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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 **1201 - 1225** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
176879	Putative sphingomyelin phosphodiesterase asm-3;Sphingomyelin phosphodiesterase	asm-3	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
181323	Sphingomyelin phosphodiesterase 2	asm-2	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
18145	NPC intracellular cholesterol transporter 1	Npc1	Mus musculus (house mouse)	Niemann-Pick disease type C1 Niemann-Pick disease
4864	NPC intracellular cholesterol transporter 1	NPC1 Aliases: SLC65A1	Homo sapiens (human)	Niemann-Pick disease type C1 Niemann-Pick disease
10924	sphingomyelin phosphodiesterase acid like 3A	SMPDL3A Aliases: ASM3A ASML3a FLJ20177 acid sphingomyelinase-like phosphodiesterase 3a yR36GH4.1	Homo sapiens (human)	Niemann-Pick disease endometriosis of ovary endometriosis of uterus endometriosis sphingolipidosis urinary bladder cancer
23423	transmembrane p24 trafficking protein 3	TMED3 Aliases: p24B p24g4 p24gamma4	Homo sapiens (human)	Nijmegen breakage syndrome anemia bacterial sepsis breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy fundus albipunctatus hepatocellular carcinoma large intestine cancer liver cancer macrocytic anemia nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma
856870	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	GLC7	Saccharomyces cerevisiae S288C	Noonan syndrome-like disorder with loose anagen hair 2 cancer congestive heart failure type 2 diabetes mellitus
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Rattus norvegicus (Norway rat)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Mus musculus (house mouse)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Xenopus tropicalis (tropical clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
443852	protein phosphatase 1, catalytic subunit, beta isozyme L homeolog	ppp1cb.L	Xenopus laevis (African clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2
108717671	protein phosphatase 1, catalytic subunit, beta isozyme S homeolog	ppp1cb.S	Xenopus laevis (African clawed frog)	Noonan syndrome-like disorder with loose anagen hair 2
90161	heparan sulfate 6-O-sulfotransferase 2	HS6ST2 Aliases: HS6ST-2	Homo sapiens (human)	Paganini-Miozzo syndrome arthritis arthropathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intellectual disability learning disability lung adenocarcinoma lung cancer myopia osteoarthritis stomach cancer stomach carcinoma
42380	Heparan sulfate 6-O-sulfotransferase	Hs6st	Drosophila melanogaster (fruit fly)	Paganini-Miozzo syndrome hypogonadotropic hypogonadism 15 with or without anosmia
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Mus musculus (house mouse)	Paganini-Miozzo syndrome
378450	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Danio rerio (zebrafish)	Paganini-Miozzo syndrome
302489	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Rattus norvegicus (Norway rat)	Paganini-Miozzo syndrome
100496603	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Xenopus tropicalis (tropical clawed frog)	Paganini-Miozzo syndrome
5287	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta	PIK3C2B Aliases: C2-PI3K PI3K-C2beta	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome adult acute lymphocytic leukemia breast cancer breast carcinoma cancer central nervous system cancer cerebral infarction cerebrovascular disease chronic lymphocytic leukemia esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma lung small cell carcinoma mixed glioma neuroblastoma prostate cancer prostate carcinoma scleroderma systemic scleroderma
6888	transaldolase 1	TALDO1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease carbohydrate metabolic disorder childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
127	alcohol dehydrogenase 4 (class II), pi polypeptide	ADH4 Aliases: ADH-2	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute myeloid leukemia acute pancreatitis adenocarcinoma adenoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis anaplastic astrocytoma cancer carcinoma childhood cerebral astrocytoma cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fibrillary astrocytoma flat ductal epithelial atypia gemistocytic astrocytoma granular cell carcinoma hepatitis C hepatocellular carcinoma high grade glioma invasive ductal carcinoma juvenile pilocytic astrocytoma liver cancer liver cirrhosis malignant astrocytoma migraine ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pharynx cancer pilocytic astrocytoma protoplasmic astrocytoma squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma
80351	tankyrase 2	TNKS2 Aliases: ARTD6 PARP-5b PARP-5c PARP5B PARP5C TANK2 TNKL TRF1-interacting ankyrin-related ADP-ribose polymerase 2 pART6	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma cleft lip cribriform carcinoma depressive disorder diabetes mellitus endometrial cancer endometrial carcinoma granular cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia osteosarcoma skin benign neoplasm skin cancer squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer
79993	ELOVL fatty acid elongase 7	ELOVL7 Aliases: FLJ23563	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy cancer hidradenitis suppurativa hidradenitis inflammatory bowel disease multiple system atrophy pompholyx prostate cancer prostate carcinoma
5279	phosphatidylinositol glycan anchor biosynthesis class C	PIGC Aliases: GPI2 PIG-C phosphatidylinositol N-acetylglucosaminyltransferase subunit C	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease agnosia cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy glycosylphosphatidylinositol biosynthesis defect 16 intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nicotine dependence obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy

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