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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **422026 - 422050** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
1141	cholinergic receptor nicotinic beta 2 subunit	CHRNB2	Homo sapiens (human)
1140	cholinergic receptor nicotinic beta 1 subunit	CHRNB1	Homo sapiens (human)
1139	cholinergic receptor nicotinic alpha 7 subunit	CHRNA7	Homo sapiens (human)
1138	cholinergic receptor nicotinic alpha 5 subunit	CHRNA5	Homo sapiens (human)
1137	cholinergic receptor nicotinic alpha 4 subunit	CHRNA4	Homo sapiens (human)
1136	cholinergic receptor nicotinic alpha 3 subunit	CHRNA3	Homo sapiens (human)
1135	cholinergic receptor nicotinic alpha 2 subunit	CHRNA2	Homo sapiens (human)
1134	cholinergic receptor nicotinic alpha 1 subunit	CHRNA1	Homo sapiens (human)
1133	cholinergic receptor muscarinic 5	CHRM5	Homo sapiens (human)
1132	cholinergic receptor muscarinic 4	CHRM4	Homo sapiens (human)
1131	cholinergic receptor muscarinic 3	CHRM3	Homo sapiens (human)
1130	lysosomal trafficking regulator	LYST	Homo sapiens (human)
1129	cholinergic receptor muscarinic 2	CHRM2	Homo sapiens (human)
1128	cholinergic receptor muscarinic 1	CHRM1	Homo sapiens (human)
1122	CHM like Rab escort protein	CHML	Homo sapiens (human)
1121	CHM Rab escort protein	CHM	Homo sapiens (human)
1120	choline kinase beta	CHKB Aliases: CHETK	Homo sapiens (human)	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder 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 distal myopathy epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder intellectual disability isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy nemaline myopathy 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 oculopharyngeal muscular dystrophy recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
1119	choline kinase alpha	CHKA Aliases: CKI	Homo sapiens (human)	Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 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 basal cell carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer colon adenoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma epilepsy esophagus squamous cell carcinoma facioscapulohumeral muscular dystrophy gliosarcoma hematologic cancer hepatitis B hepatocellular carcinoma high grade glioma large intestine cancer limb-girdle muscular dystrophy liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma megaconial type congenital muscular dystrophy microcephaly microphthalmia mixed glioma muscular dystrophy myelomeningocele myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma 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 oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma rippling muscle disease 2 spina bifida squamous cell carcinoma steatotic liver disease tethered spinal cord syndrome tongue squamous cell carcinoma transient cerebral ischemia vertebrobasilar insufficiency
1118	chitinase 1	CHIT1 Aliases: CHI3 CHIT chitotriosidase	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 Bloch-Sulzberger syndrome Creutzfeldt-Jakob disease Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Wolman disease acute myeloid leukemia adrenoleukodystrophy alkaptonuria allergic asthma allergic rhinitis amyloidosis amyotrophic lateral sclerosis ancylostomiasis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis aspartylglucosaminuria asthma atherosclerosis bacterial sepsis beta thalassemia bone marrow cancer breast cancer breast carcinoma cancer carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease childhood type dermatomyositis cholestasis chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency coronary artery disease cryptococcosis cystic fibrosis dementia dermatomyositis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia eumycotic mycetoma familial combined hyperlipidemia familial mediterranean fever filariasis follicular lymphoma frontotemporal dementia fucosidosis gastritis glomerulonephritis glycoproteinosis hepatitis C hypomelanosis of Ito idiopathic interstitial pneumonia interstitial lung disease intrinsic asthma juvenile rheumatoid arthritis kidney disease large intestine cancer lipid storage disease liver cirrhosis lung disease lysosomal acid lipase deficiency lysosomal storage disease malaria mevalonic aciduria multiple sclerosis myelofibrosis myeloproliferative neoplasm nephritis nephrosis neurodegenerative disease neuropathy nodal marginal zone lymphoma nutmeg liver obesity obstructive sleep apnea ochronosis osteoarthritis peripheral nervous system disease plasmacytoma polycythemia vera polycythemia polyneuropathy postinflammatory pulmonary fibrosis progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pulmonary fibrosis pyoureter sarcoidosis sialuria sickle cell anemia sphingolipidosis steatotic liver disease thalassemia tuberculosis type 2 diabetes mellitus uveoparotid fever vascular dementia vasomotor rhinitis
1117	chitinase 3 like 2	CHI3L2 Aliases: YKL-39 YKL39	Homo sapiens (human)	amyotrophic lateral sclerosis arthritis arthropathy breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma osteoarthritis papillary renal cell carcinoma progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
1116	chitinase 3 like 1	CHI3L1 Aliases: GP39 YK-40 YKL40 cartilage glycoprotein-39	Homo sapiens (human)	Alexander disease 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 CD40 ligand deficiency Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Gaucher's disease Goodpasture syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hantavirus hemorrhagic fever with renal syndrome Hermansky-Pudlak syndrome 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 Kawasaki disease Kuhnt-Junius degeneration Lafora disease Lewy body dementia Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Takayasu's arteritis X-linked hyper IgM syndrome acne acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute chest syndrome acute disseminated encephalomyelitis acute interstitial pneumonia acute kidney tubular necrosis acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia adult oligodendroglioma age related macular degeneration agnosia alcoholic liver cirrhosis allergic asthma allergic rhinitis alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis anaplastic astrocytoma androgen insensitivity syndrome anemia anthracosilicosis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis atopic dermatitis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bacterial infectious disease bacterial meningitis bacterial pneumonia bacterial sepsis benign ependymoma bipolar disorder bladder urothelial carcinoma blind loop syndrome bone disease bone marrow cancer bone osteosarcoma brain infarction breast cancer breast carcinoma bronchiolitis obliterans bronchitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer cardiovascular system disease carotid artery disease cartilage disease cataract 32 multiple types cellular ependymoma central nervous system cancer central nervous system disease cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia childhood oligodendroglioma childhood osteosarcoma childhood type dermatomyositis chondrosarcoma chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma cystic fibrosis degeneration of macula and posterior pole dementia depressive disorder dermatitis dermatomyositis diabetes mellitus diabetic ketoacidosis diabetic macular edema dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma eosinophilic pneumonia epilepsy esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exfoliation syndrome extrinsic allergic alveolitis farmer's lung fatal familial insomnia fibrillary astrocytoma follicular adenoma frontotemporal dementia gallbladder disease gastroenteritis gastrointestinal system cancer gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma granulomatosis with polyangiitis heart disease hematologic cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis high grade glioma human immunodeficiency virus infectious disease hyper IgM syndrome hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunodeficiency with hyper IgM type 3 inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome intermittent claudication interstitial lung disease intrahepatic cholestasis of pregnancy intrinsic asthma invasive ductal carcinoma juvenile pilocytic astrocytoma keratitis keratoconjunctivitis kidney disease large intestine cancer lichen planus liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma macrocytic anemia macular degeneration major depressive disorder malaria malignant astrocytoma melancholic depression melanoma meningitis microcystic adenoma middle cerebral artery infarction mitral valve stenosis mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma multiple sclerosis myelitis myelofibrosis myeloproliferative neoplasm myocardial infarction myositis myotonic dystrophy type 1 myotonic dystrophy type 2 myxopapillary ependymoma nephritis nephrosis nervous system disease neurodegenerative disease neurogenic arthropathy nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea oligodendroglioma oophoritis osteoarthritis osteoblastoma osteomyelitis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary ependymoma papillary renal cell carcinoma parametritis parapsoriasis pelvic inflammatory disease peripheral artery disease peripheral vascular disease pilocytic astrocytoma plasmacytoma pneumonia polyarteritis nodosa polycythemia vera polycythemia pompholyx portal vein thrombosis post-vaccinal encephalitis postinflammatory pulmonary fibrosis pre-eclampsia prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma primary pulmonary hypertension prion disease progressive muscular atrophy progressive supranuclear palsy prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis psychotic disorder pulmonary alveolar proteinosis pulmonary emphysema pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pustulosis of palm and sole pyosalpinx pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal detachment retinal disease retinitis retrograde amnesia rheumatoid arthritis salpingitis sarcoidosis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma scoliosis seborrheic keratosis sepiapterin reductase deficiency sick sinus syndrome silent myocardial infarction skin disease skin melanoma small cell carcinoma speech-language disorder-1 squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic scleroderma tanycytic ependymoma tauopathy temporal arteritis thrombophilia thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uveoparotid fever vascular dementia vascular disease vasomotor rhinitis viral pneumonia
1114	chromogranin B	CHGB	Homo sapiens (human)
1113	chromogranin A	CHGA Aliases: PHE5 PHES pancreastatin parastatin parathyroid secretory protein 1 vasostatin	Homo sapiens (human)	Clostridium difficile colitis Creutzfeldt-Jakob disease Ewing sarcoma IgA glomerulonephritis Peutz-Jeghers syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult lymphoma amyotrophic lateral sclerosis anxiety disorder aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation atrophic gastritis bladder carcinoma breast cancer breast carcinoma cancer carcinoma cerebral primitive neuroectodermal tumor cervix small cell carcinoma childhood angiosarcoma childhood lymphoma chronic fatigue syndrome chronic kidney disease colitis collagenous colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dermatitis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer embryoma encephalitis encephalomyelitis end stage renal disease endocrine gland cancer esophageal cancer esophageal carcinoma essential hypertension familial adenomatous polyposis follicular adenoma gastrinoma gastroenteritis generalized anxiety disorder granular cell carcinoma heart cancer hypertension hypoglycemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease insulinoma intermediate coronary syndrome irritable bowel syndrome islet cell tumor kidney failure large intestine cancer lung cancer lung disease lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphocytic colitis medulloblastoma medulloepithelioma microcystic adenoma multiple sclerosis myelitis myocardial infarction nephrosclerosis neuroblastoma neurocirculatory asthenia neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor obesity obsolete dyspepsia obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteoarthritis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma paraganglioma periodontitis pheochromocytoma phobic disorder pineal gland cancer pineoblastoma progressive muscular atrophy prolactinoma prostate cancer prostate carcinoma pulmonary embolism pulmonary large cell neuroendocrine carcinoma renal hypertension sarcomatoid carcinoma schizophrenia silent myocardial infarction small intestine cancer squamous cell carcinoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor thyroid gland medullary carcinoma tongue squamous cell carcinoma transitional cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis ureter small cell carcinoma urinary bladder cancer von Hippel-Lindau disease
1112	forkhead box N3	FOXN3	Homo sapiens (human)
1111	checkpoint kinase 1	CHEK1	Homo sapiens (human)

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