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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 **1226 - 1250** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
130749	carboxypeptidase O	CPO Aliases: metallocarboxypeptidase C metallocarboxypeptidase O	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
1368	carboxypeptidase M	CPM Aliases: renal carboxypeptidase urinary carboxypeptidase B	Homo sapiens (human)	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
51805	coenzyme Q3, methyltransferase	COQ3	Homo sapiens (human)
27235	coenzyme Q2, polyprenyltransferase	COQ2	Homo sapiens (human)	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
1312	catechol-O-methyltransferase	COMT	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 Balo concentric sclerosis Clostridium difficile colitis Cockayne syndrome DiGeorge syndrome Dowling-Degos disease Down syndrome Gilles de la Tourette syndrome Graves' disease Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kleine-Levin syndrome Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Lynch syndrome Meckel syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wolfram syndrome 1 Wolfram syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired immunodeficiency syndrome acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer adrenoleukodystrophy adult lymphoma agnosia alcohol dependence alcohol use disorder alexia allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anencephaly anorexia nervosa antisocial personality disorder anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis 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 attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autonomic neuropathy autosomal dominant polycystic kidney disease avoidant personality disorder bipolar disorder bladder carcinoma borderline personality disorder breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma bulimia nervosa bullous congenital ichthyosiform erythroderma cancer cannabis abuse cannabis dependence cardiovascular system disease carpal tunnel syndrome cataract central nervous system disease central nervous system lymphoma central nervous system origin vertigo central sleep apnea cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood disintegrative disease childhood kidney cell carcinoma childhood lymphoma choanal atresia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate clubfoot cocaine abuse cocaine dependence cognitive disorder collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus conduct disorder congenital diarrhea 5 with tufting enteropathy congenital hypothyroidism congenital ptosis conversion disorder corneal neovascularization coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma critical illness polyneuropathy cryptorchidism degenerative disc disease delusional disorder dementia dental caries dental fluorosis dentin caries depressive disorder desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health dissociative disorder distal myopathy double outlet right ventricle drug dependence drug psychosis duodenum cancer dyslexia dysthymic disorder dystonia eating disorder eclampsia embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epilepsy episodic kinesigenic dyskinesia 1 episodic kinesigenic dyskinesia 2 esophagitis esophagus squamous cell carcinoma essential hypertension eumycotic mycetoma female breast carcinoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroesophageal reflux disease generalized anxiety disorder glaucoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hepatitis C hepatocellular carcinoma heroin dependence herpes simplex holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hydrocephalus hypercalcemia hypertension hypertensive encephalopathy hyperthyroidism hypertropia hypoparathyroidism hypospadias hypothyroidism imperforate anus impulse control disorder inappropriate ADH syndrome inflammatory and toxic neuropathy inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma irritable bowel syndrome isolated cleft palate kidney cancer kleptomania large intestine cancer late onset Parkinson's disease lateral meningocele syndrome learning disability leiomyoma lingual-facial-buccal dyskinesia lissencephaly liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder male infertility mechanical strabismus melancholic depression meningoencephalitis microcephaly microglandular adenosis microphthalmia migraine without aura migraine mitral valve stenosis mood disorder morphine dependence multiple sclerosis myelitis myelomeningocele myeloproliferative disorder with eosinophilia myocardial infarction myofibroma myositis ossificans myositis myxedema narcissistic personality disorder narcolepsy neonatal abstinence syndrome nephrocalcinosis nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nicotine dependence nodular prostate non-Hodgkin lymphoma nutmeg liver obesity obsessive-compulsive disorder obsessive-compulsive personality disorder obsolete T-cell lymphoblastic leukemia/lymphoma obsolete constipation obsolete dyspepsia obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea omphalocele ophthalmoplegia opiate dependence optic atrophy osteoarthritis osteochondritis dissecans osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary renal cell carcinoma paranoid schizophrenia parapsoriasis patent ductus arteriosus patent foramen ovale pathological gambling peptic esophagitis peripheral nervous system disease pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency polycystic ovary syndrome polyhydramnios polyneuropathy post-traumatic stress disorder pre-eclampsia prediabetes syndrome premature ejaculation premature menopause primary immunodeficiency disease primary ovarian insufficiency progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism psoriasis psychotic disorder ptosis purpura pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent hypersomnia renal carcinoma renal cell carcinoma renal hypoplasia reticulate acropigmentation of Kitamura reticulosarcoma retrograde amnesia rumination disorder sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder schizotypal personality disorder scoliosis seasonal affective disorder seborrheic dermatitis seborrheic infantile dermatitis seborrheic keratosis secondary Parkinson disease senile degeneration of brain sickle cell anemia silent myocardial infarction small intestine cancer social phobia somatization disorder somatoform disorder spina bifida sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma strabismus subacute delirium substance abuse substance-related disorder systemic lupus erythematosus tethered spinal cord syndrome tetralogy of Fallot thrombocytopenia thrombophilia thyrotoxicosis tibial muscular dystrophy tongue squamous cell carcinoma transient myeloproliferative syndrome tricuspid atresia tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicose veins velocardiofacial syndrome ventricular septal defect vesicoureteral reflux visual epilepsy vitiligo withdrawal disorder 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
23127	collagen beta(1-O)galactosyltransferase 2	COLGALT2 Aliases: KIAA0584 Procollagen galactosyltransferase	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 bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
10584	collectin subfamily member 10	COLEC10 Aliases: CL-10 CL-L1	Homo sapiens (human)	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
1298	collagen type IX alpha 2 chain	COL9A2 Aliases: MED	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
1291	collagen type VI alpha 1 chain	COL6A1	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
84342	component of oligomeric golgi complex 8	COG8 Aliases: DOR1 FLJ22315	Homo sapiens (human)	Dandy-Walker syndrome Unverricht-Lundborg syndrome alternating esotropia alveolar soft part sarcoma blepharospasm brain disease clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIh congenital disorder of glycosylation developmental and epileptic encephalopathy 36 early myoclonic encephalopathy epilepsy esophageal cancer esophageal carcinoma focal hand dystonia hepatocellular carcinoma hydrocephalus hypoglycemia intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability liver cancer lung benign neoplasm lung carcinoma microcephaly protein-losing enteropathy scoliosis status epilepticus stomach cancer stomach carcinoma visual epilepsy
91949	component of oligomeric golgi complex 7	COG7	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
57511	component of oligomeric golgi complex 6	COG6 Aliases: COD2 KIAA1134	Homo sapiens (human)	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
10466	component of oligomeric golgi complex 5	COG5 Aliases: GTC90	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 Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy
25839	component of oligomeric golgi complex 4	COG4 Aliases: COD1 DKFZP586E1519	Homo sapiens (human)	Laron syndrome Saul-Wilson syndrome X-linked nonsyndromic deafness achondroplasia agnosia agranulocytosis apraxia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness blood coagulation disease cataract 5 multiple types cataract cerebral degeneration clubfoot cone-rod dystrophy congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIj congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness developmental coordination disorder dissociated nystagmus enophthalmos fundus albipunctatus microcephaly neutropenia night blindness obsolete autosomal recessive nonsyndromic deafness 105 obsolete exophthalmos obsolete inherited blood coagulation disease orbital disease pathologic nystagmus placental insufficiency retinitis pigmentosa 3 retinitis pigmentosa sensorineural hearing loss severe congenital neutropenia spontaneous ocular nystagmus thrombocytopenia
83548	component of oligomeric golgi complex 3	COG3 Aliases: SEC34	Homo sapiens (human)	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer congenital disorder of glycosylation type II
22796	component of oligomeric golgi complex 2	COG2	Homo sapiens (human)	atrial fibrillation cardiovascular system disease congenital disorder of glycosylation type IIq congenital disorder of glycosylation coronary artery disease diabetes mellitus epilepsy familial hypercholesterolemia heart disease hypobetalipoproteinemia locked-in syndrome obsolete constipation quadriplegia rheumatoid arthritis stomach cancer stomach carcinoma type 2 diabetes mellitus visual epilepsy
9382	component of oligomeric golgi complex 1	COG1 Aliases: KIAA1381	Homo sapiens (human)	Baraitser-Winter syndrome Burkitt lymphoma Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome anemia branchiootic syndrome cerebral degeneration cerebrocostomandibular syndrome chronic lymphocytic leukemia clubfoot congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIg cryptorchidism hematologic cancer hydronephrosis hypospadias kidney failure macrocytic anemia orofaciodigital syndrome I orofaciodigital syndrome X placental insufficiency primary pulmonary hypertension scoliosis sensorineural hearing loss thrombocytopenia
27255	contactin 6	CNTN6 Aliases: NB-3 neural adhesion molecule	Homo sapiens (human)	Gilles de la Tourette syndrome Hirschsprung's disease Parkinson's disease 2 acquired immunodeficiency syndrome adenoid cystic carcinoma alcohol dependence alcohol use disorder anorexia nervosa attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder breast cancer communicating hydrocephalus cone-rod dystrophy 2 cone-rod dystrophy differentiated thyroid gland carcinoma epilepsy hydrocephalus intellectual disability learning disability obstructive hydrocephalus ovarian carcinoma salivary gland adenoid cystic carcinoma schizophrenia senile degeneration of brain systemic lupus erythematosus
53942	contactin 5	CNTN5 Aliases: NB-2 hNB-2	Homo sapiens (human)	Behcet's disease Hirschsprung's disease Parkinson's disease 2 anorexia nervosa atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder communicating hydrocephalus congestive heart failure depressive disorder differentiated thyroid gland carcinoma essential hypertension gout hydrocephalus hypertension major depressive disorder melancholic depression neurotic disorder obsolete melancholia obstructive hydrocephalus primary biliary cholangitis schizophrenia senile degeneration of brain
152330	contactin 4	CNTN4 Aliases: BIG-2	Homo sapiens (human)	adrenal gland cancer alcohol dependence alcohol use disorder amyotrophic lateral sclerosis type 1 anorexia nervosa autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia autosomal recessive spinocerebellar ataxia 16 bilateral optic nerve hypoplasia bipolar disorder breast cancer breast carcinoma cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma disease of mental health duodenum cancer epilepsy essential hypertension gallbladder cancer gallbladder carcinoma heart cancer hypertension intellectual disability large intestine cancer learning disability obesity ovarian cancer ovarian carcinoma paraganglioma pheochromocytoma primary open angle glaucoma psychotic disorder schizophrenia small intestine cancer speech disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
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
6900	contactin 2	CNTN2 Aliases: TAG-1 TAX1	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 Gamstorp-Wohlfart syndrome Guillain-Barre syndrome Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Unverricht-Lundborg syndrome Van der Woude syndrome Wolff-Parkinson-White syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis adult T-cell leukemia/lymphoma adult lymphoma adult oligodendroglioma anaplastic astrocytoma arthritis arthropathy atrial fibrillation atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bladder carcinoma blepharospasm bone marrow disease bone osteosarcoma cancer central nervous system cancer central nervous system lymphoma cerebral degeneration childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood oligodendroglioma childhood osteosarcoma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy early myoclonic encephalopathy embryoma epilepsy episodic ataxia type 1 familial adult myoclonic epilepsy 5 fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma immune system disease intellectual disability juvenile pilocytic astrocytoma keratoconjunctivitis sicca learning disability leukemia lung cancer lung disease lung non-small cell carcinoma lung small cell carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma microcephaly mixed glioma mixed oligodendroglioma-astrocytoma myotonic dystrophy type 2 neurodegenerative disease neurofibroma neurofibromatosis 1 neurofibromatosis neurogenic arthropathy obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma partial motor epilepsy peripheral nervous system neoplasm pilocytic astrocytoma primary cutaneous T-cell non-Hodgkin lymphoma protoplasmic astrocytoma retinal vascular occlusion rheumatoid arthritis schizophrenia spinal cord disease subependymal giant cell astrocytoma syringomyelia systemic Epstein-Barr virus positive T-cell lymphoma of childhood tropical spastic paraparesis urinary bladder cancer visual epilepsy

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