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 **1426 - 1450** of **1582** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
29925	GDP-mannose pyrophosphorylase B	GMPPB Aliases: KIAA1851 mannose-1-phosphate guanyltransferase beta	Homo sapiens (human)	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia 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 cardiomyopathy cataract centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B14 muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia 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 pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
29926	GDP-mannose pyrophosphorylase A	GMPPA	Homo sapiens (human)	Addison's disease Down syndrome Laron syndrome achalasia achondroplasia adrenal cortical hypofunction alacrima, achalasia, and impaired intellectual development syndrome blindness coloboma epilepsy intellectual disability learning disability megaesophagus microcephaly nonepidermolytic palmoplantar keratoderma optic atrophy palmoplantar keratosis sensorineural hearing loss triple-A syndrome visual epilepsy
2762	GDP-mannose 4,6-dehydratase	GMDS Aliases: GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	Homo sapiens (human)	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IIc embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
390637	GDP-D-glucose phosphorylase 1	GDPGP1	Homo sapiens (human)
64096	GDNF family receptor alpha 4	GFRA4 Aliases: persephin receptor	Homo sapiens (human)	Hirschsprung's disease allergic asthma asthma intrinsic asthma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A panic disorder
2675	GDNF family receptor alpha 2	GFRA2 Aliases: GDNFRB NTNRA RETL2 TRNR2	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Parkinsonism adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
2674	GDNF family receptor alpha 1	GFRA1 Aliases: GDNFR GFR-ALPHA-1 RET1L RETL1 TRNR1	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 Churg-Strauss syndrome Hirschsprung's disease Kennedy's disease Parkinsonism Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyarteritis nodosa polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma renal agenesis rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
2215	Fc gamma receptor IIIb	FCGR3B Aliases: CD16 CD16b FcRIIIb FcgammaRIIIb	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 Behcet's disease Burkitt lymphoma CINCA Syndrome CREST syndrome Crohn's colitis Crohn's disease Down syndrome Evans' syndrome Gaucher's disease Goodpasture syndrome Graves' disease Griscelli syndrome Guillain-Barre syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis Lown-Ganong-Levine syndrome Marfan syndrome Meniere's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis Wolff-Parkinson-White syndrome X-linked agammaglobulinemia Zika fever Zollinger-Ellison syndrome abdominal aortic aneurysm acoustic neuroma acquired immunodeficiency syndrome acute chest syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute pericementitis adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult lymphoma age related macular degeneration aggressive NK-cell leukemia aggressive periodontitis agnosia agranulocytosis allergic asthma allergic contact dermatitis amyotrophic lateral sclerosis anemia angioedema angiomatous meningioma ankylosing spondylitis aortic valve disease 2 aortic valve stenosis aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant familial periodic fever bacterial sepsis benign meningioma bile duct adenocarcinoma bile duct carcinoma biliary atresia breast cancer breast carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease carotid artery thrombosis carotid stenosis cataract 32 multiple types central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma cholangiocarcinoma chordoma chromophobe renal cell carcinoma chronic NK-cell lymphocytosis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency congenital hypogammaglobulinemia coronary artery disease coronary thrombosis crescentic glomerulonephritis cribriform carcinoma cryoglobulinemia cryptococcosis cystic fibrosis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever denture stomatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma distal arthrogryposis eczema herpeticum embryoma endolymphatic hydrops endometriosis of uterus endometriosis epidermodysplasia verruciformis epithelioid leiomyosarcoma epithelioid sarcoma essential thrombocythemia familial hyperlipidemia familial nephrotic syndrome fetal erythroblastosis fibrous meningioma gastritis glomerulonephritis glucose intolerance glycogen storage disease II granular cell carcinoma granulomatosis with polyangiitis head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypersensitivity vasculitis hyperthyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile myelomonocytic leukemia kidney disease kidney failure kwashiorkor large intestine cancer leiomyosarcoma leukemia leukopenia lipoid nephrosis liver cancer liver cirrhosis lung cancer lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macrocytic anemia macular degeneration malaria marasmus melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia multiple myeloma multiple sclerosis myelodysplastic syndrome myeloproliferative disorder with eosinophilia myocardial infarction myxoid leiomyosarcoma nephritis nephrotic syndrome type 2 nephrotic syndrome neuroblastoma neutropenia non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsessive-compulsive disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete malignant histiocytosis obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma olfactory groove meningioma oophoritis osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parametritis parapsoriasis parasagittal meningioma paroxysmal nocturnal hemoglobinuria pelvic inflammatory disease periodontal disease periodontitis periodontosis phototoxic dermatitis pituitary adenoma pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis prediabetes syndrome progressive muscular atrophy protein-energy malnutrition psammomatous meningioma psoriasis psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole pyosalpinx rapidly progressive glomerulonephritis red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease reticulosarcoma rheumatic fever rheumatoid arthritis salpingitis sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma secretory meningioma severe congenital neutropenia sickle cell anemia silent myocardial infarction situs inversus skin disease skin melanoma speech-language disorder-1 spinal meningioma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma steatotic liver disease stomatitis subacute delirium systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma temporal arteritis thrombocytopenia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma toxic shock syndrome transient hypogammaglobulinemia of infancy transitional meningioma tuberculosis tuberculous pneumothorax tuberous sclerosis tubular adenocarcinoma 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 uremia urticaria uveoparotid fever vascular disease vasculitis viral infectious disease yellow fever
2208	Fc epsilon receptor II	FCER2 Aliases: C-type lectin domain family 4 member J CD23 CLEC4J FCErII Fc epsilon RII FcepsilonRII	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma CD40 ligand deficiency Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kawasaki disease Langerhans cell sarcoma Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Wiskott-Aldrich syndrome X-linked agammaglobulinemia X-linked hyper IgM syndrome acquired immunodeficiency syndrome acute myeloid leukemia adult lymphoma agammaglobulinemia aggressive systemic mastocytosis allergic asthma asthma atopic dermatitis 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 recessive congenital ichthyosis 4B cancer central nervous system lymphoma childhood T-cell acute lymphoblastic leukemia childhood leukemia childhood lymphoma chronic eosinophilic leukemia chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia chronic monocytic leukemia clonorchiasis congenital hypogammaglobulinemia dermatitis diabetic ketoacidosis encephalitis encephalomyelitis enterobiasis extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue follicular dendritic cell sarcoma follicular lymphoma food allergy gastric lymphoma gastritis human immunodeficiency virus infectious disease hyper IgM syndrome hyperthyroidism immunodeficiency with hyper IgM type 3 indolent systemic mastocytosis inflammatory bowel disease interdigitating dendritic cell sarcoma interstitial lung disease intestinal schistosomiasis intrinsic asthma leukemia lymphoid leukemia lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma mastocytosis mediastinal gray zone lymphoma multiple myeloma myelitis myeloid leukemia nasopharynx carcinoma obsolete congenital ichthyosiform erythroderma obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma parasitic helminthiasis infectious disease primary mediastinal B-cell lymphoma primary polycythemia prolymphocytic leukemia rheumatoid arthritis schistosomiasis severe acute respiratory syndrome squamous cell carcinoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic mastocytosis thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma trichinosis 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
158326	FRAS1 related extracellular matrix 1	FREM1 Aliases: C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	Homo sapiens (human)	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
9896	FIG4 phosphoinositide 5-phosphatase	FIG4 Aliases: ALS11 CMT4J SAC3 dJ249I4.1 hSac3	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 3 Charcot-Marie-Tooth disease type 4 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 Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Papillon-Lefevre disease Yunis-Varon syndrome achondroplasia agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease anxiety disorder 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 autosomal recessive distal hereditary motor neuronopathy 1 bilateral parasagittal parieto-occipital polymicrogyria breast cancer breast carcinoma cardiomyopathy cataract communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cryptorchidism demyelinating disease demyelinating polyneuropathy depressive disorder distal arthrogryposis dysthymic disorder endomyocardial fibrosis enophthalmos epilepsy essential hypertension generalized anxiety disorder gingival recession gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 7 high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertension hypertrophic cardiomyopathy hypospadias laryngostenosis lateral sclerosis lissencephaly lysosomal storage disease major depressive disorder melancholic depression microcephaly mixed glioma motor neuron disease motor peripheral neuropathy neuroblastoma neurodegenerative disease neuropathy neurotic disorder obsolete exophthalmos obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive hydrocephalus orbital disease patent foramen ovale peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary pulmonary hypertension progressive muscular atrophy pyloric stenosis renal artery obstruction renovascular hypertension sclerocornea senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus status epilepticus subacute delirium syndactyly syndromic X-linked intellectual disability Najm type tetralogy of Fallot tuberous sclerosis ventricular septal defect
55277	FGGY carbohydrate kinase domain containing	FGGY	Homo sapiens (human)
9917	FAM20B glycosaminoglycan xylosylkinase	FAM20B Aliases: GXK1 KIAA0475	Homo sapiens (human)	Desbuquois dysplasia Ehlers-Danlos syndrome osteogenesis imperfecta parapsoriasis psoriasis pustulosis of palm and sole
93611	F-box protein 44	FBXO44 Aliases: FBG3 FBX30 Fbx44 Fbxo6a MGC14140	Homo sapiens (human)	polycystic ovary syndrome prostate cancer prostate carcinoma
26232	F-box protein 2	FBXO2 Aliases: FBX2 Fbg1 Fbs1 Nfb42	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome cerebral degeneration hyperglycemia rheumatoid arthritis stomach cancer stomach carcinoma
115290	F-box protein 17	FBXO17 Aliases: F-box only protein 26 FBG4 FLJ11798 FLJ25205 Fbx17 MGC9379	Homo sapiens (human)	cancer embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma
54206	ERBB receptor feedback inhibitor 1	ERRFI1	Homo sapiens (human)	endometrial cancer osteoarthritis
80267	ER degradation enhancing alpha-mannosidase like protein 3	EDEM3	Homo sapiens (human)	congenital disorder of glycosylation type II hepatitis C prostate cancer prostate carcinoma
55741	ER degradation enhancing alpha-mannosidase like protein 2	EDEM2 Aliases: FLJ10783 bA4204.1	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 cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid
9695	ER degradation enhancing alpha-mannosidase like protein 1	EDEM1 Aliases: EDEM KIAA0212	Homo sapiens (human)	cystic fibrosis depressive disorder hepatitis C major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia skin melanoma
9852	EPM2A interacting protein 1	EPM2AIP1	Homo sapiens (human)
7957	EPM2A glucan phosphatase, laforin	EPM2A Aliases: LD LDE	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Dravet syndrome Lafora disease MERRF syndrome Rett syndrome Unverricht-Lundborg syndrome adrenoleukodystrophy adult lymphoma agnosia alexia apraxia benign epilepsy with centrotemporal spikes blepharospasm blindness cancer central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma cystinuria dementia dentatorubral-pallidoluysian atrophy depressive disorder dyslexia dysthymic disorder early myoclonic encephalopathy embryoma endometrial carcinoma epilepsy focal hand dystonia galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease intellectual disability learning disability lymphoma major depressive disorder melancholic depression narcolepsy neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder non-syndromic X-linked intellectual disability obsolete Dravet syndrome obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma photosensitive epilepsy photosensitivity disease progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder status epilepticus
79993	ELOVL fatty acid elongase 7	ELOVL7 Aliases: FLJ23563	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy cancer hidradenitis suppurativa hidradenitis inflammatory bowel disease multiple system atrophy pompholyx prostate cancer prostate carcinoma
79071	ELOVL fatty acid elongase 6	ELOVL6 Aliases: FLJ23378 LCE MGC5487	Homo sapiens (human)	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
60481	ELOVL fatty acid elongase 5	ELOVL5 Aliases: HELO1 dJ483K16.1	Homo sapiens (human)	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus

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