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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 **526 - 550** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
2203	fructose-bisphosphatase 1	FBP1	Homo sapiens (human)	B-cell lymphoma Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Rett syndrome acute myocardial infarction bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cryptococcosis cystinuria diabetes mellitus diabetic ketoacidosis diarrhea diffuse large B-cell lymphoma distal arthrogryposis embryoma epilepsy follicular lymphoma fructose-1,6-bisphosphatase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatitis C hepatitis hepatocellular carcinoma high grade glioma hydrocephalus hyperuricemia hypoglycemia intellectual disability intrahepatic cholangiocarcinoma lactic acidosis large intestine cancer learning disability liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maturity-onset diabetes of the young microphthalmia mixed glioma myocardial infarction neonatal jaundice nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia silent myocardial infarction situs inversus squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis type 2 diabetes mellitus viral infectious disease visual epilepsy
284348	LY6/PLAUR domain containing 5	LYPD5 Aliases: FLJ30469	Homo sapiens (human)	B-cell lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma diabetic ketoacidosis diffuse large B-cell lymphoma embryoma endometrial cancer endometrial carcinoma enterobiasis esophagus squamous cell carcinoma granular cell carcinoma hepatitis B hepatocellular carcinoma intestinal schistosomiasis large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma middle cerebral artery infarction nasopharynx carcinoma neuroblastoma nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis sebaceous carcinoma skin melanoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma sweat gland cancer tongue squamous cell carcinoma trichinosis 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 uterine corpus cancer varicocele
2331	fibromodulin	FMOD Aliases: SLRR2E fibromodulin proteoglycan	Homo sapiens (human)	B-cell lymphoma Richter's syndrome adult cystic teratoma adult lymphoma adult teratoma age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer central nervous system lymphoma childhood leukemia childhood lymphoma chronic lymphocytic leukemia colon carcinoma colorectal cancer congestive heart failure coronary artery disease cystic teratoma degeneration of macula and posterior pole embryoma enthesopathy exostosis female stress incontinence fibromyalgia giant cell glioblastoma gingivitis glioblastoma gliosarcoma glomerulonephritis high grade glioma kidney disease leiomyoma leukemia liver cirrhosis lung small cell carcinoma lymphoma macular degeneration malignant teratoma mantle cell lymphoma mature teratoma mixed glioma myofibroma myopia neovascular inflammatory vitreoretinopathy nephritis nephrosis obsolete ymphosarcoma osteoarthritis periarthritis periodontitis prostate cancer prostate carcinoma prostate disease pyoureter tendinitis teratoma uterine fibroid
5716	proteasome 26S subunit, non-ATPase 10	PSMD10	Homo sapiens (human)	B-cell lymphoma T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult cystic teratoma adult teratoma autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma childhood testicular germ cell tumor cholangiocarcinoma cholesteatoma of middle ear cholesteatoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cystic teratoma dedifferentiated liposarcoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis ehrlichiosis embryoma embryonal cancer embryonal carcinoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial retinoblastoma follicular adenoma gastroenteritis germ cell and embryonal cancer germ cell cancer germinoma gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease inflammatory bowel disease influenza intrahepatic cholangiocarcinoma invasive ductal carcinoma islet cell tumor large intestine cancer liposarcoma liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma malignant teratoma mature teratoma melanoma microcystic adenoma mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction myopia nonpapillary renal cell carcinoma normal pressure hydrocephalus obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma pleomorphic liposarcoma polyp of middle ear prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma retinopathy of prematurity sarcomatoid renal cell carcinoma schizophrenia seminoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratoma testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thymic carcinoma thymoma tongue squamous cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine corpus cancer viral infectious disease visual epilepsy
8692	hyaluronidase 2	HYAL2 Aliases: LUCA2 LuCa-2 PH-20 homolog lysosomal hyaluronidase	Homo sapiens (human)	B-cell lymphoma acute chest syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma childhood lymphoma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma dysplastic nevus syndrome embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis gastroenteritis gliosarcoma granular cell carcinoma high grade glioma ileitis ileocolitis inflammatory bowel disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma lymphoma melanoma microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IX mucopolysaccharidosis VI mucopolysaccharidosis obsolete Matthew-Wood syndrome obsolete ymphosarcoma osteoarthritis primary pulmonary hypertension pulmonary hypertension reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma skin melanoma squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer
197322	acyl-CoA synthetase family member 3	ACSF3 Aliases: malonyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
1040	CDP-diacylglycerol synthase 1	CDS1 Aliases: phosphatidate cytidylyltransferase	Homo sapiens (human)	B-cell lymphoma appendicitis arachnoiditis bipolar disorder breast cancer cancer carcinoma carotid stenosis chondrosarcoma colorectal cancer colorectal carcinoma congestive heart failure depressive disorder diffuse large B-cell lymphoma embryoma exanthema subitum eye disease giant cell glioblastoma glioblastoma high grade glioma large intestine cancer meningitis milker's nodule myasthenia gravis obsolete ymphosarcoma panic disorder sarcomatoid carcinoma substance abuse substance-related disorder temporal arteritis variola major
89790	sialic acid binding Ig like lectin 10	SIGLEC10 Aliases: MGC126774 PRO940 SIGLEC-10 SLG2 sialic acid binding Ig-like lectin 10 Ig-like lectin 7 siglec-like gene 2	Homo sapiens (human)	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
1577	cytochrome P450 family 3 subfamily A member 5	CYP3A5 Aliases: CP35 P450PCN3 PCN3	Homo sapiens (human)	B-lymphoblastic leukemia/lymphoma Balkan nephropathy Cockayne syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia abdominal obesity-metabolic syndrome 1 acute biphenotypic leukemia acute chest syndrome acute intermittent porphyria acute leukemia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia adult medulloblastoma adult respiratory distress syndrome agnosia agranulocytosis alcohol dependence alcohol use disorder allergic asthma ankylosing spondylitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune lymphoproliferative syndrome bladder carcinoma bone disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cartilage disease central nervous system origin vertigo central sleep apnea cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood medulloblastoma cholestasis chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma clonorchiasis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure connective tissue disease coronary artery disease depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health embryoma end stage renal disease epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome familial periodic paralysis follicular adenoma gastrointestinal system cancer glomerulonephritis heart disease hepatitis C hepatocellular carcinoma hypertension immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leukemia leukopenia lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus nephritis lymphoblastic lymphoma lymphoid leukemia medulloblastoma medullomyoblastoma melanotic medulloblastoma membranous glomerulonephritis microcystic adenoma microphthalmia myasthenia gravis myelodysplastic syndrome myeloid leukemia myopathy nephritis nephrolithiasis nephrosclerosis nephrosis nephrotic syndrome neuroblastoma neuropathy neutropenia newborn respiratory distress syndrome nicotine dependence nodular prostate nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome oral submucous fibrosis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma papillary adenoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy pre-eclampsia prostate cancer prostate carcinoma prostatic adenoma psychotic disorder pyoureter renal carcinoma renal cell carcinoma renal hypertension rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seminoma severe congenital neutropenia squamous cell carcinoma subacute delirium systemic lupus erythematosus testicular cancer testicular malignant germ cell cancer testis seminoma thrombophilia thrombosis tongue squamous cell carcinoma toxic encephalopathy tuberculosis type 2 diabetes mellitus ulcerative colitis uric acid nephrolithiasis urinary bladder cancer
24842	tumor protein p53	Tp53	Rattus norvegicus (Norway rat)	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
22059	transformation related protein 53	Trp53	Mus musculus (house mouse)	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
7157	tumor protein p53	TP53	Homo sapiens (human)	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
1120	choline kinase beta	CHKB Aliases: CHETK	Homo sapiens (human)	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy agnosia 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder 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 distal myopathy epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder intellectual disability isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy nemaline myopathy 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 recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
3423	iduronate 2-sulfatase	IDS Aliases: Hunter syndrome ID2S	Homo sapiens (human)	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 Aliases: FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Homo sapiens (human)	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
1375	carnitine palmitoyltransferase 1B	CPT1B Aliases: CPT1-M M-CPT1 carnitine O-palmitoyltransferase 1B	Homo sapiens (human)	Balo concentric sclerosis Down syndrome Pearson syndrome acute myocardial infarction adrenoleukodystrophy bladder carcinoma cancer central nervous system disease chronic recurrent multifocal osteomyelitis colitis congestive heart failure coronary thrombosis embryoma gastroenteritis hepatitis hepatocellular carcinoma ileitis ileocolitis liver cancer morbid obesity myocardial infarction narcolepsy post-traumatic stress disorder restless legs syndrome silent myocardial infarction steatotic liver disease systemic primary carnitine deficiency disease urinary bladder cancer very long chain acyl-CoA dehydrogenase deficiency
411	arylsulfatase B	ARSB Aliases: ASB	Homo sapiens (human)	Balo concentric sclerosis Fabry disease Laron syndrome Machado-Joseph disease Scheie syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cardiomyopathy carotid artery disease central nervous system disease chondrodysplasia punctata chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis embryoma endomyocardial fibrosis essential hypertension glaucoma glycogen storage disease II hydrocephalus hypertension hypertrichosis hypertrophic cardiomyopathy inguinal hernia large intestine cancer lipid storage disease lung benign neoplasm lysosomal storage disease melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myocarditis narcolepsy nervous system disease obstructive hydrocephalus omphalocele osteochondrodysplasia osteonecrosis prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder senile degeneration of brain sensorineural hearing loss skin melanoma spinal cord disease tuberculosis umbilical hernia
2262	glypican 5	GPC5 Aliases: glypican proteoglycan 5	Homo sapiens (human)	Balo concentric sclerosis Gilles de la Tourette syndrome MHC class II deficiency Marfan syndrome Simpson-Golabi-Behmel syndrome type 1 adenosine deaminase deficiency adrenoleukodystrophy bronchus cancer bronchus carcinoma cancer cardiac arrest cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types central nervous system cancer central nervous system disease central nervous system lymphoma demyelinating disease diabetes mellitus epithelioid sarcoma familial nephrotic syndrome gliosarcoma glomerulonephritis hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma microphthalmia mixed glioma multiple sclerosis myelomeningocele narcolepsy nephritis nephrotic syndrome neuromyelitis optica obsolete Matthew-Wood syndrome obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma proteinuria rhabdomyosarcoma rheumatoid arthritis sarcoma scoliosis severe combined immunodeficiency situs inversus spina bifida spindle cell sarcoma tethered spinal cord syndrome tetralogy of Fallot transthyretin amyloidosis tuberous sclerosis type 2 diabetes mellitus
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
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
161357	MAM domain containing glycosylphosphatidylinositol anchor 2	MDGA2	Homo sapiens (human)	Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy benign epilepsy with centrotemporal spikes cancer central nervous system disease dissociative disorder embryoma microinvasive gastric cancer narcolepsy neurotic disorder rheumatoid arthritis sexual dysfunction stomach cancer stomach carcinoma systemic lupus erythematosus
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
9348	N-deacetylase and N-sulfotransferase 3	NDST3 Aliases: HSST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder autism spectrum disorder azoospermia central nervous system disease depressive disorder generalized anxiety disorder intellectual disability major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia
4245	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT1 Aliases: GLCNAC-TI GNT-1 GnTI	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease central nervous system cancer central nervous system disease complex partial epilepsy congestive heart failure cystinuria diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism embryoma endomyocardial fibrosis epilepsy galactokinase deficiency galactosemia gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycine encephalopathy glycogen storage disease Ia glycogen storage disease heart disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease liver cancer mixed glioma multiple sclerosis narcolepsy nervous system disease obesity obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder temporal lobe epilepsy 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 visual epilepsy
266722	heparan sulfate 6-O-sulfotransferase 3	HS6ST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer central nervous system disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy hepatitis B narcolepsy nicotine dependence obesity type 2 diabetes mellitus

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