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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 **651 - 675** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Aliases: Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	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 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
27232	glycine N-methyltransferase	GNMT	Homo sapiens (human)	glycine N-methyltransferase deficiency hepatocellular carcinoma
8443	glyceronephosphate O-acyltransferase	GNPAT Aliases: DAP-AT DAPAT DHAPAT dihydroxyacetone phosphate acyltransferase glycerone-phosphate O-acyltransferase	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 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
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 Aliases: GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin	Homo sapiens (human)
132789	glucosamine-6-phosphate deaminase 2	GNPDA2 Aliases: SB52 glucosamine-6-phosphate isomerase	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 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
64841	glucosamine-phosphate N-acetyltransferase 1	GNPNAT1 Aliases: FLJ10607 Gpnat1	Homo sapiens (human)	cancer diabetes mellitus diabetic ketoacidosis keratosis follicularis spinulosa decalvans type 2 diabetes mellitus
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB Aliases: KIAA1208 MGC4170	Homo sapiens (human)	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
84572	N-acetylglucosamine-1-phosphate transferase subunit gamma	GNPTG Aliases: CAB56184 GlcNAc-phosphotransferase gamma-subunit c316G12.3	Homo sapiens (human)	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis III gamma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
2799	glucosamine (N-acetyl)-6-sulfatase	GNS Aliases: N-acetylglucosamine-6-sulfatase Sanfilippo disease IIID	Homo sapiens (human)	brain cancer cancer diarrhea epilepsy fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability learning disability low tension glaucoma lysosomal storage disease melanoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis rheumatoid arthritis sensorineural hearing loss skin melanoma visual epilepsy
64083	golgi phosphoprotein 3	GOLPH3 Aliases: GOPP1 GPP34 MIDAS Vps74 coat-protein golgi peripheral membrane protein 1, 34 kDa golgi protein golgi-associated protein	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 Barrett's esophagus Glanzmann's thrombasthenia Hermansky-Pudlak syndrome 2 Japanese encephalitis Lyme disease Pick's disease Reye syndrome X-linked dyskeratosis congenita alternating hemiplegia of childhood anaplastic astrocytoma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anxiety disorder autonomic neuropathy bladder carcinoma blood coagulation disease breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer carcinoma catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system cancer central nervous system disease cerebral degeneration chikungunya childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer cholera chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation cystadenoma dengue disease dengue hemorrhagic fever depressive disorder dyskeratosis congenita dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension fibrillary astrocytoma fibromyalgia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma gray platelet syndrome hematopoietic system disease hepatitis A hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypochromic anemia hypohidrotic ectodermal dysplasia influenza juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma major depressive disorder malaria malignant astrocytoma melancholic depression melanoma microphthalmia migraine mixed glioma mucinous adenocarcinoma nervous system disease neuroblastoma neurotic disorder nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete inherited blood coagulation disease obsolete melancholia ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma papilloma phobic disorder pilocytic astrocytoma platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma qualitative platelet defect renal carcinoma renal cell carcinoma rhabdomyosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spinal stenosis squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tongue cancer urinary bladder cancer uterine corpus cancer viral infectious disease yellow fever
2805	glutamic-oxaloacetic transaminase 1	GOT1	Homo sapiens (human)	amyloidosis amyotrophic lateral sclerosis cardiomyopathy pancreatic ductal adenocarcinoma transient cerebral ischemia
2813	glycoprotein 2	GP2 Aliases: ZAP75	Homo sapiens (human)	Crohn's colitis Crohn's disease Ebola hemorrhagic fever acute myeloid leukemia classic galactosemia galactokinase deficiency galactosemia gallbladder disease gastroenteritis gastrointestinal system disease hepatitis C herpes zoster inflammatory bowel disease 1 inflammatory bowel disease intestinal disease liver disease microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma proctitis ulcerative colitis
8733	glycosylphosphatidylinositol anchor attachment 1	GPAA1 Aliases: GAA1 GPI transamidase subunit hGAA1	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 Cogan syndrome Friedreich ataxia 1 Friedreich ataxia Pick's disease Reye syndrome agnosia apraxia bladder carcinoma blindness breast cancer breast carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma congenital nystagmus diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy head and neck squamous cell carcinoma hepatocellular carcinoma intellectual disability large intestine cancer learning disability liver cancer liver cirrhosis myopia optic atrophy osteoporosis pathologic nystagmus spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma tongue squamous cell carcinoma urinary bladder cancer visual epilepsy
57678	glycerol-3-phosphate acyltransferase, mitochondrial	GPAM Aliases: GPAT1 KIAA1560 MGC26846 glycerol-3-phosphate acyltransferase 1, mitochondrial	Homo sapiens (human)	cancer embryoma familial nephrotic syndrome lipoid nephrosis melanoma metabolic dysfunction-associated steatotic liver disease nephrotic syndrome obesity overnutrition skin melanoma steatotic liver disease
150763	glycerol-3-phosphate acyltransferase 2, mitochondrial	GPAT2 Aliases: CT123 cancer/testis antigen 123	Homo sapiens (human)	adrenoleukodystrophy breast cancer breast carcinoma cancer melanoma skin melanoma
84803	glycerol-3-phosphate acyltransferase 3	GPAT3 Aliases: AGPAT10 HMFN0839 LPAAT-theta MAG1 MGC11324 lysophosphatidic acid acyltransferase, theta	Homo sapiens (human)	acquired immunodeficiency syndrome acute myeloid leukemia breast cancer cancer endometritis human immunodeficiency virus infectious disease leech infestation myiasis obesity toxoplasmosis
137964	glycerol-3-phosphate acyltransferase 4	GPAT4 Aliases: DKFZp586M1819 LPAAT-zeta TSARG7 lysophosphatidic acid acyltransferase, zeta	Homo sapiens (human)	diabetes mellitus type 2 diabetes mellitus
2817	glypican 1	GPC1 Aliases: glypican glypican proteoglycan 1	Homo sapiens (human)	Albright's hereditary osteodystrophy 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 Duchenne muscular dystrophy ITM2B-related cerebral amyloid angiopathy 1 ITM2B-related cerebral amyloid angiopathy 2 Kallmann syndrome Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Sheehan syndrome Simpson-Golabi-Behmel syndrome type 1 adenocarcinoma adenoma ameloblastoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma biliary atresia borderline personality disorder breast cancer breast carcinoma cancer central nervous system cancer cerebral amyloid angiopathy cerebral degeneration cervical cancer cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism craniosynostosis cribriform carcinoma embryoma epilepsy esophagus squamous cell carcinoma eyelid disease fibrodysplasia ossificans progressiva gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism intermittent explosive disorder intrahepatic cholangiocarcinoma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency large intestine cancer liver cancer lung adenocarcinoma lung cancer malignant epithelial mesothelioma malignant mesothelioma microphthalmia mixed glioma muscular dystrophy myositis ossificans myxedema nodular prostate obsolete Matthew-Wood syndrome ophthalmoplegia ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism placental insufficiency prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism pseudopseudohypoparathyroidism rheumatoid arthritis schizophrenia squamous cell carcinoma thymus gland disease tongue squamous cell carcinoma tubular adenocarcinoma visual epilepsy xanthomatosis
221914	glypican 2	GPC2 Aliases: DKFZp547M109 FLJ38962 cerebroglycan glypican proteoglycan 2, cerebroglycan proteoglycan	Homo sapiens (human)	breast cancer cancer embryoma hepatocellular carcinoma liver cancer neuroblastoma
2719	glypican 3	GPC3 Aliases: DGSX OCI-5 SGB SGBS SGBS1 glypican proteoglycan 3	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Crouzon syndrome Dandy-Walker syndrome Laron syndrome Marfan syndrome Meckel syndrome Meckel's diverticulum Perlman syndrome Proteus syndrome Simpson-Golabi-Behmel syndrome type 1 Sotos syndrome achondroplasia adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adult endodermal sinus tumor adult hepatocellular carcinoma adult medulloblastoma alcoholic liver cirrhosis ameloblastoma aniridia arthritis arthropathy 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 atypical teratoid rhabdoid tumor autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant polycystic kidney disease basal cell carcinoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer childhood hepatocellular carcinoma childhood medulloblastoma cholangiocarcinoma chondrosarcoma chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma cleft lip cleft palate clubfoot collecting duct carcinoma colorectal cancer colorectal carcinoma communicating hydrocephalus congenital diaphragmatic hernia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital mesoblastic nephroma craniosynostosis cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic kidney disease dextro-looped transposition of the great arteries distal arthrogryposis double outlet right ventricle early infantile epileptic encephalopathy embryoma embryonal cancer endodermal sinus tumor endometrial cancer endometrial carcinoma endometrial clear cell adenocarcinoma endomyocardial fibrosis epilepsy epithelioid sarcoma essential hypertension familial nephrotic syndrome follicular adenoma gallbladder cancer gallbladder carcinoma gallbladder disease germ cell and embryonal cancer germ cell cancer germinoma granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hidradenoma hydrocephalus hydronephrosis hypertension hypertrophic cardiomyopathy hypoglycemia immune system disease inguinal hernia intellectual disability intrahepatic cholangiocarcinoma isolated cleft palate large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy lipoid nephrosis liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microcystic adenoma mucinous adenocarcinoma multiple types of congenital heart defects 6 nephroblastoma nephrotic syndrome type 1 nephrotic syndrome neuroblastoma neuroendocrine carcinoma nevoid basal cell carcinoma syndrome non-congenital cyst of kidney nonpapillary renal cell carcinoma nonsyndromic congenital nail disorder 9 obsolete Opitz-GBBB syndrome obsolete dextro-looped transposition of the great arteries 1 obsolete mesoblastic nephroma obstructive hydrocephalus omphalocele osteoarthritis ovarian cancer ovarian carcinoma ovarian embryonal carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma patent ductus arteriosus patent foramen ovale placental insufficiency placental site trophoblastic tumor polydactyly polyhydramnios primary immunodeficiency disease prostate cancer prostate carcinoma renal agenesis renal carcinoma renal cell carcinoma rhabdoid cancer rhabdomyosarcoma salivary gland adenoid cystic carcinoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scoliosis sebaceous carcinoma seminoma senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag speech disorder spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma sweat gland cancer syringoma testicular cancer testicular germ cell cancer thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma umbilical hernia uterine corpus cancer ventricular septal defect viral infectious disease visual epilepsy
2262	glypican 5	GPC5 Aliases: glypican proteoglycan 5	Homo sapiens (human)	Balo concentric sclerosis Gilles de la Tourette syndrome MHC class II deficiency Marfan syndrome Simpson-Golabi-Behmel syndrome type 1 adenosine deaminase deficiency adrenoleukodystrophy bronchus cancer bronchus carcinoma cancer cardiac arrest cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types central nervous system cancer central nervous system disease central nervous system lymphoma demyelinating disease diabetes mellitus epithelioid sarcoma familial nephrotic syndrome gliosarcoma glomerulonephritis hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma microphthalmia mixed glioma multiple sclerosis myelomeningocele narcolepsy nephritis nephrotic syndrome neuromyelitis optica obsolete Matthew-Wood syndrome obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma proteinuria rhabdomyosarcoma rheumatoid arthritis sarcoma scoliosis severe combined immunodeficiency situs inversus spina bifida spindle cell sarcoma tethered spinal cord syndrome tetralogy of Fallot transthyretin amyloidosis tuberous sclerosis type 2 diabetes mellitus
10082	glypican 6	GPC6 Aliases: glypican proteoglycan 6	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 Simpson-Golabi-Behmel syndrome type 1 atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect attention deficit hyperactivity disorder blepharophimosis breast cancer breast carcinoma cancer cardiovascular system disease cavernous hemangioma cerebral degeneration chorioangioma colorectal cancer colorectal carcinoma craniosynostosis cryptorchidism degenerative disc disease dissociative disorder embryoma enterocele familial retinoblastoma glomus tumor heart disease hemangioma histiocytoid hemangioma intellectual disability intramuscular hemangioma large intestine cancer learning disability lymphangioma melanoma neurotic disorder omodysplasia 1 omodysplasia omphalocele osteoporosis ovarian cancer ovarian carcinoma patent foramen ovale pterygium reflex sympathetic dystrophy retinoblastoma schizophrenia skin melanoma trilateral retinoblastoma umbilical hernia ventricular septal defect
56261	glycerophosphocholine phosphodiesterase 1	GPCPD1 Aliases: GDE5 GDPD6 KIAA1434	Homo sapiens (human)	eating disorder endometrial cancer endometrial carcinoma obesity uterine corpus cancer
2819	glycerol-3-phosphate dehydrogenase 1	GPD1	Homo sapiens (human)	Laron syndrome Refsum disease Zellweger syndrome achondroplasia breast cancer breast carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma infantile Refsum disease inherited metabolic disorder liver cancer liver cirrhosis maturity-onset diabetes of the young mixed glioma obesity obstructive sleep apnea peroxisome biogenesis disorder 1A steatotic liver disease type 2 diabetes mellitus
23171	glycerol-3-phosphate dehydrogenase 1 like	GPD1L Aliases: KIAA0089	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome

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