GlyCosmos Portal

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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 **801 - 825** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
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
8790	fucose-1-phosphate guanylyltransferase	FPGT Aliases: GFPP	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
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
148738	hemojuvelin BMP co-receptor	HJV Aliases: HFE2A JH RGMC haemojuvelin hemojuvelin repulsive guidance molecule c	Homo sapiens (human)	Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kallmann syndrome Meckel syndrome 8 Sheehan syndrome Wilson disease X-linked dilated cardiomyopathy amenorrhea anaplastic astrocytoma androgen insensitivity syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autosomal recessive polycystic kidney disease azoospermia bacterial infectious disease beta thalassemia breast cancer breast carcinoma cardiomyopathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma cholestasis chronic kidney disease congenital hypothyroidism congenital nongoitrous hypothyroidism 4 congestive heart failure coronary artery disease diabetes mellitus diabetic ketoacidosis 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 endomyocardial fibrosis essential hypertension essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma hemochromatosis type 1 hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatitis C hepatocellular carcinoma high grade glioma hypertension hypertrophic cardiomyopathy hypogonadism 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 impotence infertility iron metabolism disease 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 juvenile pilocytic astrocytoma kwashiorkor liver cancer lung squamous cell carcinoma malignant astrocytoma marasmus microcytic anemia middle cerebral artery infarction muscular dystrophy myelodysplastic syndrome myxedema neurogenic arthropathy nutrition disease obesity osteoporosis panhypopituitarism pilocytic astrocytoma polycystic kidney disease 4 porphyria cutanea tarda premature ejaculation protein-energy malnutrition protoplasmic astrocytoma psychologic dyspareunia sick sinus syndrome steatotic liver disease subependymal giant cell astrocytoma thalassemia
2717	galactosidase alpha	GLA Aliases: GALA	Homo sapiens (human)	Fabry disease Gaucher's disease Goodpasture syndrome Horner's syndrome Laron syndrome Meckel syndrome Moyamoya disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Riley-Day syndrome Takayasu's arteritis X-linked agammaglobulinemia Zollinger-Ellison syndrome achondroplasia acquired hyperkeratosis acute myocardial infarction allergic asthma anemia angiokeratoma anhidrosis antithrombin III deficiency anxiety disorder arthritis arthropathy asthma atrial fibrillation atrioventricular block autosomal dominant polycystic kidney disease bacterial vaginosis breast cancer breast fibrocystic disease brucellosis cancer cardiomyopathy cardiovascular system disease cataract central nervous system origin vertigo cerebral infarction cerebrovascular disease chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease congenital hypogammaglobulinemia congestive heart failure corneal dystrophy coronary thrombosis cystinuria depressive disorder diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism dysthymic disorder elephantiasis endomyocardial fibrosis epilepsy erythromelalgia essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial mediterranean fever familial nephrotic syndrome fibromyalgia galactosemia generalized anxiety disorder glaucoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granulomatosis with polyangiitis heart disease hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypohidrosis influenza inherited metabolic disorder interstitial nephritis intrinsic asthma keratosis follicularis kidney disease kidney failure late onset Parkinson's disease lipid storage disease lipoid nephrosis lung disease lymphedema lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression mevalonic aciduria microglandular adenosis mitral valve insufficiency mitral valve prolapse mongolian spot multiple sclerosis myocardial infarction myositis nephritis nephrosis nephrotic syndrome neurohypophyseal diabetes insipidus neuropathy neurotic disorder obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease optic atrophy osteoarthritis papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease pneumonia polyarteritis nodosa polyneuropathy priapism protein C deficiency protein S deficiency proteinuria pseudoxanthoma elasticum pyelitis pyelonephritis pyoureter recurrent corneal erosion renal infectious disease sensorineural hearing loss sick sinus syndrome silent myocardial infarction sphingolipidosis thrombophilia thyroid gland papillary carcinoma transient cerebral ischemia tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia vaginitis vascular disease vertebrobasilar insufficiency visual epilepsy vitamin K deficiency bleeding vulvitis vulvovaginal candidiasis vulvovaginitis
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
8526	diacylglycerol kinase epsilon	DGKE Aliases: DAGK6 DGK	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute kidney failure allergic asthma asthma atypical hemolytic-uremic syndrome breast cancer cancer capillary disease cardiovascular system disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy embryoma epilepsy familial nephrotic syndrome fundus albipunctatus glomerulonephritis heart disease hemolytic anemia hemolytic-uremic syndrome hereditary hemorrhagic telangiectasia intrinsic asthma kidney disease kidney failure large intestine cancer lipoid nephrosis liver cirrhosis membranoproliferative glomerulonephritis mitochondrial DNA depletion syndrome nephritis nephrosis nephrotic syndrome type 7 nephrotic syndrome obesity proteinuria pyoureter retinitis pigmentosa telangiectasis thrombocytopenia thrombotic thrombocytopenic purpura uremia visual epilepsy
26253	C-type lectin domain family 4 member E	CLEC4E Aliases: MINCLE Macrophage-inducible C-type lectin	Homo sapiens (human)	acute myocardial infarction allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis coronary thrombosis depressive disorder dysthymic disorder intrinsic asthma keratitis keratoconjunctivitis major depressive disorder melancholic depression multiple sclerosis mycotic corneal ulcer myocardial infarction neurotic disorder obsolete melancholia pulmonary tuberculosis rheumatoid arthritis silent myocardial infarction tuberculosis tuberculous pneumothorax
2762	GDP-mannose 4,6-dehydratase	GMDS Aliases: GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	Homo sapiens (human)	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IIc embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
5331	phospholipase C beta 3	PLCB3	Homo sapiens (human)	acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma cancer coronary thrombosis cribriform carcinoma cystic fibrosis dermatitis diabetes mellitus diabetic ketoacidosis essential hypertension extragonadal germ cell cancer granular cell carcinoma hyperparathyroidism hypertension lung cancer lung disease lung non-small cell carcinoma multiple endocrine neoplasia type 1 myocardial infarction neuroendocrine carcinoma neuroendocrine tumor obesity osteitis fibrosa silent myocardial infarction spondylometaphyseal dysplasia with corneal dystrophy tubular adenocarcinoma type 2 diabetes mellitus vitiligo
4595	mutY DNA glycosylase	MUTYH Aliases: MYH	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Hantavirus hemorrhagic fever with renal syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lynch syndrome Muir-Torre syndrome Peutz-Jeghers syndrome acoustic neuroma adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma age related macular degeneration anal carcinoma in situ angiomatous meningioma arthritis arthropathy benign meningioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral convexity meningioma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma chromosome 10q23 deletion syndrome clear cell meningioma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 2 familial adenomatous polyposis female breast carcinoma fibrous meningioma follicular adenoma gastroenteritis gastrointestinal system cancer gastrointestinal system disease gliosarcoma granular cell carcinoma hair follicle neoplasm head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile polyposis syndrome large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma myeloproliferative neoplasm nervous system cancer neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurotic disorder obsolete melancholia olfactory groove meningioma osteoarthritis ovarian cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma parasagittal meningioma pilomatrixoma pituitary adenoma primary open angle glaucoma proctitis prostate cancer prostate carcinoma psammomatous meningioma rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis sarcomatoid carcinoma sebaceous adenocarcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma in situ stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma transitional meningioma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer von Hippel-Lindau disease
50614	polypeptide N-acetylgalactosaminyltransferase 9	GALNT9 Aliases: GALNAC-T9 polypeptide GalNAc transferase 9	Homo sapiens (human)	breast cancer breast carcinoma cancer neuroblastoma
388512	C-type lectin domain containing 17A	CLEC17A Aliases: FLJ45910 prolectin	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia
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
10715	ceramide synthase 1	CERS1 Aliases: LAG1 UOG1	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis blepharospasm cancer central nervous system cancer congestive heart failure coronary artery disease dementia dengue disease dentatorubral-pallidoluysian atrophy double outlet right ventricle early myoclonic encephalopathy embryoma focal hand dystonia gliosarcoma hand, foot and mouth disease head and neck squamous cell carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability learning disability malaria mixed glioma multiple types of congenital heart defects 6 neuroblastoma papillary adenocarcinoma papillary renal cell carcinoma primary spontaneous pneumothorax progressive myoclonus epilepsy 4 progressive myoclonus epilepsy 8 progressive myoclonus epilepsy steatotic liver disease tetralogy of Fallot thyroid gland papillary carcinoma ulcerative colitis viral infectious disease visceral heterotaxy visual epilepsy yellow fever
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia 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 brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
64921	CAS1 domain containing 1	CASD1	Homo sapiens (human)
9663	lipin 2	LPIN2 Aliases: KIAA0249	Homo sapiens (human)	Chanarin-Dorfman syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia SAPHO syndrome acne agranulocytosis allergic asthma anemia asthma autosomal recessive congenital ichthyosis 1 autosomal recessive osteopetrosis 7 cancer chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia congestive heart failure dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism familial mediterranean fever familial periodic paralysis fibromyalgia gastrointestinal system disease glomerulonephritis granular corneal dystrophy 2 ichthyosis inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrinsic asthma keratosis follicularis leukopenia lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy macrocytic anemia mevalonic aciduria microcytic anemia mongolian spot myoglobinuria myopathy myopia myositis nephritis neutropenia obesity obsolete congenital ichthyosiform erythroderma osteomyelitis osteopetrosis osteosclerosis prostate cancer prostate carcinoma proteinuria pseudoxanthoma elasticum relapsing fever rheumatoid arthritis severe congenital neutropenia synovitis tenosynovitis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue type 2 diabetes mellitus ulcerative colitis
23556	phosphatidylinositol glycan anchor biosynthesis class N	PIGN Aliases: GPI ethanolamine phosphate transferase 1 MCD4 PIG-N	Homo sapiens (human)	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia 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 autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
6783	sulfotransferase family 1E member 1	SULT1E1 Aliases: EST	Homo sapiens (human)	Alzheimer's disease Axenfeld-Rieger syndrome type 2 Creutzfeldt-Jakob disease DiGeorge syndrome Down syndrome Laron syndrome Marfan syndrome Richter's syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction acute myocarditis adult lymphoma adult medulloblastoma adult oligodendroglioma alcoholic hepatitis amyotrophic lateral sclerosis androgen insensitivity syndrome ankylosing spondylitis aortic disease arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autosomal recessive limb-girdle muscular dystrophy type 2C bacterial sepsis bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cardiovascular system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic fatigue syndrome chronic lymphocytic leukemia colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis coronary thrombosis craniosynostosis cystic fibrosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysentery dysthymic disorder embryoma encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis essential hypertension eye disease familial hypertrophic cardiomyopathy gallbladder disease gastric adenocarcinoma glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy inferior myocardial infarction inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermediate coronary syndrome kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mitochondrial metabolism disease mitral valve stenosis mixed oligodendroglioma-astrocytoma multiple endocrine neoplasia type 1 myocardial infarction nephritis nephrosis neurotic disorder nodular prostate obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma peripheral artery disease polycystic ovary syndrome pompholyx primary hyperoxaluria primary open angle glaucoma primary pulmonary hypertension progressive muscular atrophy proliferative type fibrocystic change of breast prostate cancer prostate carcinoma prostatic adenoma pyoureter retinal disease retinitis schizophrenia 1 schizophrenia scleroderma severe acute respiratory syndrome silent myocardial infarction situs inversus steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tetralogy of Fallot thymic carcinoma thymoma transient cerebral ischemia 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 ulcerative colitis uterine corpus cancer velocardiofacial syndrome vertebrobasilar insufficiency
200185	keratinocyte associated protein 2	KRTCAP2 Aliases: KCP2	Homo sapiens (human)
1312	catechol-O-methyltransferase	COMT	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 Balo concentric sclerosis Clostridium difficile colitis Cockayne syndrome DiGeorge syndrome Dowling-Degos disease Down syndrome Gilles de la Tourette syndrome Graves' disease Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kleine-Levin syndrome Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Lynch syndrome Meckel syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wolfram syndrome 1 Wolfram syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired immunodeficiency syndrome acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer adrenoleukodystrophy adult lymphoma agnosia alcohol dependence alcohol use disorder alexia allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anencephaly anorexia nervosa antisocial personality disorder anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis 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 autism spectrum disorder autistic disorder autonomic neuropathy autosomal dominant polycystic kidney disease avoidant personality disorder bipolar disorder bladder carcinoma borderline personality disorder breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma bulimia nervosa bullous congenital ichthyosiform erythroderma cancer cannabis abuse cannabis dependence cardiovascular system disease carpal tunnel syndrome cataract central nervous system disease central nervous system lymphoma central nervous system origin vertigo central sleep apnea cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood disintegrative disease childhood kidney cell carcinoma childhood lymphoma choanal atresia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate clubfoot cocaine abuse cocaine dependence cognitive disorder collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus conduct disorder congenital diarrhea 5 with tufting enteropathy congenital hypothyroidism congenital ptosis conversion disorder corneal neovascularization coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma critical illness polyneuropathy cryptorchidism degenerative disc disease delusional disorder dementia dental caries dental fluorosis dentin caries depressive disorder desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health dissociative disorder distal myopathy double outlet right ventricle drug dependence drug psychosis duodenum cancer dyslexia dysthymic disorder dystonia eating disorder eclampsia embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epilepsy episodic kinesigenic dyskinesia 1 episodic kinesigenic dyskinesia 2 esophagitis esophagus squamous cell carcinoma essential hypertension eumycotic mycetoma female breast carcinoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroesophageal reflux disease generalized anxiety disorder glaucoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hepatitis C hepatocellular carcinoma heroin dependence herpes simplex holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hydrocephalus hypercalcemia hypertension hypertensive encephalopathy hyperthyroidism hypertropia hypoparathyroidism hypospadias hypothyroidism imperforate anus impulse control disorder inappropriate ADH syndrome inflammatory and toxic neuropathy inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma irritable bowel syndrome isolated cleft palate kidney cancer kleptomania large intestine cancer late onset Parkinson's disease lateral meningocele syndrome learning disability leiomyoma lingual-facial-buccal dyskinesia lissencephaly liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder male infertility mechanical strabismus melancholic depression meningoencephalitis microcephaly microglandular adenosis microphthalmia migraine without aura migraine mitral valve stenosis mood disorder morphine dependence multiple sclerosis myelitis myelomeningocele myeloproliferative disorder with eosinophilia myocardial infarction myofibroma myositis ossificans myositis myxedema narcissistic personality disorder narcolepsy neonatal abstinence syndrome nephrocalcinosis nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nicotine dependence nodular prostate non-Hodgkin lymphoma nutmeg liver obesity obsessive-compulsive disorder obsessive-compulsive personality disorder obsolete T-cell lymphoblastic leukemia/lymphoma obsolete constipation obsolete dyspepsia obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea omphalocele ophthalmoplegia opiate dependence optic atrophy osteoarthritis osteochondritis dissecans osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary renal cell carcinoma paranoid schizophrenia parapsoriasis patent ductus arteriosus patent foramen ovale pathological gambling peptic esophagitis peripheral nervous system disease pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency polycystic ovary syndrome polyhydramnios polyneuropathy post-traumatic stress disorder pre-eclampsia prediabetes syndrome premature ejaculation premature menopause primary immunodeficiency disease primary ovarian insufficiency progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism psoriasis psychotic disorder ptosis purpura pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent hypersomnia renal carcinoma renal cell carcinoma renal hypoplasia reticulate acropigmentation of Kitamura reticulosarcoma retrograde amnesia rumination disorder sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder schizotypal personality disorder scoliosis seasonal affective disorder seborrheic dermatitis seborrheic infantile dermatitis seborrheic keratosis secondary Parkinson disease senile degeneration of brain sickle cell anemia silent myocardial infarction small intestine cancer social phobia somatization disorder somatoform disorder spina bifida sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma strabismus subacute delirium substance abuse substance-related disorder systemic lupus erythematosus tethered spinal cord syndrome tetralogy of Fallot thrombocytopenia thrombophilia thyrotoxicosis tibial muscular dystrophy tongue squamous cell carcinoma transient myeloproliferative syndrome tricuspid atresia tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicose veins velocardiofacial syndrome ventricular septal defect vesicoureteral reflux visual epilepsy vitiligo withdrawal disorder 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
7364	UDP glucuronosyltransferase family 2 member B7	UGT2B7 Aliases: UGT2B9	Homo sapiens (human)	agnosia bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardia cancer cardiovascular system disease clear cell renal cell carcinoma colorectal cancer colorectal carcinoma congestive heart failure diarrhea embryoma endometrial cancer endometrial carcinoma epilepsy gallbladder disease heart disease hepatitis hepatocellular carcinoma kidney cancer large intestine cancer leukopenia liver cancer liver carcinoma liver disease renal carcinoma renal cell carcinoma sarcomatoid carcinoma sickle cell anemia transitional cell carcinoma tuberculosis urinary bladder cancer uterine corpus cancer visual epilepsy
972	CD74 molecule	CD74 Aliases: CLIP HLA-DR-gamma Ia-associated invariant chain MHC HLA-DR gamma chain class II MHC-associated invariant chain peptide gamma chain of class II antigens	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 Pick's disease Reye syndrome Richter's syndrome acrodermatitis acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma alcoholic hepatitis amnestic disorder amyloidosis anaplastic astrocytoma ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome bacterial sepsis basal cell carcinoma benign mesothelioma bladder carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease carotid artery thrombosis carotid stenosis central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease chikungunya childhood cerebral astrocytoma childhood lymphoma chromophobe renal cell carcinoma chromosome 5q deletion syndrome chronic fatigue syndrome chronic lymphocytic leukemia chronic obstructive pulmonary disease classic pulmonary blastoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy coronary artery disease degenerative disc disease dengue hemorrhagic fever dermatitis diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma disease of metabolism embryoma encephalitis encephalomyelitis endometriosis of uterus endometriosis fibrillary astrocytoma follicular adenoma fundus albipunctatus gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis heart disease hematologic cancer hepatitis hepatocellular carcinoma high grade glioma immune system disease inflammatory bowel disease 1 inflammatory bowel disease juvenile pilocytic astrocytoma kidney cancer kidney disease lepromatous leprosy liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus nephritis lymphoma malignant astrocytoma malignant fibrous histiocytoma malignant mesothelioma malignant pleural mesothelioma mantle cell lymphoma melanoma microcystic adenoma mixed glioma mucinous adenocarcinoma multiple myeloma multiple sclerosis myelitis myositis nephritis nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma periodontitis pilocytic astrocytoma placental insufficiency pneumonia primary biliary cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma pulmonary emphysema red color blindness renal carcinoma renal cell carcinoma retinal disease retinitis pigmentosa retinitis retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma sebaceous carcinoma skin melanoma spondyloarthropathy spondylosis squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma 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 C thymoma ulcerative colitis urinary bladder cancer vertebrobasilar insufficiency viral infectious disease
84317	coiled-coil domain containing 115	CCDC115 Aliases: FLJ30131 MGC12981 ccp1	Homo sapiens (human)	Wilson disease cancer congenital disorder of glycosylation type IIo congenital disorder of glycosylation gallbladder disease hemochromatosis iron metabolism disease liver disease male infertility measles neuroblastoma neurodegenerative disease prostate adenocarcinoma prostate cancer prostate carcinoma

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