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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	October 29, 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 **8351 - 8375** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
6462	sex hormone binding globulin	SHBG	Homo sapiens (human)
503542	shadow of prion protein	SPRN	Homo sapiens (human)
51246	shisa family member 5	SHISA5	Homo sapiens (human)
388336	shisa family member 6	SHISA6	Homo sapiens (human)
729956	shisa family member 7	SHISA7	Homo sapiens (human)
440829	shisa family member 8	SHISA8	Homo sapiens (human)
729993	shisa family member 9	SHISA9	Homo sapiens (human)
85352	shisa like 1	SHISAL1	Homo sapiens (human)
100132916	shisa like 2B	SHISAL2B	Homo sapiens (human)
57698	shootin 1	SHTN1	Homo sapiens (human)
195814	short chain dehydrogenase/reductase family 16C member 5	SDR16C5	Homo sapiens (human)
121214	short chain dehydrogenase/reductase family 9C member 7	SDR9C7	Homo sapiens (human)
57619	shroom family member 3	SHROOM3	Homo sapiens (human)
57477	shroom family member 4	SHROOM4	Homo sapiens (human)
6477	siah E3 ubiquitin protein ligase 1	SIAH1	Homo sapiens (human)
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
100049587	sialic acid binding Ig like lectin 14	SIGLEC14	Homo sapiens (human)
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
946	sialic acid binding Ig like lectin 6	SIGLEC6 Aliases: CD327 OB-BP1 SIGLEC-6	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia colorectal cancer colorectal carcinoma large intestine cancer subacute bacterial endocarditis systemic lupus erythematosus
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

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