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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 **601 - 625** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
27294	dihydrodiol dehydrogenase	DHDH Aliases: HUM2DD trans-1,2-dihydrobenzene-1,2-diol dehydrogenase	Homo sapiens (human)	bronchus cancer bronchus carcinoma carcinoma childhood germ cell cancer embryonal cancer esophagus squamous cell carcinoma germ cell and embryonal cancer germ cell cancer germinoma hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
27255	contactin 6	CNTN6 Aliases: NB-3 neural adhesion molecule	Homo sapiens (human)	Gilles de la Tourette syndrome Hirschsprung's disease Parkinson's disease 2 acquired immunodeficiency syndrome adenoid cystic carcinoma alcohol dependence alcohol use disorder anorexia nervosa attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder breast cancer communicating hydrocephalus cone-rod dystrophy 2 cone-rod dystrophy differentiated thyroid gland carcinoma epilepsy hydrocephalus intellectual disability learning disability obstructive hydrocephalus ovarian carcinoma salivary gland adenoid cystic carcinoma schizophrenia senile degeneration of brain systemic lupus erythematosus
27248	endoplasmic reticulum lectin 1	ERLEC1 Aliases: CL25084 ERLECTIN XTP3-B XTP3TPB erlectin 1	Homo sapiens (human)	anorexia nervosa bronchus cancer bronchus carcinoma cancer cholestasis lung benign neoplasm lung cancer lung carcinoma spinal cord disease syringomyelia
27235	coenzyme Q2, polyprenyltransferase	COQ2	Homo sapiens (human)	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
27232	glycine N-methyltransferase	GNMT	Homo sapiens (human)	glycine N-methyltransferase deficiency hepatocellular carcinoma
27230	stress associated endoplasmic reticulum protein 1	SERP1	Homo sapiens (human)
27181	sialic acid binding Ig like lectin 8	SIGLEC8 Aliases: MGC59785 SAF2 SIGLEC-8 SIGLEC8L	Homo sapiens (human)	Hirschsprung's disease Loeffler syndrome allergic asthma anisakiasis asthma cancer chronic obstructive pulmonary disease colitis eosinophilic esophagitis eosinophilic gastritis eosinophilic gastroenteritis eosinophilic pneumonia gastritis gastroenteritis hypereosinophilic syndrome ileitis ileocolitis intrinsic asthma pneumonia pulmonary eosinophilia
27180	sialic acid binding Ig like lectin 9	SIGLEC9 Aliases: CD329	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis cancer carcinoma chikungunya chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma dengue hemorrhagic fever embryoma giant cell glioblastoma glioblastoma hepatitis high grade glioma intrinsic asthma large intestine cancer lung cancer lung non-small cell carcinoma melanoma pulmonary emphysema rheumatoid arthritis sarcomatoid carcinoma skin melanoma
27163	N-acylethanolamine acid amidase	NAAA	Homo sapiens (human)	Alagille syndrome 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 Burkitt lymphoma DiGeorge syndrome Glanzmann's thrombasthenia Goodpasture syndrome Hantavirus hemorrhagic fever with renal syndrome Henoch-Schoenlein purpura 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 Japanese encephalitis Marfan syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis abdominal obesity-metabolic syndrome 1 acrodermatitis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia adult respiratory distress syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis bacterial sepsis bladder carcinoma blood coagulation disease bone marrow cancer cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia colorectal cancer colorectal carcinoma coronary artery disease craniosynostosis dengue disease dermatitis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia granulomatosis with polyangiitis gray platelet syndrome heart disease hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma hypersensitivity vasculitis inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer leukopenia liver cancer liver cirrhosis macrocytic anemia myelodysplastic syndrome myeloproliferative neoplasm newborn respiratory distress syndrome nicotine dependence obesity obsolete inherited blood coagulation disease obsolete type 1 diabetes mellitus 9 osteoarthritis platelet-type bleeding disorder 10 platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pneumonia polyarteritis nodosa portal hypertension portal vein thrombosis primary pulmonary hypertension prostate cancer prostate carcinoma qualitative platelet defect situs inversus steatotic liver disease thalassemia thrombocytopenia thrombocytosis 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 urinary bladder cancer velocardiofacial syndrome viral infectious disease yellow fever
27159	chitinase acidic	CHIA Aliases: AMCase CHIT2 TSA1902 acidic mammalian chitinase	Homo sapiens (human)	Sjogren's syndrome allergic asthma allergic conjunctivitis allergic rhinitis asthma cryptococcosis dry eye syndrome eosinophilic esophagitis giant papillary conjunctivitis intrinsic asthma keratoconjunctivitis sicca silicosis sinusitis vasomotor rhinitis vernal conjunctivitis xerophthalmia
27124	inositol polyphosphate-5-phosphatase J	INPP5J Aliases: INPP5 PIPP	Homo sapiens (human)	breast cancer breast carcinoma cancer
27111	syndecan binding protein 2	SDCBP2 Aliases: SITAC18 ST-2 syntenin-2	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 cancer cerebral degeneration colorectal cancer colorectal carcinoma congestive heart failure diarrhea epidermodysplasia verruciformis large intestine cancer
27090	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4	ST6GALNAC4 Aliases: SIAT3C ST6GALNACIV	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome cancer thyroid gland follicular carcinoma
27087	beta-1,3-glucuronyltransferase 1	B3GAT1 Aliases: GlcAT-P HNK-1 NK-1 galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 glucuronosyltransferase P	Homo sapiens (human)	Alport syndrome 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 Clouston syndrome Down syndrome Ewing sarcoma Felty's syndrome Goodpasture syndrome HCL-V Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Takayasu's arteritis Wolff-Parkinson-White syndrome Zika fever acoustic neuroma acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute lymphoblastic leukemia adult acute lymphocytic leukemia aggressive NK-cell leukemia agnosia agranulocytosis allergic asthma anaplastic astrocytoma anxiety disorder arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome axonal neuropathy bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cartilage disease cataract 5 multiple types celiac disease cellular schwannoma cerebral cavernous malformation 1 cerebral degeneration cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chromophobe renal cell carcinoma chronic NK-cell lymphocytosis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complex regional pain syndrome congenital myasthenic syndrome connective tissue disease coronary artery disease critical illness polyneuropathy depressive disorder diabetic ketoacidosis disease of mental health dysthymic disorder embryoma encephalomyelitis epidermolysis bullosa epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exostosis fibrillary astrocytoma fibrous dysplasia gastroparesis gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma glycine encephalopathy granulomatosis with polyangiitis hairy cell leukemia hemophagocytic lymphohistiocytosis hepatitis C hepatitis D high grade glioma human immunodeficiency virus infectious disease hypersensitivity vasculitis hypertension idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza intrinsic asthma juvenile pilocytic astrocytoma keratoacanthoma large intestine cancer leukemia leukopenia lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphopenia major depressive disorder malaria malignant astrocytoma malignant peripheral nerve sheath tumor melancholic depression melanoma melanotic neurilemmoma meningoencephalitis metanephric adenoma mucocutaneous leishmaniasis multiple myeloma multiple sclerosis myasthenia gravis myeloid leukemia myeloproliferative disorder with eosinophilia neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea osteoarthritis papillary carcinoma papillary renal cell carcinoma papilloma periapical granuloma peripheral nervous system disease phobic disorder pilocytic astrocytoma plasma cell neoplasm pleomorphic adenoma plexiform schwannoma polyarteritis nodosa polyneuropathy polyradiculoneuropathy post-traumatic stress disorder postinflammatory pulmonary fibrosis primary biliary cholangitis primary sclerosing cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pulmonary fibrosis renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis severe congenital neutropenia skin melanoma speech-language disorder-1 spindle cell sarcoma squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer subependymal giant cell astrocytoma sudden infant death syndrome tongue squamous cell carcinoma 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 ulcerative colitis uveal melanoma viral infectious disease
27076	LY6/PLAUR domain containing 3	LYPD3 Aliases: C4.4A	Homo sapiens (human)	cancer embryoma lung cancer lung non-small cell carcinoma squamous cell carcinoma tongue squamous cell carcinoma
27036	sialic acid binding Ig like lectin 7	SIGLEC7 Aliases: CD328 QA79 SIGLEC-7 p75/AIRM1	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 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 Marfan syndrome Miller Fisher syndrome 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 Zollinger-Ellison syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenosquamous carcinoma adult fibrosarcoma adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis alternating hemiplegia of childhood amyotrophic lateral sclerosis ankylosing spondylitis arthritis arthropathy atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autonomic neuropathy autosomal dominant familial periodic fever benign mesothelioma bipolar disorder bone marrow cancer brain stem infarction breast cancer breast carcinoma cancer cellular schwannoma central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood medulloblastoma chordoma chronic lymphocytic leukemia chronic monocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy delusional disorder depressive disorder dermatitis detrusor sphincter dyssynergia diabetes mellitus diabetic ketoacidosis dysthymic disorder eating disorder embryoma endometriosis of uterus endometriosis epilepsy esophagus squamous cell carcinoma familial combined hyperlipidemia familial hypercholesterolemia familial retinoblastoma fibrosarcoma gallbladder disease gangliocytoma ganglioneuroblastoma ganglioneuroma gastrinoma gastrointestinal system cancer gliosarcoma glomerulonephritis hepatitis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperglycemia hyperinsulinism kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver disease lymphoid leukemia major depressive disorder malignant mesothelioma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma melanotic neurilemmoma microphthalmia mixed glioma motor peripheral neuropathy myeloid leukemia myeloproliferative neoplasm nephritis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurotic disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia osteoarthritis pancreatic ductal adenocarcinoma panic disorder paranoid schizophrenia plexiform schwannoma preretinal fibrosis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma retinoblastoma rheumatoid arthritis rhinitis sick sinus syndrome situs inversus skin melanoma squamous cell carcinoma steatotic liver disease supratentorial primitive neuroectodermal tumor tendinitis tongue squamous cell carcinoma trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus vasomotor rhinitis
26503	solute carrier family 17 member 5	SLC17A5 Aliases: AST ISSD NSD SD SIALIN SLD Salla disease acidic sugar transporter infantile sialic acid storage disorder	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Crimean-Congo hemorrhagic fever Gilbert syndrome HELLP syndrome IgA glomerulonephritis Japanese encephalitis Lassa fever Parkinson's disease Plasmodium falciparum malaria Reye syndrome Stevens-Johnson syndrome Wilson disease abdominal obesity-metabolic syndrome 1 acrodermatitis acute pancreatitis adrenoleukodystrophy agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma alternating exotropia amelogenesis imperfecta type 1E amnestic disorder amyotrophic lateral sclerosis type 1 anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hepatitis autoimmune polyendocrine syndrome bilirubin metabolic disorder cancer cardiovascular system disease cataract 2 multiple types cataract 30 cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chromosome 17p13.1 deletion syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common cold communicating hydrocephalus congenital nystagmus congenital ptosis congestive heart failure coronary artery disease dementia dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism disseminated intravascular coagulation dissociated nystagmus dysthymic disorder embryoma epilepsy essential hypertension essential thrombocythemia exotropia familial hyperlipidemia familial nephrotic syndrome fascioliasis fibromyalgia gallbladder disease gingival hypertrophy gingival overgrowth glomerulonephritis glucose intolerance glycogen storage disease II head and neck squamous cell carcinoma heart disease hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hyperglycemia hypertension hypohidrotic ectodermal dysplasia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome intellectual disability intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy leukopenia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung cancer lung non-small cell carcinoma lymphopenia lysosomal storage disease macrocytic anemia major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma microphthalmia monocular exotropia myelodysplastic syndrome myocarditis myositis narcolepsy nasopharyngitis nephritis nephrosis nephrotic syndrome neurodegenerative disease neurotic disorder neutropenia obesity obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteoarthritis osteomalacia pancreatitis pancytopenia parapsoriasis pathologic nystagmus pneumonia portal vein thrombosis pre-eclampsia prediabetes syndrome primary polycythemia primary sclerosing cholangitis psoriasis ptosis purpura fulminans pustulosis of palm and sole pyoureter retrograde amnesia rheumatoid arthritis rickets sclerosing cholangitis senile degeneration of brain severe congenital neutropenia sialuria sickle cell anemia skin melanoma spontaneous ocular nystagmus steatotic liver disease subcortical band heterotopia thrombocytopenia tuberculosis type 2 diabetes mellitus uremia viral infectious disease visceral leishmaniasis visual epilepsy yellow fever
26330	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	GAPDHS Aliases: GAPD2 GAPDH-2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Pick's disease Reye syndrome cancer cerebral degeneration diabetes mellitus diabetic ketoacidosis embryoma melanoma skin melanoma
26301	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)	GBGT1 Aliases: A3GALNT FS Forssman blood group Forssman glycolipid synthetase (FS) Forssman synthetase MGC44848 UDP-GalNAc	Homo sapiens (human)	cancer celiac disease embryoma ovarian cancer ovarian carcinoma thrombophilia
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 Aliases: GALNAC-T8 polypeptide GalNAc transferase 8	Homo sapiens (human)	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
26280	interleukin 1 receptor accessory protein like 2	IL1RAPL2 Aliases: IL-1R9 IL1R9 IL1RAPL-2 TIGIRR-1	Homo sapiens (human)	autism spectrum disorder autistic disorder breast cancer childhood type dermatomyositis dermatomyositis hepatitis C myositis
26279	phospholipase A2 group IID	PLA2G2D Aliases: sPLA2S	Homo sapiens (human)	Down syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascending cholangitis atherosclerosis breast cancer cancer cholangitis chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease embryoma large intestine cancer primary sclerosing cholangitis sclerosing cholangitis suppurative cholangitis
26275	3-hydroxyisobutyryl-CoA hydrolase	HIBCH	Homo sapiens (human)	Leigh disease Unverricht-Lundborg syndrome West syndrome agnosia arthritis arthropathy blepharospasm brain disease cancer colorectal cancer colorectal carcinoma congenital nystagmus cryptorchidism developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy epilepsy focal hand dystonia generalized dystonia hydrocephalus hypertropia inherited metabolic disorder lactic acidosis large intestine cancer mechanical strabismus neurodegenerative disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus spontaneous ocular nystagmus strabismus tetralogy of Fallot 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

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