GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1376 - 1400** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
6402	selectin L	SELL Aliases: CD62L LAM-1 LAM1 LSEL Leu-8 Lyam-1 PLNHR hLHRc	Homo sapiens (human)	Alzheimer's disease B-cell lymphoma Behcet's disease Burkitt lymphoma Clostridium difficile colitis Crohn's colitis Crohn's disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma IgA glomerulonephritis Langerhans-cell histiocytosis Richter's syndrome Sezary's disease St. Louis encephalitis T-cell acute lymphoblastic leukemia abdominal aortic aneurysm acquired immunodeficiency syndrome acute chest syndrome acute myeloid leukemia acute myocardial infarction acute pancreatitis adenoma adult T-cell leukemia/lymphoma adult-onset Still's disease age related macular degeneration allergic asthma anthracosilicosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bladder carcinoma brain cancer brucellosis bullous pemphigoid cancer celiac disease cerebral infarction cerebrovascular disease childhood leukemia chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic angiopathy diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma disseminated intravascular coagulation duodenal ulcer embryoma end stage renal disease endometriosis of uterus endometriosis enthesopathy epidermolysis bullosa acquisita essential hypertension extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue fibromyalgia follicular adenoma gastric lymphoma gastritis gastroenteritis glomerulonephritis graft-versus-host disease head and neck squamous cell carcinoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma human immunodeficiency virus infectious disease hypereosinophilic syndrome hypertension hyperthyroidism ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma ischemia keratosis follicularis kidney disease kidney failure large intestine cancer leishmaniasis leukemia leukopenia liver cancer lymphangioleiomyomatosis lymphocytic choriomeningitis lymphoma macular degeneration melanoma melioidosis microcystic adenoma migraine mongolian spot multiple myeloma mycosis fungoides myocardial infarction nephritis nephrosis neuroendocrine carcinoma non-Hodgkin lymphoma nutmeg liver obsolete T-cell lymphoblastic leukemia/lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma pancreatic adenocarcinoma pancreatitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paroxysmal nocturnal hemoglobinuria perinatal necrotizing enterocolitis periodontal disease periodontitis peripheral vascular disease pneumonia pre-eclampsia primary cutaneous T-cell non-Hodgkin lymphoma pseudoxanthoma elasticum psoriatic arthritis pulmonary tuberculosis purpura fulminans pyoureter reticulosarcoma rheumatoid arthritis schizophrenia scleroderma sickle cell anemia silent myocardial infarction silicosis skin melanoma steatotic liver disease stomach cancer systemic lupus erythematosus systemic scleroderma thyroid gland papillary carcinoma thyroiditis thyrotoxicosis toxic shock syndrome transient cerebral ischemia tropical spastic paraparesis tuberculosis tuberculous pneumothorax 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 uremia urinary bladder cancer vascular disease vertebrobasilar insufficiency visceral leishmaniasis
6403	selectin P	SELP Aliases: CD62 CD62P GMP140 PADGEM PSEL antigen CD62 granule membrane protein 140kDa	Homo sapiens (human)	Alzheimer's disease Burkitt lymphoma Evans' syndrome Gilbert syndrome Glanzmann's thrombasthenia Goodpasture syndrome Kawasaki disease Proteus syndrome Sjogren's syndrome St. Louis encephalitis Takayasu's arteritis Zika fever abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute chest syndrome acute myocardial infarction acute necrotizing pancreatitis age related macular degeneration agranulocytosis allergic asthma ankylosing spondylitis anti-basement membrane glomerulonephritis antiphospholipid syndrome antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura bacterial sepsis beta thalassemia bilirubin metabolic disorder blood coagulation disease brain small vessel disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon carcinoma colorectal cancer common cold congenital heart disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis cystic fibrosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dysthymic disorder embryoma encephalitis encephalomyelitis epithelioid sarcoma essential hypertension essential thrombocythemia familial combined hyperlipidemia familial hyperlipidemia focal segmental glomerulosclerosis gallbladder disease gastroenteritis gastrointestinal stromal tumor giant cell glioblastoma glioblastoma glomerulonephritis granulomatosis with polyangiitis gray platelet syndrome head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hypoglycemia ileitis ileocolitis immune system disease intermediate coronary syndrome intrinsic asthma juvenile rheumatoid arthritis keratosis follicularis kidney disease kidney failure kwashiorkor leukopenia liver cancer liver carcinoma liver disease lung adenocarcinoma lung cancer lung carcinoma lupus erythematosus macular degeneration major depressive disorder marasmus melancholic depression mongolian spot multiple myeloma multiple sclerosis myelitis myelofibrosis myocardial infarction myotonic dystrophy type 1 myotonic dystrophy type 2 nasopharyngitis nasopharynx carcinoma nephritis neuroblastoma neurotic disorder neutropenia nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma parapsoriasis peripheral artery disease platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pneumonia polyarteritis nodosa portal vein thrombosis primary pulmonary hypertension proliferative diabetic retinopathy protein C deficiency protein S deficiency protein-energy malnutrition pseudoxanthoma elasticum psoriasis pulmonary embolism pustulosis of palm and sole qualitative platelet defect renal carcinoma renal cell carcinoma rheumatoid arthritis sarcoma sarcomatoid renal cell carcinoma severe congenital neutropenia sick sinus syndrome sickle cell anemia silent myocardial infarction spindle cell sarcoma systemic lupus erythematosus thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia transient cerebral ischemia 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 vertebrobasilar insufficiency von Willebrand's disease 3 von Willebrand's disease
85465	selenoprotein I	SELENOI Aliases: KIAA1724 SELI SEPI	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cleft palate coronary artery disease hepatoblastoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 81 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia isolated cleft palate liver cancer microcephaly
8482	semaphorin 7A (JohnMiltonHagen blood group)	SEMA7A Aliases: CD108 H-Sema K1 H-Sema-L John Milton Hagen blood group	Homo sapiens (human)	Kallmann syndrome Kaposi's sarcoma Sheehan syndrome Sjogren's syndrome St. Louis encephalitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy autosomal dominant polycystic kidney disease breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system disease cerebral infarction cerebrovascular disease chronic fatigue syndrome complex partial epilepsy congenital myasthenic syndrome coronary artery disease embryoma encephalitis encephalomyelitis epilepsy essential hypertension eunuchism gliosarcoma high grade glioma hypertension hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoconjunctivitis sicca lung adenocarcinoma lung cancer melanoma mixed glioma multiple sclerosis myelitis nervous system disease pancreatic cancer pancreatic carcinoma panhypopituitarism pneumonia polycystic kidney disease 1 postinflammatory pulmonary fibrosis progressive familial intrahepatic cholestasis pterygium pulmonary fibrosis rheumatoid arthritis septooptic dysplasia skin melanoma systemic lupus erythematosus temporal lobe epilepsy visual epilepsy
5552	serglycin	SRGN Aliases: PPG serglycin proteoglycan	Homo sapiens (human)	MHC class II deficiency Sertoli cell-only syndrome Y-linked spermatogenic failure 1 acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adult respiratory distress syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer childhood type dermatomyositis cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis degenerative disc disease dental caries dentin caries dermatomyositis diabetes mellitus diabetic cataract diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health embryoma enterocele esophagus squamous cell carcinoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance gynecomastia hepatitis B hepatocellular carcinoma high grade glioma hypertension infant gynecomastia isolated cleft palate large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus male infertility malignant pleural mesothelioma mixed glioma multiple myeloma nasopharynx carcinoma newborn respiratory distress syndrome nutmeg liver oligospermia oral candidiasis osteoarthritis prediabetes syndrome psychotic disorder sarcomatoid carcinoma severe combined immunodeficiency type 2 diabetes mellitus
10993	serine dehydratase	SDS	Homo sapiens (human)
6470	serine hydroxymethyltransferase 1	SHMT1 Aliases: 14 kDa protein MGC15229 MGC24556 SHMT cSHMT cytoplasmic serine hydroxymethyltransferase	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Down syndrome Langerhans-cell histiocytosis Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia alcohol use disorder alopecia alternating hemiplegia of childhood autistic disorder autonomic neuropathy bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma embryoma epilepsy esophagus squamous cell carcinoma essential hypertension follicular adenoma gastric cardia adenocarcinoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hyperhomocysteinemia hyperphosphatemia hypertension intestinal benign neoplasm intestinal cancer large intestine cancer laryngeal benign neoplasm laryngeal disease larynx cancer leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma microcystic adenoma multiple sclerosis nephroblastoma nervous system disease non-Hodgkin lymphoma obsolete ymphosarcoma optic papillitis ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma papilledema prostate cancer prostate carcinoma reticulosarcoma retinal edema sarcomatoid carcinoma schizophrenia situs inversus squamous cell carcinoma temporal arteritis thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease tuberous sclerosis tubular adenocarcinoma urinary bladder cancer
6472	serine hydroxymethyltransferase 2	SHMT2 Aliases: mSHMT mitochondrial serine hydroxymethyltransferase	Homo sapiens (human)	B-cell lymphoma Down syndrome Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease alcohol use disorder anemia arthritis arthropathy autistic disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastrointestinal system cancer gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intrahepatic cholangiocarcinoma large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia mixed glioma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteoarthritis prostate cancer prostate carcinoma reticulosarcoma schizophrenia stomach cancer stomach carcinoma
10558	serine palmitoyltransferase long chain base subunit 1	SPTLC1 Aliases: HSAN1 LCB1 SPTI hLCB1	Homo sapiens (human)	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 Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Riley-Day syndrome acquired hyperkeratosis agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood autonomic neuropathy bipolar disorder brain cancer breast cancer cancer central nervous system cancer central nervous system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma dementia diabetes mellitus disease of mental health embryoma frontotemporal dementia gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 2 hereditary sensory and autonomic neuropathy type 5 hereditary sensory neuropathy type 4 hereditary sensory neuropathy high grade glioma juvenile amyotrophic lateral sclerosis type 27 keratosis mixed glioma motor peripheral neuropathy nervous system disease neurodegenerative disease neuropathy nonpapillary renal cell carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum papillary renal cell carcinoma peripheral nervous system disease polyneuropathy psychotic disorder renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss sensory peripheral neuropathy skin disease type 2 diabetes mellitus
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	Homo sapiens (human)	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 acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
171546	serine palmitoyltransferase small subunit A	SPTSSA Aliases: small subunit of serine palmitoyltransferase A ssSPTa	Homo sapiens (human)	hereditary spastic paraplegia 90A hereditary spastic paraplegia 90B
165679	serine palmitoyltransferase small subunit B	SPTSSB Aliases: ADMP androgen down regulated in mouse prostate small subunit of serine palmitoyltransferase B ssSPTb	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease
10942	serine protease 21	PRSS21 Aliases: ESP-1 TEST1 testisin	Homo sapiens (human)	Behcet's disease Down syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder atrial fibrillation cancer cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer diabetes mellitus diabetic ketoacidosis disorder of sexual development embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatitis B hermaphroditism human immunodeficiency virus infectious disease monoclonal gammopathy of uncertain significance monoclonal paraproteinemia ovarian cancer ovarian carcinoma plasma cell neoplasm pseudohermaphroditism type 2 diabetes mellitus
360226	serine protease 41	PRSS41	Homo sapiens (human)	ovarian cancer ovarian carcinoma
5652	serine protease 8	PRSS8 Aliases: CAP1 channel-activating serine protease 1 prostasin	Homo sapiens (human)	Bartter disease Conn's syndrome Waterhouse-Friderichsen syndrome actinic keratosis alopecia autosomal recessive congenital ichthyosis 4B bladder carcinoma bladder urothelial carcinoma breast cancer breast carcinoma cancer central nervous system cancer cholera chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagus squamous cell carcinoma essential hypertension gastroenteritis gliosarcoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis influenza intestinal benign neoplasm intestinal cancer liver cancer lung cancer lung non-small cell carcinoma mixed glioma obsolete congenital ichthyosiform erythroderma ovarian cancer ovarian carcinoma oxyphilic adenoma papillary renal cell carcinoma placenta disease primary hyperaldosteronism prostate cancer prostate carcinoma in situ prostate carcinoma renal carcinoma renal cell carcinoma renal oncocytoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease tarsal-carpal coalition syndrome type 2 diabetes mellitus urinary bladder cancer
83931	serine/threonine kinase 40	STK40	Homo sapiens (human)
145264	serpin family A member 12	SERPINA12	Homo sapiens (human)	alpha 1-antitrypsin deficiency obesity type 2 diabetes mellitus
54414	sialic acid acetylesterase	SIAE	Homo sapiens (human)	autoimmune disease
6614	sialic acid binding Ig like lectin 1	SIGLEC1 Aliases: CD169 FLJ00051 FLJ00055 FLJ00073 FLJ32150 SIGLEC-1 dJ1009E24.1 sialoadhesin	Homo sapiens (human)	Ebola hemorrhagic fever Graves' disease Kaposi's sarcoma Marfan syndrome St. Louis encephalitis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bladder carcinoma breast cancer breast carcinoma cancer childhood leukemia chronic fatigue syndrome colitis common cold congenital heart block coronary artery disease diabetes mellitus embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma gastroenteritis glomerulonephritis head and neck squamous cell carcinoma hepatitis B hepatitis C hyperthyroidism ileitis ileocolitis immune system disease influenza intrinsic asthma kidney disease leukemia liver cirrhosis lupus erythematosus macrocytic anemia melanoma multiple myeloma multiple sclerosis myelitis nephritis nephrosis nutmeg liver prostate cancer prostate carcinoma pulmonary tuberculosis pyoureter respiratory syncytial virus infectious disease rheumatoid arthritis scleroderma situs inversus skin melanoma steatotic liver disease systemic lupus erythematosus systemic scleroderma thyrotoxicosis tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer viral infectious disease
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
114132	sialic acid binding Ig like lectin 11	SIGLEC11	Homo sapiens (human)
89858	sialic acid binding Ig like lectin 12	SIGLEC12 Aliases: S2V SLG Siglec-12 Siglec-L1 Siglec-XII	Homo sapiens (human)	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus
284266	sialic acid binding Ig like lectin 15	SIGLEC15 Aliases: HsT1361	Homo sapiens (human)	cancer embryoma osteoporosis
8778	sialic acid binding Ig like lectin 5	SIGLEC5 Aliases: CD170 OB-BP2 SIGLEC-5	Homo sapiens (human)	acute myeloid leukemia acute pericementitis aggressive periodontitis cancer diabetes mellitus diabetic ketoacidosis leprosy periodontitis periodontosis systemic lupus erythematosus type 2 diabetes mellitus

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