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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 **391301 - 391325** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
94203	placental growth factor	Pgf	Rattus norvegicus (Norway rat)	Crohn's disease amyotrophic lateral sclerosis ankylosing spondylitis asthma brain ischemia breast cancer carotid artery disease congestive heart failure diabetic neuropathy diabetic retinopathy end stage renal disease epilepsy glioblastoma hypertension limited scleroderma liver cirrhosis lymphedema myocardial infarction obesity pancreatic endocrine carcinoma pre-eclampsia pulmonary hypertension pyelonephritis renal cell carcinoma rheumatoid arthritis sickle cell anemia status epilepticus systemic lupus erythematosus temporal lobe epilepsy
94192	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	Mus musculus (house mouse)	autoimmune disease of blood
94181	N-acetylneuraminic acid synthase (sialic acid synthase)	Nans	Mus musculus (house mouse)	spondyloepimetaphyseal dysplasia, Genevieve-type
94101	ORMDL sphingolipid biosynthesis regulator 1	ORMDL1	Homo sapiens (human)	allergic asthma asthma intrinsic asthma
94005	phosphatidylinositol glycan anchor biosynthesis class S	PIGS Aliases: GPI transamidase component PIG-S GPI transamidase subunit PIG-S	Homo sapiens (human)	breast cancer cancer congenital nystagmus developmental and epileptic encephalopathy 95 dissociated nystagmus embryoma epilepsy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gingival hypertrophy gingival overgrowth hepatocellular carcinoma liver cancer microcephaly omphalocele pathologic nystagmus spontaneous ocular nystagmus umbilical hernia visual epilepsy
93978	C-type lectin domain containing 6A	CLEC6A Aliases: dectin-2 hDECTIN-2	Homo sapiens (human)	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
93961	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5	B3galt5	Mus musculus (house mouse)	pancreatic cancer
93611	F-box protein 44	FBXO44 Aliases: FBG3 FBX30 Fbx44 Fbxo6a MGC14140	Homo sapiens (human)	polycystic ovary syndrome prostate cancer prostate carcinoma
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 Aliases: alpha2delta-4	Homo sapiens (human)	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
93432	maltase-glucoamylase 2 (putative)	MGAM2	Homo sapiens (human)
93210	post-GPI attachment to proteins phospholipase 3	PGAP3 Aliases: CAB2 MGC9753 PER1 PP1498 post-GPI attachment to proteins 3	Homo sapiens (human)	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 4 inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
93183	phosphatidylinositol glycan anchor biosynthesis class M	PIGM Aliases: DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	Homo sapiens (human)	Budd-Chiari syndrome epilepsy focal epilepsy paroxysmal nocturnal hemoglobinuria partial motor epilepsy portal hypertension portal vein thrombosis thrombophilia visual epilepsy
93010	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3GNT7 Aliases: beta3GnT7	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
92579	glucose-6-phosphatase catalytic subunit 3	G6PC3 Aliases: UGRP	Homo sapiens (human)	Crohn's colitis Crohn's disease Marfan syndrome Wiskott-Aldrich syndrome acute myeloid leukemia agranulocytosis androgen insensitivity syndrome anemia 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 bacterial sepsis bronchiectasis cancer cleft palate colitis congenital heart disease cryptorchidism cyclic hematopoiesis cystinuria embryoma essential thrombocythemia eunuchism galactosemia gastroenteritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hydronephrosis hypogonadism ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability isolated cleft palate learning disability leukopenia lymphopenia macrocytic anemia microcephaly mitral valve insufficiency mitral valve prolapse myelodysplastic syndrome neutropenia oculocutaneous albinism pancytopenia patent ductus arteriosus patent foramen ovale premature menopause primary immunodeficiency disease primary pulmonary hypertension pulmonary valve stenosis sensorineural hearing loss severe congenital neutropenia 4 severe congenital neutropenia situs inversus thrombocytopenia tuberous sclerosis ulcerative colitis varicose veins
92483	lactate dehydrogenase A like 6B	LDHAL6B Aliases: LDH6B LDHL	Homo sapiens (human)	breast cancer breast carcinoma disease of metabolism
92370	2-phosphoxylose phosphatase 1	PXYLP1 Aliases: FLJ23751	Homo sapiens (human)	myopia
92126	dermatan sulfate epimerase like	DSEL	Homo sapiens (human)	colorectal cancer colorectal carcinoma congenital diaphragmatic hernia diabetes mellitus hiatus hernia large intestine cancer microphthalmia type 2 diabetes mellitus
91949	component of oligomeric golgi complex 7	COG7	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
91869	RFT1 homolog	RFT1 Aliases: CDG1N congenital disorder of glycosylation 1N	Homo sapiens (human)	Crohn's colitis Crohn's disease Laron syndrome Unverricht-Lundborg syndrome West syndrome achondroplasia blepharospasm blindness blood coagulation disease cancer clubfoot congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis early myoclonic encephalopathy epilepsy focal hand dystonia hypertropia inflammatory bowel disease 1 inflammatory bowel disease mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy obsolete inherited blood coagulation disease ophthalmoplegia schizophrenia sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 type 2 diabetes mellitus ulcerative colitis visual epilepsy
91373	UDP-N-acetylglucosamine pyrophosphorylase 1 like 1	UAP1L1	Homo sapiens (human)	hepatocellular carcinoma liver cancer
91012	ceramide synthase 5	CERS5 Aliases: FLJ25304 MGC45411 Trh4	Homo sapiens (human)	cancer colon cancer colonic benign neoplasm colorectal cancer congestive heart failure embryoma essential hypertension hypertension large intestine cancer rectal benign neoplasm rectum adenocarcinoma rectum cancer
90673	protein phosphatase 1 regulatory subunit 3E	PPP1R3E	Homo sapiens (human)
90411	multiple coagulation factor deficiency 2, ER cargo receptor complex subunit	MCFD2 Aliases: F5F8D LMAN1IP SDNSF	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease embryoma factor V deficiency factor VII deficiency factor VIII deficiency hematopoietic system disease nutmeg liver obsolete inherited blood coagulation disease seminoma testicular cancer testicular germ cell cancer testis seminoma transient cerebral ischemia vertebrobasilar insufficiency vitamin K deficiency bleeding
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
89944	galactosidase beta 1 like 2	GLB1L2	Homo sapiens (human)	acute myeloid leukemia

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