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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	October 29, 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 **6801 - 6825** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
51301	glucosaminyl (N-acetyl) transferase 4	GCNT4 Aliases: C2GNT3 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 core 2 beta-1,6-N-acetylglucosaminyltransferase 3	Homo sapiens (human)
9245	glucosaminyl (N-acetyl) transferase 3, mucin type	GCNT3 Aliases: C2/4GnT C2GnT-M C2GnT2	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma hepatocellular carcinoma large intestine cancer liver cancer lung cancer lung non-small cell carcinoma melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma
2651	glucosaminyl (N-acetyl) transferase 2 (I blood group)	GCNT2 Aliases: IGNT Ii blood group NAGCT1 ULG3 bA360O19.2 bA421M1.1 unassigned linkage group 3	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cancer 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 cataract cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma esophagus squamous cell carcinoma gallbladder cancer gallbladder carcinoma hyperferritinemia-cataract syndrome kidney failure large intestine cancer melanoma skin melanoma tuberculosis uremia
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)	adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma embryoma granular cell carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma neuroblastoma pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma seminoma testicular cancer testicular germ cell cancer tubular adenocarcinoma
93953	germ cell nuclear acidic peptidase	GCNA	Homo sapiens (human)
10985	GCN1 activator of EIF2AK4	GCN1	Homo sapiens (human)
8521	glial cells missing transcription factor 1	GCM1	Homo sapiens (human)
2729	glutamate-cysteine ligase catalytic subunit	GCLC	Homo sapiens (human)	cataract colorectal cancer cystic fibrosis glutamate-cysteine ligase deficiency hemolytic anemia liver cirrhosis myocardial infarction pulmonary emphysema
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis 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 visceral leishmaniasis visual epilepsy
2642	glucagon receptor	GCGR	Homo sapiens (human)
2641	glucagon	GCG	Homo sapiens (human)	Alzheimer's disease prediabetes syndrome
2639	glutaryl-CoA dehydrogenase	GCDH Aliases: ACAD5 GCD	Homo sapiens (human)	D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria Fleck corneal dystrophy alternating hemiplegia of childhood autonomic neuropathy basal ganglia disease blepharospasm brain disease brain ischemia central nervous system disease central nervous system origin vertigo cerebral palsy colorectal cancer colorectal carcinoma corneal dystrophy disease of metabolism dystonia epilepsy focal hand dystonia generalized dystonia glutaric acidemia I granular corneal dystrophy 2 hemiplegia hyperlysinemia hypoglycemia inherited metabolic disorder lactic acidosis large intestine cancer lattice corneal dystrophy lingual-facial-buccal dyskinesia liver cirrhosis malignant hyperthermia migraine movement disease nervous system disease oligohydramnios spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy speech disorder transient cerebral ischemia visual epilepsy
9648	GRIP and coiled-coil domain containing 2	GCC2	Homo sapiens (human)
2638	GC vitamin D binding protein	GC	Homo sapiens (human)
115362	guanylate binding protein 5	GBP5	Homo sapiens (human)
115361	guanylate binding protein 4	GBP4 Aliases: Mpa2	Homo sapiens (human)
26301	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)	GBGT1 Aliases: A3GALNT FS Forssman blood group Forssman glycolipid synthetase (FS) Forssman synthetase MGC44848 UDP-GalNAc	Homo sapiens (human)	cancer celiac disease embryoma ovarian cancer ovarian carcinoma thrombophilia
8729	golgi brefeldin A resistant guanine nucleotide exchange factor 1	GBF1	Homo sapiens (human)
2632	1,4-alpha-glucan branching enzyme 1	GBE1 Aliases: Andersen disease glycogen branching enzyme glycogen storage disease type IV	Homo sapiens (human)	B-cell lymphoma Cauda equina syndrome Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Guillain-Barre syndrome Noonan syndrome 1 acute myeloid leukemia bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic ulcer of skin chylomicron retention disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome cystinuria cytochrome-c oxidase deficiency disease dementia diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial lipoprotein lipase deficiency familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy idiopathic scoliosis intellectual disability learning disability leukodystrophy lipid storage disease liver disease locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy melanoma mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy neurogenic bladder obsolete ymphosarcoma ovarian cancer ovarian carcinoma paraplegia polyhydramnios porphyria portal hypertension pulmonary tuberculosis quadriplegia rigid spine muscular dystrophy 1 skin melanoma
57733	glucosylceramidase beta 3 (gene/pseudogene)	GBA3 Aliases: CBGL1 GLUC KLrP cytosolic β-glucosidase-like protein-1 klotho-related protein	Homo sapiens (human)	Gaucher's disease type I Gaucher's disease Goodpasture syndrome Takayasu's arteritis West Nile fever allergic asthma asthma cancer cystic fibrosis diabetic ketoacidosis granulomatosis with polyangiitis hepatocellular carcinoma kidney disease liver cancer obsolete type 1 diabetes mellitus 9 polyarteritis nodosa stomach cancer stomach carcinoma substance abuse substance-related disorder 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
57704	glucosylceramidase beta 2	GBA2 Aliases: AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
2629	glucosylceramidase beta 1	GBA1 Aliases: glucocerebrosidase	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 Burkitt lymphoma Canavan disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Cogan syndrome DiGeorge syndrome Fabry disease Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Lafora disease Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Netherton syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Niemann-Pick disease PCWH syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease REM sleep behavior disorder Reye syndrome Sjogren-Larsson syndrome Tay-Sachs disease Unverricht-Lundborg syndrome West Nile fever Wolman disease abdominal obesity-metabolic syndrome 1 achondroplasia acquired hyperkeratosis actinic keratosis adult lymphoma agenesis of the corpus callosum with peripheral neuropathy agnosia alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy atypical Gaucher's disease due to saposin c deficiency autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis autosomal recessive osteopetrosis 7 blepharospasm brain disease cancer cardiac arrest central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma chylomicron retention disease communicating hydrocephalus congestive heart failure dementia dentatorubral-pallidoluysian atrophy depressive disorder developmental coordination disorder diffuse interstitial keratitis diffuse large B-cell lymphoma dissociated nystagmus dysthymic disorder dystonia early myoclonic encephalopathy ectropion embryoma endometriosis of uterus endometriosis esotropia essential hypertension essential tremor female stress incontinence fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia follicular lymphoma glucose intolerance hemopericardium hepatitis B hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus hypertension hypomyelinating leukodystrophy 2 hypomyelinating leukodystrophy 3 hypomyelinating leukodystrophy 4 hypomyelinating leukodystrophy 6 hypomyelinating leukodystrophy 9 ichthyosis interstitial lung disease intracranial aneurysm keratosis follicularis late onset Parkinson's disease leukoencephalopathy with vanishing white matter leukopenia lingual-facial-buccal dyskinesia lipid storage disease liver cirrhosis lymphoma lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression metachromatic leukodystrophy microcephaly mitral valve stenosis mongolian spot monocular esotropia motor peripheral neuropathy movement disease multiple myeloma nervous system disease neuroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus ophthalmoplegia osteoarthritis osteonecrosis osteopetrosis osteosclerosis pancytopenia pathologic nystagmus pericardial effusion placental insufficiency polyhydramnios prediabetes syndrome primary pulmonary hypertension progressive muscular atrophy progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy proteinuria pseudoxanthoma elasticum psoriasis reticulosarcoma schizophrenia seborrheic keratosis secondary Parkinson disease senile degeneration of brain sensorineural hearing loss skin disease speech disorder sphingolipidosis spontaneous ocular nystagmus thrombocytopenia velocardiofacial syndrome
8209	glutamine amidotransferase class 1 domain containing 3	GATD3	Homo sapiens (human)
347862	glutamine amidotransferase class 1 domain containing 1	GATD1	Homo sapiens (human)
57459	GATA zinc finger domain containing 2B	GATAD2B	Homo sapiens (human)

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