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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 **1476 - 1500** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
6820	sulfotransferase family 2B member 1	SULT2B1 Aliases: HSST2	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome achondroplasia acquired hyperkeratosis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 14 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 bacterial sepsis cholestasis ectropion endometrial cancer endometrial carcinoma gallbladder cancer gallbladder carcinoma granuloma annulare hepatocellular carcinoma hypotrichosis ichthyosis keratosis follicularis kidney failure liver cancer mongolian spot obsolete congenital ichthyosiform erythroderma otitis media prostate cancer prostate carcinoma pseudoxanthoma elasticum uterine corpus cancer
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
8867	synaptojanin 1	SYNJ1 Aliases: INPP5G PARK20 inositol polyphosphate-5-phosphatase G phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
8871	synaptojanin 2	SYNJ2 Aliases: INPP5H inositol polyphosphate-5-phosphatase H phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 2	Homo sapiens (human)	Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Parkinson's disease amyotrophic lateral sclerosis 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 breast cancer bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital muscular dystrophy depressive disorder distal myopathy early-onset Parkinson's disease facioscapulohumeral muscular dystrophy giant cell glioblastoma glioblastoma large intestine cancer limb-girdle muscular dystrophy lung cancer lung carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
6888	transaldolase 1	TALDO1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma 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 autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease carbohydrate metabolic disorder childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
6916	thromboxane A synthase 1	TBXAS1 Aliases: CYP5 CYP5A1 THAS TS TXAS TXS cytochrome P450, family 5, subfamily A, polypeptide 1	Homo sapiens (human)	Camurati-Engelmann disease Ghosal hematodiaphyseal syndrome acute myocardial infarction acute necrotizing pancreatitis alcoholic hepatitis alcoholic liver cirrhosis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxia telangiectasia atherosclerosis autosomal recessive osteopetrosis 7 benign mesothelioma brain infarction brain stem infarction breast cancer breast carcinoma cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis essential hypertension glomerulonephritis heart disease hydronephrosis hypertension inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease liver cirrhosis lung benign neoplasm macrocytic anemia malignant mesothelioma malignant pleural mesothelioma membranous glomerulonephritis myelofibrosis myocardial infarction nephritis osteopetrosis osteosclerosis pancytopenia pituitary adenoma pituitary cancer pituitary carcinoma platelet-type bleeding disorder 14 prostate cancer prostate carcinoma pulmonary embolism schizophrenia silent myocardial infarction speech disorder thrombocytopenia thrombosis ulcerative colitis urinary bladder cancer
6996	thymine DNA glycosylase	TDG Aliases: G/T mismatch-specific thymine DNA glycosylase	Homo sapiens (human)	adult medulloblastoma benign ependymoma breast cancer breast carcinoma cancer cellular ependymoma childhood medulloblastoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer hepatitis B high grade glioma large intestine cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma multiple myeloma myxopapillary ependymoma pancreatic cancer pancreatic carcinoma papillary ependymoma rectal benign neoplasm rectum adenocarcinoma rectum cancer skin benign neoplasm skin cancer stomach cancer stomach carcinoma tanycytic ependymoma
9524	trans-2,3-enoyl-CoA reductase	TECR Aliases: MRT14 TER very-long-chain enoyl-CoA reductase	Homo sapiens (human)	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
7007	tectorin alpha	TECTA	Homo sapiens (human)	Stickler syndrome X-linked nonsyndromic deafness autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness breast cancer herpes zoster obsolete autosomal recessive nonsyndromic deafness 105 sensorineural hearing loss trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
6975	tectorin beta	TECTB	Homo sapiens (human)
83639	testis expressed 101	TEX101 Aliases: CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
7021	transcription factor AP-2 beta	TFAP2B	Homo sapiens (human)	Char syndrome angle-closure glaucoma patent ductus arteriosus sleep disorder
7031	trefoil factor 1	TFF1	Homo sapiens (human)	cervical adenocarcinoma colitis ductal carcinoma in situ endometrial cancer endometrial carcinoma endometrial hyperplasia gastric ulcer ovarian cancer ovarian carcinoma prostate cancer signet ring cell adenocarcinoma stomach cancer transitional cell carcinoma urinary bladder cancer
23483	TDP-glucose 4,6-dehydratase	TGDS Aliases: SDR2E1 TDPGD short chain dehydrogenase/reductase family 2E, member 1	Homo sapiens (human)	Alzheimer's disease Catel Manzke syndrome Laron syndrome Marfan syndrome achondroplasia 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 cleft lip cleft palate clubfoot cryptorchidism cystic lymphangioma dementia depressive disorder dextrocardia dysthymic disorder epilepsy hydrocephalus inguinal hernia isolated cleft palate major depressive disorder melancholic depression neurotic disorder obsolete melancholia omphalocele otitis media patent foramen ovale placental insufficiency scoliosis situs inversus temtamy preaxial brachydactyly syndrome tuberous sclerosis umbilical hernia ventricular septal defect visual epilepsy
117145	thioesterase superfamily member 4	THEM4 Aliases: C-terminal modulator protein CTMP	Homo sapiens (human)	amyotrophic lateral sclerosis attention deficit hyperactivity disorder breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma liver cancer lung benign neoplasm lung cancer lung carcinoma mixed glioma pancreatic adenocarcinoma progressive muscular atrophy type 2 diabetes mellitus
284486	thioesterase superfamily member 5	THEM5 Aliases: FLJ37964	Homo sapiens (human)	catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia steatotic liver disease
57103	TP53 induced glycolysis regulatory phosphatase	TIGAR Aliases: TP53-induced glycolysis and apoptosis regulator	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 Fanconi anemia complementation group A Fanconi anemia Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adult T-cell leukemia/lymphoma adult lymphoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood leukemia childhood lymphoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease dementia embryoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma giant cell glioblastoma glioblastoma gliosarcoma hemiplegia hepatocellular carcinoma high grade glioma hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer isolated cleft palate large intestine cancer lateral sclerosis leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma mixed glioma motor neuron disease nasopharynx carcinoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete ymphosarcoma pancreatitis papillary renal cell carcinoma primary cutaneous T-cell non-Hodgkin lymphoma renal carcinoma renal cell carcinoma retinoblastoma sarcomatoid renal cell carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy stomach cancer stomach carcinoma trilateral retinoblastoma ulcerative colitis
25976	TCDD inducible poly(ADP-ribose) polymerase	TIPARP Aliases: ARTD14 DDF1 DKFZP434J214 DKFZp686N0351 PARP-1 PARP-7 PARP7 RM1 pART14	Homo sapiens (human)	acoustic neuroma alcohol dependence alcohol use disorder angiomatous meningioma benign meningioma cancer cerebral convexity meningioma cervical cancer cervix carcinoma clear cell meningioma embryoma fibrous meningioma hepatitis A hepatitis intraorbital meningioma intraventricular meningioma meningioma meningothelial meningioma microcystic meningioma olfactory groove meningioma ovarian cancer parasagittal meningioma pituitary adenoma psammomatous meningioma secretory meningioma spinal meningioma transitional meningioma
26007	triokinase and FMN cyclase	TKFC Aliases: DKFZP586B1621 FAD-AMP lyase (cyclizing) NET45	Homo sapiens (human)	cataract diabetes mellitus diabetic ketoacidosis liver disease type 2 diabetes mellitus
7086	transketolase	TKT Aliases: Wernicke-Korsakoff syndrome	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 Crohn's colitis Crohn's disease Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wernicke encephalopathy Wernicke-Korsakoff syndrome adenocarcinoma adenoma adrenal cortex cancer alcohol dependence alcohol use disorder amnestic 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 beriberi breast cancer breast carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma chronic kidney disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cribriform carcinoma critical illness polyneuropathy cystinuria diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy dry beriberi embryoma galactosemia gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder insulinoma intellectual disability large intestine cancer learning disability liver cancer liver disease meningoencephalitis mixed glioma multiple sclerosis myeloproliferative disorder with eosinophilia nasopharynx carcinoma neurodegenerative disease neuropathy obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma patent ductus arteriosus patent foramen ovale pellagra peripheral nervous system disease polyneuropathy rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma thiamine deficiency disease thiamine-responsive megaloblastic anemia syndrome thyroid gland anaplastic carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis 1 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 ventricular septal defect
8277	transketolase like 1	TKTL1 Aliases: TKR TKT2	Homo sapiens (human)	Aicardi-Goutieres syndrome Crouzon syndrome adenocarcinoma adenoma arthritis arthropathy breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral palsy cervical adenocarcinoma cervical cancer cervix carcinoma chronic myeloid leukemia cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma embryoma embryonal cancer endometrial stromal sarcoma esophagus squamous cell carcinoma gastrointestinal stromal tumor germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma granulosa cell tumor head and neck squamous cell carcinoma hemiplegia hepatitis B hepatocellular carcinoma high grade glioma isolated cleft palate large intestine cancer leiomyoma liver cancer lymphoma melanoma mixed glioma morbid obesity mucinous adenocarcinoma myofibroma nasopharynx carcinoma obesity obsolete ymphosarcoma osteoarthritis papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma seminoma skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy squamous cell carcinoma stomach cancer stomach carcinoma testicular cancer testicular germ cell cancer thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine fibroid
84076	transketolase like 2	TKTL2 Aliases: DKFZP434L1717 FLJ32975 similar to transketolase	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma large intestine cancer liver cancer type 2 diabetes mellitus
7096	toll like receptor 1	TLR1	Homo sapiens (human)	IgA glomerulonephritis aspergillosis asthma leprosy perinatal necrotizing enterocolitis pulmonary tuberculosis pyelonephritis tuberculosis
81793	toll like receptor 10	TLR10	Homo sapiens (human)	asthma
7097	toll like receptor 2	TLR2	Homo sapiens (human)	Behcet's disease Kuhnt-Junius degeneration acne acute necrotizing pancreatitis allergic rhinitis alveolar echinococcosis anogenital venereal wart anterior uveitis asthma atopic dermatitis atrial fibrillation bacterial pneumonia breast cancer carotid stenosis cholesteatoma of middle ear cholesteatoma colorectal cancer cutaneous leishmaniasis cystic echinococcosis dermatomyositis diffuse scleroderma dry eye syndrome end stage renal disease eye disease gastroesophageal reflux disease hepatocellular carcinoma ileitis keratitis keratoconjunctivitis kidney failure leprosy lung disease mastoiditis meningococcal meningitis molluscum contagiosum otitis media pancreatitis perinatal necrotizing enterocolitis prostate cancer psoriasis pulmonary sarcoidosis pulmonary tuberculosis renal fibrosis rhinitis seborrheic dermatitis severe acute respiratory syndrome sinusitis skin papilloma suppurative otitis media tuberculosis type 1 diabetes mellitus urinary bladder cancer urinary tract infection vitiligo

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