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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 **351 - 375** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
10873	malic enzyme 3	ME3 Aliases: malate dehydrogenase (oxaloacetate-decarboxylating) (NADP(+))	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer idiopathic scoliosis pancreatic cancer pancreatic carcinoma
10329	ribitol xylosyltransferase 1	RXYLT1 Aliases: HP10481	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
152330	contactin 4	CNTN4 Aliases: BIG-2	Homo sapiens (human)	adrenal gland cancer alcohol dependence alcohol use disorder amyotrophic lateral sclerosis type 1 anorexia nervosa autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia autosomal recessive spinocerebellar ataxia 16 bilateral optic nerve hypoplasia bipolar disorder breast cancer breast carcinoma cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma disease of mental health duodenum cancer epilepsy essential hypertension gallbladder cancer gallbladder carcinoma heart cancer hypertension intellectual disability large intestine cancer learning disability obesity ovarian cancer ovarian carcinoma paraganglioma pheochromocytoma primary open angle glaucoma psychotic disorder schizophrenia small intestine cancer speech disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
1603	defender against cell death 1	DAD1	Homo sapiens (human)	Barrett's esophagus allergic asthma asthma cancer embryoma intrinsic asthma lung small cell carcinoma neuroendocrine carcinoma neuroendocrine tumor
147991	dpy-19 like C-mannosyltransferase 3	DPY19L3	Homo sapiens (human)	depressive disorder major depressive disorder melancholic depression obsolete melancholia
129530	lysozyme g1	LYG1 Aliases: LYGA1 SALW1939	Homo sapiens (human)	cancer
140578	chondrolectin	CHODL Aliases: FLJ12627 MT75 PRED12	Homo sapiens (human)	bronchus cancer bronchus carcinoma bulimia nervosa cancer idiopathic scoliosis lung cancer lung carcinoma lung non-small cell carcinoma progressive muscular atrophy spinal muscular atrophy
93010	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3GNT7 Aliases: beta3GnT7	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
2992	glycogenin 1	GYG1 Aliases: glycogenin glucosyltransferase	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Lafora disease cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system origin vertigo coronary artery disease cystinuria diabetes mellitus disease of metabolism endomyocardial fibrosis familial periodic paralysis galactosemia 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 XV glycogen storage disease hypertrophic cardiomyopathy myopathy sick sinus syndrome type 2 diabetes mellitus
64781	ceramide kinase	CERK Aliases: DKFZp434E0211 FLJ21430 FLJ23239 KIAA1646 LK4 dA59H18.2 dA59H18.3 hCERK	Homo sapiens (human)	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
166929	sphingomyelin synthase 2	SGMS2 Aliases: MGC26963 SMS2	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 Pick's disease Reye syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bacterial sepsis bone osteosarcoma breast cancer breast carcinoma calvarial doughnut lesions with bone fragility cancer central nervous system cancer cerebral degeneration colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease dental caries dentin caries depressive disorder dysthymic disorder embryoma gastroenteritis gliosarcoma high grade glioma ileitis ileocolitis large intestine cancer major depressive disorder melancholic depression mixed glioma neurotic disorder obesity obsolete melancholia osteoporosis osteosarcoma pulmonary emphysema scoliosis steatotic liver disease
23443	solute carrier family 35 member A3	SLC35A3 Aliases: UDP-N-acetylglucosamine transporter	Homo sapiens (human)	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
7367	UDP glucuronosyltransferase family 2 member B17	UGT2B17	Homo sapiens (human)	Barrett's esophagus Graves' disease Richter's syndrome adenocarcinoma adenoma age related macular degeneration ankylosing spondylitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole embryoma endometrial cancer endometrial carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma hematologic cancer hyperthyroidism kidney disease kidney failure large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma macular degeneration nasopharynx carcinoma nephritis nephrosis nodular prostate osteoporosis primary cutaneous amyloidosis prostate cancer prostate carcinoma prostatic adenoma pyoureter substance abuse substance-related disorder thyrotoxicosis tubular adenocarcinoma uterine corpus cancer
341392	acyl-CoA synthetase medium chain family member 4	ACSM4 Aliases: similar to olfactory specific medium-chain acyl CoA synthetase	Homo sapiens (human)
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
594	branched chain keto acid dehydrogenase E1 subunit beta	BCKDHB Aliases: 2-oxoisovalerate dehydrogenase subunit beta, mitochondrial maple syrup urine disease	Homo sapiens (human)	Alzheimer's disease 12 Kaposi's sarcoma acute pancreatitis androgen insensitivity syndrome brain edema cancer celiac disease embryoma epilepsy hepatitis B hepatocellular carcinoma hypoglycemia intellectual disability lactic acidosis learning disability liver cancer maple syrup urine disease pancreatic cancer pancreatic carcinoma pancreatitis premature menopause primary ovarian insufficiency systemic lupus erythematosus thyroid gland anaplastic carcinoma visual epilepsy
962	CD48 molecule	CD48 Aliases: BLAST SLAMF2 hCD48 mCD48	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Castleman disease Fanconi anemia complementation group A Fanconi anemia Kimura disease Lyme disease Perlman syndrome Sotos syndrome St. Louis encephalitis West Nile fever X-linked cone-rod dystrophy 1 Zika fever acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma allergic asthma aplastic anemia asthma atopic dermatitis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome brain cancer cancer celiac disease central nervous system cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma chronic fatigue syndrome cone-rod dystrophy dermatitis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of uterus endometriosis essential thrombocythemia gliosarcoma glomerulonephritis high grade glioma influenza intrinsic asthma kidney disease leukemia lupus erythematosus lymphoma mixed glioma multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome nephritis obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma pancytopenia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia shigellosis systemic lupus erythematosus tetralogy of Fallot tick-borne encephalitis 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 viral infectious disease
9415	fatty acid desaturase 2	FADS2 Aliases: D6D DES6 FADSD6 SLL0262 TU13 delta-6-desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease Fabry disease Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction age related macular degeneration alcohol use disorder allergic asthma alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic kidney disease chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy discrete subaortic stenosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypothyroidism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kwashiorkor large intestine cancer laryngeal squamous cell carcinoma lipid metabolism disorder lipid storage disease liver cancer lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression myocardial infarction myxedema nephritis nephrosis neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition psoriatic arthritis pyoureter rheumatoid arthritis schizophrenia silent myocardial infarction skin disease steatotic liver disease stomach cancer stomach carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vitiligo
2739	glyoxalase I	GLO1 Aliases: GLOD1 lactoylglutathione lyase	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 Graves' disease Guillain-Barre 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 Miller Fisher syndrome Pick's disease Reye syndrome Sjogren's syndrome Werner syndrome acute myocardial infarction adult fibrosarcoma anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autism spectrum disorder autistic disorder autosomal dominant cerebellar ataxia bipolar disorder bladder carcinoma bone disease breast cancer breast carcinoma cancer carcinoma carotid artery disease cartilage disease central nervous system cancer cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebrovascular disease clear cell adenocarcinoma clear cell renal cell carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital adrenal hyperplasia connective tissue disease coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dysthymic disorder embryoma end stage renal disease endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma essential hypertension familial mediterranean fever familial nephrotic syndrome fibrosarcoma fundus albipunctatus gallbladder disease generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperthyroidism inflammatory breast carcinoma keratoconjunctivitis sicca kidney cancer kidney disease large intestine cancer lipoid nephrosis liver cancer liver cirrhosis liver disease major depressive disorder malaria melancholic depression melanoma mevalonic aciduria mixed glioma mood disorder motor neuritis multiple myeloma multiple sclerosis myocardial infarction nephritis nephrosis nephrotic syndrome neuritis neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis pancreatic cancer pancreatic carcinoma panic disorder phobic disorder progeria prostate cancer prostate carcinoma pyoureter renal carcinoma renal cell carcinoma restless legs syndrome retinal disease retinitis pigmentosa retinitis sarcomatoid carcinoma schizophrenia silent myocardial infarction skin melanoma spinocerebellar ataxia type 1 stomach cancer stomach carcinoma subacute sclerosing panencephalitis synovial sarcoma systemic lupus erythematosus thyroid gland anaplastic carcinoma thyrotoxicosis 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 urinary bladder cancer uterine corpus cancer vascular disease visual epilepsy
6382	syndecan 1	SDC1 Aliases: CD138 SYND1 syndecan syndecan proteoglycan 1	Homo sapiens (human)	B-cell lymphoma Bannayan-Riley-Ruvalcaba syndrome Burkitt lymphoma Cowden syndrome Crohn's colitis Crohn's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma, nodular sclerosis Hodgkin's lymphoma IgG4-related disease Kaposi's sarcoma Kawasaki disease POEMS syndrome Richter's syndrome acquired hyperkeratosis acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adhesions of uterus adult fibrosarcoma adult liposarcoma adult medulloblastoma allergic contact dermatitis ameloblastoma amyloidosis antithrombin III deficiency aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bacterial sepsis basal cell carcinoma benign mesothelioma benign peritoneal mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma blood coagulation disease bone disease bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cartilage disease celiac disease central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood liposarcoma childhood medulloblastoma cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell adenocarcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common variable immunodeficiency common wart congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma dedifferentiated liposarcoma dermatitis dermoid cyst diabetes mellitus diabetic cataract diabetic retinopathy diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disseminated intravascular coagulation diverticulitis of colon embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma essential hypertension extramedullary plasmacytoma familial hyperlipidemia familial nephrotic syndrome fibrolamellar carcinoma fibrosarcoma follicular lymphoma gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gonorrhea granular cell carcinoma granular corneal dystrophy 2 hair follicle neoplasm head and neck squamous cell carcinoma heavy chain disease hematologic cancer hepatitis C hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunoglobulin alpha deficiency impotence inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza interstitial nephritis intrahepatic cholangiocarcinoma invasive ductal carcinoma keratoacanthoma kidney disease kidney failure large intestine cancer leukemia lipoid nephrosis liposarcoma liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malaria malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma mesenchymal cell neoplasm microphthalmia mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia multiple myeloma multiple sclerosis myelitis myocardial infarction myoepithelioma nasopharynx carcinoma nephritis nephrosis nephrotic syndrome neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuromyelitis optica obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete inherited blood coagulation disease obsolete ymphosarcoma optic neuritis osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma papilloma parapsoriasis peritoneal mesothelioma pilomatrixoma placenta cancer placental insufficiency plasma cell neoplasm plasmacytoma pleomorphic liposarcoma pneumonia polycythemia vera polyp of corpus uteri postinflammatory pulmonary fibrosis pre-eclampsia premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease primary sclerosing cholangitis proliferative diabetic retinopathy prostate cancer prostate carcinoma protein C deficiency protein S deficiency proteinuria psoriasis psychologic dyspareunia pulmonary fibrosis purpura fulminans pustulosis of palm and sole pyelitis pyelonephritis pyoureter refractory plasma cell neoplasm relapsing-remitting multiple sclerosis renal cell carcinoma renal infectious disease renal oncocytoma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma sclerosing cholangitis sebaceous carcinoma selective IgA deficiency disease silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma subacute sclerosing panencephalitis sweat gland cancer systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma transitional cell carcinoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia urinary bladder cancer uterine corpus cancer uterus leiomyosarcoma
3906	lactalbumin alpha	LALBA Aliases: HAMLET LYZG LYZL7 lactose synthase B lysozyme G	Homo sapiens (human)	breast cancer breast carcinoma cancer deficiency anemia embryoma eosinophilic esophagitis fibromyalgia gastroenteritis hypochromic anemia liver cirrhosis microcytic anemia milk allergy mitral valve stenosis multiple sclerosis myositis obesity polycystic ovary syndrome steatotic liver disease
23761	phosphatidylserine decarboxylase	PISD Aliases: PSDC dJ858B16.2	Homo sapiens (human)	Parkinson's disease cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma common wart embryoma microcephaly nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma retinal disease sarcomatoid renal cell carcinoma
1836	solute carrier family 26 member 2	SLC26A2 Aliases: DTDST diastrophic dysplasia sulfate transporter	Homo sapiens (human)	Baraitser-Winter syndrome Bartter disease Clostridium difficile colitis Conn's syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pendred Syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome achondrogenesis type IB achondroplasia adenocarcinoma adenoma arthritis arthropathy atelosteogenesis auditory system disease autosomal recessive osteopetrosis 7 benign mesothelioma brachydactyly branchiootic syndrome breast cancer cancer chondrodysplasia punctata cleft palate clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure cryptorchidism cystic lymphangioma diarrhea diastrophic dysplasia disease of metabolism dyshormonogenic goiter embryoma endometritis fibrosarcoma follicular adenoma inguinal hernia irritable bowel syndrome isolated cleft palate juvenile rheumatoid arthritis large intestine cancer laryngostenosis lingual-facial-buccal dyskinesia lung benign neoplasm lung cancer lung non-small cell carcinoma malignant mesothelioma mastitis microcystic adenoma movement disease mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia 4 multiple epiphyseal dysplasia neurocirculatory asthenia omphalocele orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis otosclerosis papillary adenoma placental insufficiency polyhydramnios primary hyperaldosteronism scoliosis sensorineural hearing loss spinal cord disease spondylolysis stomach cancer stomach carcinoma umbilical hernia
140687	glucosaminyl (N-acetyl) transferase family member 7	GCNT7 Aliases: dJ1153D9.2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
204219	ceramide synthase 3	CERS3 Aliases: MGC27091	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome Weill-Marchesani syndrome achondroplasia acrodermatitis alopecia anhidrosis atopic dermatitis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis dermatitis ectropion hypohidrosis ichthyosis keratitis keratoconjunctivitis keratosis follicularis mongolian spot nonepidermolytic palmoplantar keratoderma obsolete congenital ichthyosiform erythroderma palmoplantar keratosis pseudoxanthoma elasticum sensorineural hearing loss

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