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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 **7901 - 7925** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
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
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
284369	SIGLEC family like 1	SIGLECL1 Aliases: FLJ40235	Homo sapiens (human)
150094	salt inducible kinase 1	SIK1	Homo sapiens (human)
23235	salt inducible kinase 2	SIK2	Homo sapiens (human)
23387	SIK family kinase 3	SIK3	Homo sapiens (human)
64374	SIL1 nucleotide exchange factor	SIL1	Homo sapiens (human)
6493	SIM bHLH transcription factor 2	SIM2	Homo sapiens (human)
375484	SUMO interacting motifs containing 1	SIMC1	Homo sapiens (human)
25942	SIN3 transcription regulator family member A	SIN3A	Homo sapiens (human)
23309	SIN3 transcription regulator family member B	SIN3B	Homo sapiens (human)
6494	signal-induced proliferation-associated 1	SIPA1	Homo sapiens (human)
26037	signal induced proliferation associated 1 like 1	SIPA1L1	Homo sapiens (human)
57568	signal induced proliferation associated 1 like 2	SIPA1L2	Homo sapiens (human)
23094	signal induced proliferation associated 1 like 3	SIPA1L3	Homo sapiens (human)
140885	signal regulatory protein alpha	SIRPA	Homo sapiens (human)
10326	signal regulatory protein beta 1	SIRPB1	Homo sapiens (human)
284759	signal regulatory protein beta 2	SIRPB2	Homo sapiens (human)
128646	signal regulatory protein delta	SIRPD	Homo sapiens (human)
55423	signal regulatory protein gamma	SIRPG	Homo sapiens (human)
23411	sirtuin 1	SIRT1	Homo sapiens (human)

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