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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 **9576 - 9600** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
865	core-binding factor subunit beta	CBFB	Homo sapiens (human)
864	RUNX family transcription factor 3	RUNX3	Homo sapiens (human)
862	RUNX1 partner transcriptional co-repressor 1	RUNX1T1	Homo sapiens (human)
861	RUNX family transcription factor 1	RUNX1	Homo sapiens (human)
860	RUNX family transcription factor 2	RUNX2	Homo sapiens (human)
847	catalase	CAT	Homo sapiens (human)	46,XY sex reversal 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 Behcet's disease Bloom syndrome Burkitt lymphoma Carney complex Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Clostridium difficile colitis Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Crimean-Congo hemorrhagic fever Down syndrome Dubowitz syndrome Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Graves ophthalmopathy Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hailey-Hailey disease Hantavirus hemorrhagic fever with renal syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis Leber hereditary optic neuropathy Marfan syndrome Meesmann corneal dystrophy Miles-Carpenter 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 Raynaud disease Refsum disease Rett syndrome Reye syndrome Robinow syndrome Rothmund-Thomson syndrome Scheie syndrome Seckel syndrome Silver-Russell syndrome St. Louis encephalitis Sveinsson chorioretinal atrophy T-cell acute lymphoblastic leukemia Turner syndrome WAGR syndrome Werner syndrome Wernicke-Korsakoff syndrome Wilson disease Wolman disease X-linked Aarskog syndrome X-linked chronic granulomatous disease Zellweger syndrome Zika fever abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acatalasia acne acoustic neuroma acquired hyperkeratosis acrodermatitis actinic keratosis actinomycosis acute cholangitis acute intermittent porphyria acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adenosarcoma adrenal gland cancer adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome age related macular degeneration agenesis of the corpus callosum with peripheral neuropathy aggressive systemic mastocytosis agnosia alcohol dependence alcohol use disorder alcoholic liver cirrhosis allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis alpha 1-antitrypsin deficiency amnestic disorder amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anemia angioedema angle-closure glaucoma animal phobia aniridia ankylosing spondylitis anterior horn cell disease anterolateral myocardial infarction anteroseptal myocardial infarction anthracosilicosis anthracosis antisocial personality disorder anxiety disorder aortic aneurysm aortic disease aortic valve insufficiency aphthous stomatitis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis ascariasis ascaridiasis aspergillosis asphyxia neonatorum aspiration pneumonia aspiration pneumonitis asthma ataxia telangiectasia 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 autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cerebellar ataxia autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive distal hereditary motor neuronopathy 1 azoospermia background diabetic retinopathy bacterial infectious disease bacterial pneumonia bacterial sepsis basal cell carcinoma benign mesothelioma bestrophinopathy beta thalassemia bile duct adenocarcinoma bile duct carcinoma bipolar disorder black piedra bladder carcinoma blood coagulation disease bone marrow cancer bone osteosarcoma brain cancer brain disease brain infarction brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer carbamoyl phosphate synthetase I deficiency disease carcinoma cardiac arrest cardiomyopathy cardiovascular system disease cartilage-hair hypoplasia cataract cellular schwannoma central nervous system cancer central nervous system lymphoma central sleep apnea cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chondrodysplasia-pseudohermaphroditism syndrome choriocarcinoma choroid plexus papilloma chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic granulomatous disease chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic purulent otitis media chronic venous insufficiency clear cell renal cell carcinoma cleft palate coccidioidomycosis colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency congenital hemolytic anemia congenital hypothyroidism congestive heart failure corneal disease coronary artery disease coronary thrombosis cribriform carcinoma critical illness polyneuropathy cutaneous anthrax cutaneous leishmaniasis cutis laxa cystic fibrosis cystitis cystoid macular edema deficiency anemia degeneration of macula and posterior pole delusional disorder dengue disease denture stomatitis depressive disorder dermatitis developmental coordination disorder diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diffuse large B-cell lymphoma diffuse scleroderma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal arthrogryposis duodenum cancer duodenum disease dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endometritis endomyocardial fibrosis eosinophilia-myalgia syndrome epidermolysis bullosa dystrophica epilepsy erysipelas erythrasma esophageal disease essential hypertension extramedullary plasmacytoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial hyperlipidemia familial mediterranean fever familial periodic paralysis favism female stress incontinence fibrillary astrocytoma fibromyalgia focal epilepsy fragile X syndrome gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric ulcer gastritis gastroenteritis gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucocorticoid-remediable aldosteronism glucose intolerance goiter gonadal dysgenesis gonadoblastoma gonorrhea granular cell carcinoma granular corneal dystrophy 2 head and neck squamous cell carcinoma heart cancer heart disease hemiplegia hemochromatosis hemolytic-uremic syndrome hemopericardium hepatitis A hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 5 hereditary spherocytosis type 1 hereditary spherocytosis herpes simplex high grade glioma histoplasmosis holoprosencephaly 1 holoprosencephaly homocystinuria hyperglycemia hyperhomocysteinemia hypertension hyperthyroidism hypertrophic cardiomyopathy hyperuricemia hypochromic anemia hypothalamic disease hypothyroidism idiopathic interstitial pneumonia ileitis ileocolitis immune system disease inclusion body myositis infantile Refsum disease inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease insulinoma intellectual disability interstitial nephritis intestinal disease intrahepatic cholangiocarcinoma intraocular lymphoma intrinsic asthma iron metabolism disease irritable bowel syndrome isolated cleft palate juvenile pilocytic astrocytoma juvenile rheumatoid arthritis keratitis keratoacanthoma keratoconjunctivitis keratoconus keratosis kernicterus due to isoimmunization kernicterus kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer late onset Parkinson's disease lateral sclerosis learning disability lesion of sciatic nerve leukopenia lichen disease lichen planus lipid storage disease listeriosis liver cancer liver cirrhosis localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lymphoma lysosomal acid lipase deficiency macrocytic anemia macular corneal dystrophy macular degeneration macular retinal edema major depressive disorder mal de Meleda malaria male infertility malignant astrocytoma malignant mesothelioma marasmus mast-cell sarcoma melancholic depression melanoma melanotic neurilemmoma meningioma meningitis meningoencephalitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microcytic anemia middle cerebral artery infarction migraine with aura migraine without aura mitral valve stenosis mixed glioma mixed oligodendroglioma-astrocytoma mood disorder motor neuron disease motor peripheral neuropathy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis multiple myeloma multiple sclerosis myelitis myelofibrosis myeloproliferative neoplasm myocardial infarction myocardial stunning myopathy myotonic dystrophy type 1 myxedema neonatal jaundice neovascular inflammatory vitreoretinopathy nephritis nephroblastoma nephrolithiasis nephrosis neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibromatosis neuropathy neurotic disorder newborn respiratory distress syndrome nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive lung disease optic neuritis osteoarthritis osteoglophonic dysplasia osteonecrosis osteoporosis osteosarcoma otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma papilloma parapsoriasis parathyroid gland disease parietal foramina partial motor epilepsy patent foramen ovale pemphigus pericardial effusion pericarditis perinatal necrotizing enterocolitis periodontal disease periodontitis peripheral nervous system disease peroxisomal disease peroxisome biogenesis disorder 1A peroxisome biogenesis disorder 7A peroxisome biogenesis disorder 8A personality disorder phenylketonuria pheochromocytoma phobic disorder photosensitive trichothiodystrophy phototoxic dermatitis pilocytic astrocytoma pituitary adenoma pityriasis rubra pilaris placenta cancer placental insufficiency plasmacytoma plexiform schwannoma pneumoconiosis pneumonia polycystic ovary syndrome polycythemia vera polyneuropathy post-traumatic stress disorder postinflammatory pulmonary fibrosis prediabetes syndrome preretinal fibrosis primary angle-closure glaucoma primary open angle glaucoma proctitis progeria progressive multifocal leukoencephalopathy progressive muscular atrophy proliferative diabetic retinopathy prostate cancer prostate carcinoma prostate disease prostatic adenoma protein-energy malnutrition protoplasmic astrocytoma pseudoxanthoma elasticum psoriasis pterygium pulmonary edema pulmonary embolism pulmonary emphysema pulmonary fibrosis purpura pustulosis of palm and sole pyelitis pyelonephritis pyoureter recessive dystrophic epidermolysis bullosa renal artery disease renal carcinoma renal cell carcinoma restrictive dermopathy reticulosarcoma retinal disease retinitis pigmentosa retinitis retinopathy of prematurity retrograde amnesia rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma scabies schizophrenia sciatic neuropathy scleroderma sebaceous carcinoma seborrheic dermatitis senile cataract sensorineural hearing loss sick sinus syndrome sickle cell anemia silent myocardial infarction situs inversus skin atrophy skin benign neoplasm skin cancer skin melanoma small intestine cancer social phobia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy specific phobia spinal muscular atrophy spinal stenosis spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spondylocarpotarsal synostosis syndrome sporotrichosis squamous cell carcinoma squamous cell papilloma status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomach disease stomatitis subacute bacterial endocarditis subependymal giant cell astrocytoma superficial mycosis superior mesenteric artery syndrome suppurative otitis media sweat gland cancer systemic lupus erythematosus systemic scleroderma teratocarcinoma thrombocytopenia thrombophilia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma toxic encephalopathy transient cerebral ischemia trigonitis tuberculosis tuberous sclerosis tubular adenocarcinoma tympanosclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ulcerative stomatitis urea cycle disorder uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer urticaria uterine corpus cancer uveoparotid fever varicocele variegate porphyria vascular disease vasomotor rhinitis vertebrobasilar insufficiency vestibular schwannomatosis viral infectious disease visual epilepsy vitiligo white piedra 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 yellow fever
846	calcium sensing receptor	CASR	Homo sapiens (human)
845	calsequestrin 2	CASQ2	Homo sapiens (human)
844	calsequestrin 1	CASQ1	Homo sapiens (human)
842	caspase 9	CASP9	Homo sapiens (human)
840	caspase 7	CASP7	Homo sapiens (human)
839	caspase 6	CASP6	Homo sapiens (human)
833	cysteinyl-tRNA synthetase 1	CARS1	Homo sapiens (human)
832	capping actin protein of muscle Z-line subunit beta	CAPZB	Homo sapiens (human)
831	calpastatin	CAST	Homo sapiens (human)
829	capping actin protein of muscle Z-line subunit alpha 1	CAPZA1	Homo sapiens (human)
828	calcyphosine	CAPS	Homo sapiens (human)
826	calpain small subunit 1	CAPNS1	Homo sapiens (human)
825	calpain 3	CAPN3	Homo sapiens (human)
823	calpain 1	CAPN1	Homo sapiens (human)
822	capping actin protein, gelsolin like	CAPG	Homo sapiens (human)
821	calnexin	CANX Aliases: CNX IP90 P90 major histocompatibility complex class I antigen-binding protein p88	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Lyme disease MASA syndrome Marfan syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 absence epilepsy acute myocardial infarction adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system lymphoma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood absence epilepsy childhood medulloblastoma childhood osteosarcoma cone-rod dystrophy coronary artery disease coronary thrombosis diabetes mellitus diabetic angiopathy diabetic ketoacidosis embryoma exanthema subitum fundus albipunctatus giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperinsulinism interstitial lung disease keratosis follicularis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mongolian spot monoclonal gammopathy of uncertain significance motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma multiple sclerosis myocardial infarction nephrogenic diabetes insipidus neuropathy nodular prostate obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum oculocutaneous albinism type IA oculocutaneous albinism osteosarcoma peripheral nervous system disease platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 polyneuropathy post-traumatic stress disorder progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pseudoachondroplasia pseudoxanthoma elasticum renal tubular acidosis retinitis pigmentosa rubella silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus vitiligo von Willebrand's disease
820	cathelicidin antimicrobial peptide	CAMP	Homo sapiens (human)
818	calcium/calmodulin dependent protein kinase II gamma	CAMK2G	Homo sapiens (human)
817	calcium/calmodulin dependent protein kinase II delta	CAMK2D	Homo sapiens (human)

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