GlyCosmos Portal

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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 **392651 - 392675** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
10747	MBL associated serine protease 2	MASP2 Aliases: MAP-2 Map19 mannose-binding lectin associated protein 19 mannose-binding lectin-associated serine protease 2 sMAP	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Chagas disease Crohn's colitis Crohn's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Kuhnt-Junius degeneration Langerhans-cell histiocytosis Stevens-Johnson syndrome Streptococcus pneumonia angioedema autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis cancer cardiac arrest cardiomyopathy cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chronic fatigue syndrome colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency cystic fibrosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma embryoma encephalomyelitis endomyocardial fibrosis erythema multiforme esophagus squamous cell carcinoma follicular lymphoma frontotemporal dementia glomerulonephritis hepatitis C hepatocellular carcinoma hereditary angioedema hypersensitivity reaction type III disease hypertrophic cardiomyopathy immune system disease inflammatory bowel disease 1 inflammatory bowel disease kidney disease large intestine cancer lepromatous leprosy leprosy liver cancer lymphoma malaria multiple sclerosis nephritis nephrosis non-Hodgkin lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ovarian cancer ovarian carcinoma parapsoriasis pneumonia psoriasis pustulosis of palm and sole pyoureter reticulosarcoma rheumatic fever rheumatoid arthritis sarcoidosis severe acute respiratory syndrome sporotrichosis systemic lupus erythematosus trypanosomiasis tuberculosis 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 type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis urinary schistosomiasis viral infectious disease
10728	prostaglandin E synthase 3	PTGES3 Aliases: TEBP cPGES p23	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Lyme disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adult fibrosarcoma alexia aortic valve insufficiency atherosclerosis autism spectrum disorder autistic disorder bone osteosarcoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration childhood acute lymphocytic leukemia childhood osteosarcoma cribriform carcinoma cryptosporidiosis cystic fibrosis diarrhea dyslexia embryoma esophageal cancer esophageal carcinoma familial retinoblastoma fibrosarcoma granular cell carcinoma hepatitis C intrahepatic cholestasis of pregnancy lung adenocarcinoma lung cancer lung non-small cell carcinoma neurodegenerative disease oligodendroglioma osteosarcoma papillary adenocarcinoma papillary renal cell carcinoma periodontitis prostate cancer prostate carcinoma retinoblastoma sarcomatoid carcinoma schizophrenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma toxic encephalopathy trilateral retinoblastoma tubular adenocarcinoma
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 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 type 2 diabetes mellitus visual epilepsy
10720	UDP glucuronosyltransferase family 2 member B11	UGT2B11	Homo sapiens (human)	cholangiocarcinoma intrahepatic cholangiocarcinoma prostate cancer prostate carcinoma
10715	ceramide synthase 1	CERS1 Aliases: LAG1 UOG1	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis blepharospasm cancer central nervous system cancer congestive heart failure coronary artery disease dementia dengue disease dentatorubral-pallidoluysian atrophy double outlet right ventricle early myoclonic encephalopathy embryoma focal hand dystonia gliosarcoma hand, foot and mouth disease head and neck squamous cell carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability learning disability malaria mixed glioma multiple types of congenital heart defects 6 neuroblastoma papillary adenocarcinoma papillary renal cell carcinoma primary spontaneous pneumothorax progressive myoclonus epilepsy 4 progressive myoclonus epilepsy 8 progressive myoclonus epilepsy steatotic liver disease tetralogy of Fallot thyroid gland papillary carcinoma ulcerative colitis viral infectious disease visceral heterotaxy visual epilepsy yellow fever
10690	fucosyltransferase 9	FUT9 Aliases: Fuc-TIX alpha (1,3) fucosyltransferase	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer candidiasis colorectal cancer colorectal carcinoma embryoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma malaria
10682	EBP cholestenol delta-isomerase	EBP Aliases: 3-beta-hydroxysteroid-delta-8,delta-7-isomerase CHO2 CPX CPXD Chondrodysplasia punctata-2, X-linked dominant (Happle syndrome) sterol 8-isomerase	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Dandy-Walker syndrome Klinefelter syndrome Klippel-Feil syndrome Krabbe disease Laron syndrome MEND syndrome Marfan syndrome Patau syndrome Peters anomaly Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked cleft palate with or without ankyloglossia achondroplasia actinic keratosis acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adrenoleukodystrophy adult fibrosarcoma allergic asthma alopecia ankyloglossia aortic valve disease 2 aortic valve stenosis arteriosclerotic cardiovascular disease asthma atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cartilage-hair hypoplasia cataract central nervous system cancer central nervous system disease cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute myeloid leukemia childhood leukemia chondrodysplasia punctata choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma cleft palate clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congenital heart disease congenital nystagmus congenital ptosis congestive heart failure cornea plana coronary artery disease cryptorchidism cystic fibrosis dementia diabetes mellitus dissociated nystagmus embryoma epilepsy essential hypertension essential thrombocythemia familial retinoblastoma fibrosarcoma gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gliosarcoma granuloma annulare hematologic cancer hemophilia B hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hydrocephalus hydronephrosis hyperostosis hypertension ichthyosis intellectual disability intrinsic asthma isolated cleft palate keratosis follicularis kidney failure large intestine cancer laryngeal disease learning disability leiomyoma leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma microphthalmia mixed glioma mixed-type liposarcoma mongolian spot mucopolysaccharidosis IV multicentric Castleman disease multiple epiphyseal dysplasia myelodysplastic syndrome myeloid leukemia myofibroma myxoid liposarcoma narcolepsy nervous system disease neuroblastoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete congenital ichthyosiform erythroderma obstructive hydrocephalus optic atrophy osteochondrodysplasia osteomyelitis papillary adenocarcinoma papillary renal cell carcinoma papilloma pathologic nystagmus placenta cancer polydactyly polyhydramnios pseudoxanthoma elasticum ptosis renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcomatoid renal cell carcinoma schizophrenia scoliosis seborrheic keratosis senile degeneration of brain sensorineural hearing loss situs inversus skin disease skin melanoma spondylolisthesis spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal calcification tracheal disease tracheal stenosis trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy
10678	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 Aliases: B3GN-T1 B3GN-T2 B3GNT-2 BETA3GNT	Homo sapiens (human)	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
10675	chondroitin sulfate proteoglycan 5	CSPG5 Aliases: NGC neuroglycan C	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Japanese encephalitis Perlman syndrome Sotos syndrome dengue disease schizophrenia viral infectious disease yellow fever
10610	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	ST6GALNAC2 Aliases: ST6GalNAII STHM	Homo sapiens (human)	IgA glomerulonephritis breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma depressive disorder embryoma large intestine cancer major depressive disorder melancholic depression melanoma obsolete melancholia skin melanoma thyroid gland follicular carcinoma
10591	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	DNPH1 Aliases: dJ330M21.3 rcl	Homo sapiens (human)
10585	protein O-mannosyltransferase 1	POMT1 Aliases: LGMD2K dolichyl-phosphate-mannose-protein mannosyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome 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 bilateral optic nerve hypoplasia blindness brain cancer brain disease buphthalmos campomelic dysplasia cardiomyopathy cataract centronuclear myopathy cleft lip cleft palate clubfoot coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy 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-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus albipunctatus fundus dystrophy glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly locked-in syndrome mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis nemaline myopathy neuromuscular disease 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy peripheral retinal degeneration placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 quadriplegia recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
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
10559	solute carrier family 35 member A1	SLC35A1 Aliases: CMP-Sia-Tr CMP-sialic acid transporter CMPST hCST	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia 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 type 2 diabetes mellitus ulcerative colitis viral infectious disease visual epilepsy
10558	serine palmitoyltransferase long chain base subunit 1	SPTLC1 Aliases: HSAN1 LCB1 SPTI hLCB1	Homo sapiens (human)	Alzheimer's disease 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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Riley-Day syndrome acquired hyperkeratosis agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood autonomic neuropathy bipolar disorder brain cancer breast cancer cancer central nervous system cancer central nervous system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma dementia diabetes mellitus disease of mental health embryoma frontotemporal dementia gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 2 hereditary sensory and autonomic neuropathy type 5 hereditary sensory neuropathy type 4 hereditary sensory neuropathy high grade glioma juvenile amyotrophic lateral sclerosis type 27 keratosis mixed glioma motor peripheral neuropathy nervous system disease neurodegenerative disease neuropathy nonpapillary renal cell carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum papillary renal cell carcinoma peripheral nervous system disease polyneuropathy psychotic disorder renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss sensory peripheral neuropathy skin disease type 2 diabetes mellitus
10555	1-acylglycerol-3-phosphate O-acyltransferase 2	AGPAT2 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase beta LPAAT-beta LPLAT2 lysophosphatidic acid acyltransferase-beta lysophospholipid acyltransferase 2	Homo sapiens (human)	Fanconi syndrome Zollinger-Ellison syndrome acanthosis nigricans acute myocardial infarction acute pancreatitis acute promyelocytic leukemia aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atrichia with papular lesions bone osteosarcoma bulimia nervosa cancer cardiomyopathy childhood osteosarcoma chronic myeloid leukemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congestive heart failure coronary artery disease coronary thrombosis cystinosis diabetes mellitus diabetic ketoacidosis embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis familial hypertrophic cardiomyopathy familial partial lipodystrophy familial periodic paralysis glomerulonephritis hydrocephalus hyperinsulinism hypertrichosis hypertrophic cardiomyopathy intellectual disability isolated growth hormone deficiency kidney disease kidney failure learning disability lipoatrophic diabetes mellitus lipodystrophy myocardial infarction myopathy neonatal diabetes nephritis nephrolithiasis nephrosis neuropathy obesity omphalocele osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatitis peripheral nervous system disease polycystic ovary syndrome primary immunodeficiency disease primary pulmonary hypertension pyloric stenosis pyoureter scoliosis silent myocardial infarction steatotic liver disease transient neonatal diabetes mellitus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome type 2 diabetes mellitus umbilical hernia uric acid nephrolithiasis uterine corpus cancer
10554	1-acylglycerol-3-phosphate O-acyltransferase 1	AGPAT1 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase alpha LPAAT-alpha LPLAT1 lysophosphatidic acid acyltransferase, alpha lysophospholipid acyltransferase l	Homo sapiens (human)	Japanese encephalitis cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dengue disease diabetic ketoacidosis embryoma lipoatrophic diabetes mellitus lipodystrophy obsolete type 1 diabetes mellitus 9 pancreatic cancer pancreatic carcinoma rheumatoid arthritis steatotic liver disease 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 viral infectious disease yellow fever
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
10462	C-type lectin domain containing 10A	CLEC10A Aliases: CD301 HML HML2 macrophage lectin 2 (calcium dependent)	Homo sapiens (human)	B-cell lymphoma Crohn's colitis Crohn's disease Ebola hemorrhagic fever acquired immunodeficiency syndrome acrodermatitis adenosquamous carcinoma adult lymphoma allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease asthma atopic dermatitis autosomal recessive distal hereditary motor neuronopathy 1 bipolar disorder breast cancer breast carcinoma cancer celiac disease central nervous system lymphoma centronuclear myopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood lymphoma cholesteatoma cholinergic urticaria congenital structural myopathy coronary artery disease dermatitis embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypereosinophilic syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma lateral sclerosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma melanoma motor neuron disease neurodegenerative disease obsolete malignant histiocytosis obsolete ymphosarcoma ovarian cancer ovarian carcinoma peripheral T-cell lymphoma polyp of middle ear progressive muscular atrophy prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia skin melanoma squamous cell carcinoma teratocarcinoma tongue squamous cell carcinoma transient myeloproliferative syndrome tubular aggregate myopathy 1 ulcerative colitis viral infectious disease
10457	glycoprotein nmb	GPNMB Aliases: HGFIN NMB glycoprotein NMB glycoprotein nmb-like protein glycoprotein nonmetastatic melanoma protein B hematopoietic growth factor inducible neurokinin-1 osteoactivin transmembrane glycoprotein	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 Gaucher's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sveinsson chorioretinal atrophy acute kidney failure acute myocardial infarction adenocarcinoma adenoma adult liposarcoma amyloidosis amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy bladder carcinoma bone disease bone osteosarcoma brain cancer brain infarction brain ischemia breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood liposarcoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma connective tissue disease coronary thrombosis cystic fibrosis distal arthrogryposis embryoma endometriosis of uterus endometriosis follicular adenoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liposarcoma liver cancer liver cirrhosis lymphangioleiomyomatosis lysosomal storage disease melanoma microcystic adenoma microphthalmia mixed glioma monoclonal gammopathy of uncertain significance myocardial infarction neurodegenerative disease nonpapillary renal cell carcinoma open-angle glaucoma osteoarthritis osteoporosis osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma periodontal disease phobic disorder pigment dispersion syndrome pleomorphic liposarcoma primary localized cutaneous amyloidosis 3 progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma ureteral obstruction urinary bladder cancer
10455	enoyl-CoA delta isomerase 2	ECI2 Aliases: ACBD2 DRS1 HCA88 Hepatocellular carcinoma-associated antigen 88 acyl-Coenzyme A binding domain containing 2	Homo sapiens (human)	aplastic anemia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma pure red-cell aplasia
10449	acetyl-CoA acyltransferase 2	ACAA2 Aliases: DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
10434	lysophospholipase 1	LYPLA1 Aliases: APT-1 LPL1 acyl-protein thioesterase 1	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome cancer carcinoma diabetes mellitus embryoma lung cancer lung non-small cell carcinoma melanoma pancreatic cancer prostate cancer prostate carcinoma sarcomatoid carcinoma skin melanoma type 2 diabetes mellitus
10423	CDP-diacylglycerol--inositol 3-phosphatidyltransferase	CDIPT Aliases: PIS PIS1 phosphatidylinositol synthase	Homo sapiens (human)	cancer disorder of sexual development hermaphroditism myasthenia gravis pseudohermaphroditism steatotic liver disease
10402	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	ST3GAL6 Aliases: ST3GALVI	Homo sapiens (human)	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer

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