinoma clear cell meningioma coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma distal arthrogryposis embryoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrous meningioma gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma high grade glioma intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor isolated microphthalmia 1 isolated microphthalmia 2 isolated microphthalmia 3 isolated microphthalmia 4 isolated microphthalmia 6 isolated microphthalmia 7 isolated microphthalmia 8 large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma malignant pleural mesothelioma melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma neuroblastoma olfactory groove meningioma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma pituitary adenoma polycystic ovary syndrome prostate cancer prostate carcinoma psammomatous meningioma rheumatoid arthritis secretory meningioma seminoma situs inversus skin melanoma spinal meningioma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testicular germ cell cancer thyroid gland papillary carcinoma transitional meningioma transthyretin amyloidosis tuberous sclerosis tubular adenocarcinoma
5311	polycystin 2, transient receptor potential cation channel	PKD2 Aliases: PC2 PKD4 Pc-2 TRPP2 transient receptor potential cation channel, subfamily P, member 2	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Wiskott-Aldrich syndrome acute kidney failure adrenal gland cancer atrial fibrillation atrioventricular block autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cholangiocarcinoma chronic kidney disease ciliopathy collagen disease congenital heart disease congestive heart failure connective tissue disease cystic kidney disease disorder of sexual development distal arthrogryposis duodenum cancer embryoma episodic kinesigenic dyskinesia 1 essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis focal segmental glomerulosclerosis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gout heart cancer hermaphroditism high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intracranial aneurysm intrahepatic cholangiocarcinoma islet cell tumor kidney disease kidney failure laryngeal squamous cell carcinoma lung adenocarcinoma lung cancer mixed glioma nephritis nephrosis neurodegenerative disease non-congenital cyst of kidney pheochromocytoma placental insufficiency polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 4 polycystic kidney disease polycystic liver disease prostate cancer prostate carcinoma pseudohermaphroditism pyoureter retinal degeneration situs inversus small intestine cancer thoracic aortic aneurysm tuberous sclerosis uremia urinary bladder cancer
9945	glutamine-fructose-6-phosphate transaminase 2	GFPT2 Aliases: GFAT2 glutamine: fructose-6-phosphate aminotransferase 2	Homo sapiens (human)	Machado-Joseph disease acute myocardial infarction cancer chronic kidney disease coronary thrombosis diabetes mellitus embryoma hyperglycemia lung cancer lung non-small cell carcinoma myocardial infarction ovarian cancer ovarian carcinoma silent myocardial infarction type 2 diabetes mellitus
2137	exostosin like glycosyltransferase 3	EXTL3 Aliases: REG receptor REGR botv glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase	Homo sapiens (human)	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis

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