GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **926 - 950** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB KIAA1208 MGC4170	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
64841	glucosamine-phosphate N-acetyltransferase 1	GNPNAT1 FLJ10607 Gpnat1	cancer diabetes mellitus diabetic ketoacidosis keratosis follicularis spinulosa decalvans type 2 diabetes mellitus
132789	glucosamine-6-phosphate deaminase 2	GNPDA2 SB52 glucosamine-6-phosphate isomerase	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 Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 allergic asthma asthma cardiovascular system disease cerebral degeneration diabetes mellitus essential hypertension heart disease hypertension intrinsic asthma obesity type 2 diabetes mellitus
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin
8443	glyceronephosphate O-acyltransferase	GNPAT DAP-AT DAPAT DHAPAT dihydroxyacetone phosphate acyltransferase glycerone-phosphate O-acyltransferase	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 Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata disease of mental health embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
27232	glycine N-methyltransferase	GNMT	glycine N-methyltransferase deficiency hepatocellular carcinoma
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	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 Bell's palsy GNE myopathy Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Paget's disease of bone Pick's disease Reye syndrome X-linked myopathy with excessive autophagy Zika fever amnestic disorder attention deficit hyperactivity disorder 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 cancer cardiomyopathy cerebral degeneration cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital central hypoventilation syndrome congenital hypothyroidism dementia distal myopathy endomyocardial fibrosis epilepsy esophagitis facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis frontotemporal dementia gastroesophageal reflux disease hypertrophic cardiomyopathy hypothyroidism inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myositis inguinal hernia intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myopathy myositis myxedema neuromuscular disease nonpapillary renal cell carcinoma 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 sleep apnea oculopharyngeal muscular dystrophy pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis sialuria sleep apnea thrombocytopenia tibial muscular dystrophy visual epilepsy
29925	GDP-mannose pyrophosphorylase B	GMPPB KIAA1851 mannose-1-phosphate guanyltransferase beta	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	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
2765	glycosylphosphatidylinositol anchored molecule like	GML LY6DL	acute lymphoblastic leukemia cancer cardiovascular system disease colorectal cancer colorectal carcinoma congenital adrenal hyperplasia embryoma esophageal cancer esophageal carcinoma essential hypertension giant cell glioblastoma glioblastoma glucocorticoid-remediable aldosteronism heart disease high grade glioma hypertension large intestine cancer lung cancer lung non-small cell carcinoma lymphoblastic lymphoma lymphoid leukemia myeloid leukemia
2762	GDP-mannose 4,6-dehydratase	GMDS GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	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
2760	ganglioside GM2 activator	GM2A GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3	Clostridium difficile colitis GM2 gangliosidosis, AB variant GM2 gangliosidosis Laron syndrome Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease achondroplasia alcohol dependence alcohol use disorder anxiety disorder blindness breast cancer breast carcinoma cancer cerebral degeneration choreatic disease chronic obstructive pulmonary disease dementia dystonia embryoma epilepsy generalized anxiety disorder neurodegenerative disease neuroendocrine carcinoma nicotine dependence perinatal necrotizing enterocolitis progressive muscular atrophy retinal disease retinitis spinal muscular atrophy syndromic X-linked intellectual disability type 10 visual epilepsy vulvovaginal candidiasis
132158	glycerate kinase	GLYCTK HBEBP2 HBEBP4	D-glyceric aciduria Unverricht-Lundborg syndrome blepharospasm brain disease early myoclonic encephalopathy epilepsy focal hand dystonia glycine encephalopathy intellectual disability lactic acidosis learning disability locked-in syndrome microcephaly obsolete infantile epileptic encephalopathy primary hyperoxaluria quadriplegia schizophrenia visual epilepsy
2752	glutamate-ammonia ligase	GLUL glutamine synthetase	Addison's disease Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Chagas disease Clostridium difficile colitis Graves' disease Griscelli syndrome type 2 Huntington's disease Lafora disease Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Stiff-Person syndrome Wernicke-Korsakoff syndrome Wilson disease acquired immunodeficiency syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adrenal cortical hypofunction adrenoleukodystrophy adult oligodendroglioma alcohol dependence alcohol use disorder alcoholic liver cirrhosis alternating hemiplegia of childhood amino acid metabolic disorder amnestic disorder amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy bacterial sepsis basal ganglia disease bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer brain disease brain stem infarction breast cancer breast carcinoma cancer cannabis abuse cannabis dependence carbamoyl phosphate synthetase I deficiency disease carcinoma cardiovascular system disease central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood oligodendroglioma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome complex partial epilepsy congenital hypothyroidism coronary artery disease dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma exanthem follicular adenoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hemochromatosis hepatic coma hepatic encephalopathy hepatoblastoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperglycemia hyperthyroidism hypothyroidism immune system disease intrahepatic cholangiocarcinoma iron metabolism disease irritable bowel syndrome lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression microcystic adenoma microphthalmia middle cerebral artery infarction mixed glioma mixed oligodendroglioma-astrocytoma molybdenum cofactor deficiency type A mood disorder movement disease myelitis myopia myxedema nervous system disease neurocirculatory asthenia neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 oligodendroglioma ornithine carbamoyltransferase deficiency osteosarcoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma papillary adenoma placental insufficiency primary open angle glaucoma progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder purpura retinal disease retinitis retrograde amnesia sarcoma sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma steatotic liver disease stomach cancer stomach carcinoma temporal lobe epilepsy thyrotoxicosis transient cerebral ischemia trypanosomiasis tuberculosis 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 urea cycle disorder visual epilepsy
51228	glycolipid transfer protein	GLTP	colon carcinoma colorectal cancer colorectal carcinoma hepatitis C large intestine cancer
83468	glycosyltransferase 8 domain containing 2	GLT8D2 FLJ31494	hepatitis C liver cirrhosis
55830	glycosyltransferase 8 domain containing 1	GLT8D1 AD-017 FLJ14611	amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy bipolar disorder depressive disorder dysplastic nevus syndrome dysthymic disorder generalized anxiety disorder laryngostenosis major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia osteoarthritis progressive muscular atrophy schizophrenia skin melanoma
360203	glycosyltransferase 6 domain containing 1	GLT6D1	acute pericementitis aggressive periodontitis periodontitis periodontosis
144423	glycosyltransferase 1 domain containing 1	GLT1D1 FLJ31978	St. Louis encephalitis allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis coronary artery disease intrinsic asthma
2739	glyoxalase I	GLO1 GLOD1 lactoylglutathione lyase	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 Graves' disease 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 Miller Fisher syndrome Pick's disease Reye syndrome Sjogren's syndrome Werner syndrome acute myocardial infarction adult fibrosarcoma anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia bipolar disorder bladder carcinoma bone disease breast cancer breast carcinoma cancer carcinoma carotid artery disease cartilage disease central nervous system cancer cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebrovascular disease clear cell adenocarcinoma clear cell renal cell carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital adrenal hyperplasia connective tissue disease coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dysthymic disorder embryoma end stage renal disease endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma essential hypertension familial mediterranean fever familial nephrotic syndrome fibrosarcoma fundus albipunctatus gallbladder disease generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperthyroidism inflammatory breast carcinoma keratoconjunctivitis sicca kidney cancer kidney disease large intestine cancer lipoid nephrosis liver cancer liver cirrhosis liver disease major depressive disorder malaria melancholic depression melanoma mevalonic aciduria mixed glioma mood disorder motor neuritis multiple myeloma multiple sclerosis myocardial infarction nephritis nephrosis nephrotic syndrome neuritis neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis pancreatic cancer pancreatic carcinoma panic disorder phobic disorder progeria prostate cancer prostate carcinoma pyoureter renal carcinoma renal cell carcinoma restless legs syndrome retinal disease retinitis pigmentosa retinitis sarcomatoid carcinoma schizophrenia silent myocardial infarction skin melanoma spinocerebellar ataxia type 1 stomach cancer stomach carcinoma subacute sclerosing panencephalitis synovial sarcoma systemic lupus erythematosus thyroid gland anaplastic carcinoma thyrotoxicosis 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 urinary bladder cancer uterine corpus cancer vascular disease visual epilepsy
256710	GLIPR1 like 1	GLIPR1L1 MGC26856
2731	glycine decarboxylase	GLDC GCSP NKH glycine cleavage system protein P glycine dehydrogenase nonketotic hyperglycinemia	B-cell lymphoma Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Marfan syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome allergic asthma asthma autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal ganglia disease blepharospasm bone osteosarcoma brain disease bronchus cancer bronchus carcinoma cancer central nervous system cancer chondrodysplasia-pseudohermaphroditism syndrome chromosome 9p deletion syndrome communicating hydrocephalus conduct disorder disease of metabolism early myoclonic encephalopathy embryoma epilepsy focal hand dystonia frontotemporal dementia gliosarcoma glycine encephalopathy hepatocellular carcinoma high grade glioma hydrocephalus hyperglycemia idiopathic generalized epilepsy influenza intellectual disability intrinsic asthma large cell carcinoma learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mixed glioma neuroblastoma obesity obsolete ymphosarcoma obstructive hydrocephalus osteosarcoma progressive supranuclear palsy prostate cancer prostate carcinoma red-green color blindness schizophrenia senile degeneration of brain situs inversus stomach cancer stomach carcinoma tuberous sclerosis viral infectious disease visual epilepsy
26035	glucuronic acid epimerase	GLCE HSEPI KIAA0836 heparan sulfate epimerase	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions amyotrophic lateral sclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebrovascular disease embryoma essential hypertension frontotemporal dementia hypertension luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma nodular prostate progressive muscular atrophy prostate cancer prostate carcinoma prostate disease prostatic adenoma
112937	galactosidase beta 1 like 3	GLB1L3 FLJ90231
89944	galactosidase beta 1 like 2	GLB1L2	acute myeloid leukemia

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