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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 **1001 - 1025** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
4706	NADH:ubiquinone oxidoreductase subunit AB1	NDUFAB1 Aliases: ACP ACP1 FASN2A SDAP acyl carrier protein, mitochondrial complex I SDAP subunit	Homo sapiens (human)	Alzheimer's disease HCL-V Lynch syndrome Marfan syndrome Richter's syndrome Wilson disease X-linked dilated cardiomyopathy actinic keratosis adamantinous craniopharyngioma adult lymphoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxic cerebral palsy atherosclerosis brain cancer cancer central nervous system lymphoma central retinal vein occlusion cerebral infarction cerebrovascular disease childhood lymphoma chronic lymphocytic leukemia congenital hemolytic anemia congestive heart failure coronary artery disease craniopharyngioma cystinuria dementia dental caries dentin sensitivity dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endometrial cancer endometrial carcinoma favism galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease gonorrhea hairy cell leukemia hemochromatosis hereditary elliptocytosis iron metabolism disease lymphoma neurodegeneration with brain iron accumulation neurodegenerative disease nutmeg liver obesity obsolete ymphosarcoma osteoporosis papillary craniopharyngioma root caries situs inversus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tuberous sclerosis uterine corpus cancer
79661	nei like DNA glycosylase 1	NEIL1 Aliases: DNA endonuclease eight-like glycosylase 1 FLJ22402 FPG1 NEI1 hFPG1	Homo sapiens (human)	Alzheimer's disease Behcet's disease Chandler syndrome Fanconi anemia complementation group A Fanconi anemia Fuchs' endothelial dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acquired immunodeficiency syndrome bile duct adenocarcinoma bile duct carcinoma cancer carcinoma cerebral infarction cerebrovascular disease cholangiocarcinoma chromosome 15q24 deletion syndrome colorectal cancer common variable immunodeficiency corneal disease depressive disorder diabetes mellitus distal arthrogryposis dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hyperlipidemia gallbladder disease glucose intolerance head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease hyperinsulinism intrahepatic cholangiocarcinoma keratoconus large intestine cancer liver cancer liver disease lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression multiple myeloma neurotic disorder obesity obsolete melancholia prediabetes syndrome primary sclerosing cholangitis progeria sarcomatoid carcinoma sclerosing cholangitis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus
252969	nei like DNA glycosylase 2	NEIL2 Aliases: FLJ31644 MGC2832 MGC4505 NEH2	Homo sapiens (human)	breast cancer bronchus cancer bronchus carcinoma cancer colorectal cancer embryoma hepatitis C hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma oropharynx cancer polycystic ovary syndrome squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma
55247	nei like DNA glycosylase 3	NEIL3 Aliases: FLJ10858 FPG2 ZGRF3 hFPG2 hNEI3 zinc finger, GRF-type containing 3	Homo sapiens (human)	Fanconi anemia acute myocardial infarction basal cell carcinoma cancer coronary thrombosis differentiated thyroid gland carcinoma embryoma giant cell glioblastoma glioblastoma glomerulonephritis hepatocellular carcinoma kidney disease liver cancer myocardial infarction nephritis silent myocardial infarction
4758	neuraminidase 1	NEU1 Aliases: sialidase-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 Crohn's colitis Crohn's disease Ewing sarcoma of bone GM1 gangliosidosis type 1 GM1 gangliosidosis IgA glomerulonephritis Laron syndrome Marfan syndrome Paget's disease of bone Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia acquired hyperkeratosis adenocarcinoma adenoma allergic rhinitis anaplastic astrocytoma arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease aspartylglucosaminuria atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma biliary tract cancer bladder urothelial carcinoma blepharospasm bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cataract cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma cholangiocarcinoma chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease cribriform carcinoma cutaneous Paget's disease dentatorubral-pallidoluysian atrophy dermoid cyst of ovary dissociated nystagmus early myoclonic encephalopathy embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma endomyocardial fibrosis enterocele epilepsy fibrillary astrocytoma focal hand dystonia fucosidosis galactosialidosis gastroesophageal junction adenocarcinoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance glycoproteinosis granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza inguinal hernia intellectual disability intrahepatic cholangiocarcinoma invasive ductal carcinoma juvenile pilocytic astrocytoma kidney disease large intestine cancer learning disability livedoid vasculitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease malignant astrocytoma mammary Paget's disease melanoma meningitis microphthalmia mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia nephritis nervous system cancer nonpapillary renal cell carcinoma osteochondrodysplasia osteosarcoma ovarian cancer ovarian carcinoma ovary adenocarcinoma papillary carcinoma papillary renal cell carcinoma pathologic nystagmus pilocytic astrocytoma postinflammatory pulmonary fibrosis prediabetes syndrome progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy prostate cancer prostate carcinoma proteinuria protoplasmic astrocytoma pulmonary fibrosis recurrent corneal erosion renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scoliosis sebaceous carcinoma sensorineural hearing loss serous cystadenocarcinoma situs inversus skin melanoma speech disorder spontaneous ocular nystagmus steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tarsal-carpal coalition syndrome transitional cell carcinoma tuberous sclerosis tubular adenocarcinoma ulcerative colitis uterine corpus cancer vascular skin disease vasomotor rhinitis visual epilepsy vitiligo
4759	neuraminidase 2	NEU2 Aliases: N-acetyl-alpha-neuraminidase 2 SIAL2	Homo sapiens (human)	allergic rhinitis cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma rhabdomyosarcoma stomach cancer stomach carcinoma vasomotor rhinitis
10825	neuraminidase 3	NEU3	Homo sapiens (human)	Tay-Sachs disease alternating hemiplegia of childhood amnestic disorder autonomic neuropathy cancer carcinoma central nervous system disease chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dissociative amnesia embryoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia large intestine cancer lung cancer lung non-small cell carcinoma nervous system disease ovarian cancer ovarian carcinoma ovarian clear cell adenocarcinoma ovary adenocarcinoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma
129807	neuraminidase 4	NEU4	Homo sapiens (human)	cancer embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
55768	N-glycanase 1	NGLY1 Aliases: FLJ11005 PNG-1 PNG1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase peptide:N-glycanase	Homo sapiens (human)	Cogan syndrome NGLY1-deficiency Unverricht-Lundborg syndrome West syndrome alternating exotropia amyotrophic lateral sclerosis anhidrosis antithrombin III deficiency atrophic gastritis blepharospasm cancer cerebral degeneration choreatic disease cone-rod dystrophy congenital afibrinogenemia congenital ptosis corneal neovascularization corneal ulcer craniosynostosis critical illness polyneuropathy diffuse interstitial keratitis early myoclonic encephalopathy embryoma epilepsy exotropia factor V deficiency factor VII deficiency focal epilepsy focal hand dystonia fundus albipunctatus hydrocephalus hypertropia hypohidrosis inflammatory and toxic neuropathy lingual-facial-buccal dyskinesia mechanical strabismus melanoma meningoencephalitis microcephaly monocular exotropia movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive sleep apnea ophthalmoplegia optic atrophy osteoporosis peripheral nervous system disease placental insufficiency polyneuropathy progressive muscular atrophy protein C deficiency protein S deficiency ptosis recurrent corneal erosion retinitis pigmentosa scoliosis skin melanoma stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability type 10 thrombophilia visual epilepsy
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Homo sapiens (human)	Lafora disease
4864	NPC intracellular cholesterol transporter 1	NPC1 Aliases: SLC65A1	Homo sapiens (human)	Niemann-Pick disease type C1 Niemann-Pick disease
80896	N-acetylneuraminate pyruvate lyase	NPL Aliases: DHDPS1 NPL1 dihydrodipicolinate synthetase homolog 1 (E. coli)	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 Ewing sarcoma Pick's disease Reye syndrome alcohol dependence alcohol use disorder atopic dermatitis bipolar disorder cerebral degeneration cholestasis congestive heart failure dermatitis epilepsy essential hypertension generalized epilepsy with febrile seizures plus hypertension idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease influenza juvenile myoclonic epilepsy myopathy obsolete major affective disorder 1 obsolete major affective disorder 2 panic disorder prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss ulcerative colitis visual epilepsy
4886	neuropeptide Y receptor Y1	NPY1R	Homo sapiens (human)	amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
9572	nuclear receptor subfamily 1 group D member 1	NR1D1	Homo sapiens (human)	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
123904	neuritin 1 like	NRN1L Aliases: MRCC2446 UNQ2446	Homo sapiens (human)	epilepsy visual epilepsy
50814	NAD(P) dependent steroid dehydrogenase-like	NSDHL Aliases: H105e3 SDR31E1 XAP104 short chain dehydrogenase/reductase family 31E, member 1	Homo sapiens (human)	Bloch-Sulzberger syndrome CHILD syndrome CK syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia cancer chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
4907	5'-nucleotidase ecto	NT5E Aliases: CALJA CD73 eN eNT	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 Baraitser-Winter syndrome Chagas disease Crohn's colitis Crohn's disease Down syndrome Fabry disease Fraser syndrome 1 Fraser syndrome Gilbert syndrome Goldenhar syndrome Goodpasture syndrome Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Jervell-Lange Nielsen syndrome Kallmann syndrome MHC class II deficiency Meniere's disease Moebius syndrome Muckle-Wells syndrome Muenke Syndrome Nance-Horan syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Takayasu's arteritis Troyer syndrome Turner syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome X-linked agammaglobulinemia acinar cell carcinoma acoustic neuroma acute lymphoblastic leukemia acute maxillary sinusitis acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosine deaminase deficiency adult acute lymphocytic leukemia adult epithelioid sarcoma adult lymphoma adult medulloblastoma adult respiratory distress syndrome agammaglobulinemia allergic asthma allergic rhinitis amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 angiomatous meningioma angle-closure glaucoma ankylosing spondylitis anterior horn cell disease anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arterial tortuosity syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thyroiditis autosomal recessive distal hereditary motor neuronopathy 1 basal cell carcinoma benign meningioma benign mesothelioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma brain cancer branchiootic syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma calciphylaxis cancer carcinoma cardiac arrest cardiovascular system disease cecum adenocarcinoma celiac disease central nervous system cancer central nervous system origin vertigo cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood epithelioid sarcoma childhood leukemia childhood lymphoma childhood medulloblastoma cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic lymphocytic leukemia chronic maxillary sinusitis chronic obstructive pulmonary disease chronic rhinitis chylomicron retention disease clear cell meningioma clear cell renal cell carcinoma cleft palate colitis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital hemolytic anemia congenital hypogammaglobulinemia congenital nystagmus congestive heart failure connective tissue disease corneal disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma depressive disorder diffuse large B-cell lymphoma dissociated nystagmus double outlet right ventricle dysthymic disorder embryoma encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis enthesopathy epilepsy esophagitis esophagus squamous cell carcinoma eunuchism fibromyalgia fibrous meningioma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gastritis gastroenteritis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma gonadal dysgenesis granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hepatitis hepatocellular carcinoma hereditary arterial and articular multiple calcification syndrome high grade glioma hydrocephalus hyperthyroidism 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 idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated cleft palate 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 keratoconus keratosis follicularis kidney cancer large intestine cancer laryngeal disease laryngeal squamous cell carcinoma lateral sclerosis lipid storage disease liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma major depressive disorder malignant mesothelioma mastoiditis maxillary sinusitis medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma mongolian spot motor neuron disease mucocele of salivary gland mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis myocardial infarction neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder newborn respiratory distress syndrome non-suppurative otitis media nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea olfactory groove meningioma orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pathologic nystagmus peptic esophagitis pericarditis periodontitis peripheral nervous system disease peripheral vascular disease pituitary adenoma polyarteritis nodosa polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum psoriasis pulmonary fibrosis pustulosis of palm and sole pycnodysostosis rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma secretory meningioma senile degeneration of brain sensorineural hearing loss septooptic dysplasia severe combined immunodeficiency sickle cell anemia silent myocardial infarction skin melanoma spinal meningioma spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma suppurative periapical periodontitis thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tonsillitis tracheal disease transitional meningioma trypanosomiasis tuberculosis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer vasculitis vasomotor rhinitis visual epilepsy
56953	5',3'-nucleotidase, mitochondrial	NT5M Aliases: dNT-2 dNT2 mdN	Homo sapiens (human)	Miller-Dieker lissencephaly syndrome Smith-Magenis syndrome
4913	nth like DNA glycosylase 1	NTHL1 Aliases: NTH1 OCTS3	Homo sapiens (human)	B-cell lymphoma Fanconi anemia complementation group D2 Fanconi anemia Langerhans-cell histiocytosis acoustic neuroma actinic keratosis adenocarcinoma adenoma angiomatous meningioma autosomal recessive intellectual developmental disorder basal cell carcinoma benign meningioma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma clear cell meningioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatosis papulosa nigra duodenum adenocarcinoma embryoma endometrial cancer endometrial carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 3 familial adenomatous polyposis fibrous meningioma follicular adenoma intraorbital meningioma intraventricular meningioma inverted follicular keratosis islet cell tumor large intestine cancer laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma melanoacanthoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma non-Hodgkin lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cyst pancreatic adenocarcinoma papillary adenoma parasagittal meningioma pituitary adenoma psammomatous meningioma rectal benign neoplasm rectum cancer reticulosarcoma sarcomatoid carcinoma seborrheic dermatitis seborrheic keratosis secretory meningioma skin benign neoplasm skin cancer skin disease spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma transitional meningioma tuberous sclerosis 2 tuberous sclerosis urinary bladder cancer uterine corpus cancer
50863	neurotrimin	NTM Aliases: CEPU-1 HNT IGLON2 IgLON family member 2 NTRI neurotrimin	Homo sapiens (human)	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
11164	nudix hydrolase 5	NUDT5 Aliases: YSA1H hYSAH1	Homo sapiens (human)	breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
60506	nyctalopin	NYX Aliases: CLRP CSNB1A	Homo sapiens (human)	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
221443	O-acyl-ADP-ribose deacylase 1	OARD1 Aliases: MGC19570 TARG1 dJ34B21.3 terminal ADP-ribose protein glycohydrolase 1	Homo sapiens (human)	acute myeloid leukemia neurodegenerative disease stomach cancer stomach carcinoma
4938	2'-5'-oligoadenylate synthetase 1	OAS1	Homo sapiens (human)	primary immunodeficiency disease

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