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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 **1401 - 1425** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
6518	solute carrier family 2 member 5	SLC2A5	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myeloid leukemia breast cancer breast carcinoma cancer central nervous system cancer childhood B-cell acute lymphoblastic leukemia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetes mellitus disease of metabolism embryoma essential hypertension gliosarcoma hepatocellular carcinoma high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease intestinal atresia large intestine cancer liver cancer long QT syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity ovarian cancer ovarian carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma tropical sprue type 2 diabetes mellitus
3957	galectin 2	LGALS2 Aliases: HL14	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myocardial infarction amyotrophic lateral sclerosis angiostrongyliasis arteriosclerotic cardiovascular disease atherosclerosis cancer cardiovascular system disease cerebral infarction cerebral malaria cerebrovascular disease colitis coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis essential hypertension filariasis gastroenteritis heart disease hypertension ileitis ileocolitis inflammatory bowel disease myocardial infarction nutmeg liver perinatal necrotizing enterocolitis placental insufficiency progressive muscular atrophy rheumatoid arthritis silent myocardial infarction stomach cancer stomach carcinoma
2180	acyl-CoA synthetase long chain family member 1	ACSL1 Aliases: ACS1 FACL1 LACS LACS1 LACS2 lignoceroyl-CoA synthase long-chain fatty-acid-coenzyme A ligase 1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bacterial sepsis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cervix uteri carcinoma in situ chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy endomyocardial fibrosis gliosarcoma glomerulonephritis glucose metabolism disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease kidney disease large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma mixed glioma myocardial infarction nephritis nephrosis nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 papillary renal cell carcinoma pyoureter renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction steatotic liver disease 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 vascular disease
79143	membrane bound O-acyltransferase domain containing 7	MBOAT7 Aliases: BB1 LPIAT1 LPLAT LPLAT11 hMBOA-7 lysophosphatidylinositol acyltransferase lysophosphatidylinositol acyltransferase 1 lysophospholipid acyltransferase 11 lysophospholipid acyltransferase 7	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autosomal recessive intellectual developmental disorder 57 cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
5106	phosphoenolpyruvate carboxykinase 2, mitochondrial	PCK2 Aliases: PEPCK PEPCK2	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 bone osteosarcoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma hepatitis C hepatocellular carcinoma hyperglycemia hypoglycemia kwashiorkor liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus melanoma nutrition disease obesity osteosarcoma prostate cancer prostate carcinoma protein-energy malnutrition pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer skin melanoma steatotic liver disease type 2 diabetes mellitus viral infectious disease
2651	glucosaminyl (N-acetyl) transferase 2 (I blood group)	GCNT2 Aliases: IGNT Ii blood group NAGCT1 ULG3 bA360O19.2 bA421M1.1 unassigned linkage group 3	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma esophagus squamous cell carcinoma gallbladder cancer gallbladder carcinoma hyperferritinemia-cataract syndrome kidney failure large intestine cancer melanoma skin melanoma tuberculosis uremia
116285	acyl-CoA synthetase medium chain family member 1	ACSM1 Aliases: MACS1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 carcinoma cerebral palsy depressive disorder essential hypertension hemiplegia hypertension idiopathic scoliosis lung benign neoplasm lung carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia sarcomatoid carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
72774	nei endonuclease VIII-like 1 (E. coli)	Neil1	Mus musculus (house mouse)	abdominal obesity-metabolic syndrome obesity
9254	calcium voltage-gated channel auxiliary subunit alpha2delta 2	CACNA2D2 Aliases: KIAA0558 alpha2delta-2 gene 26	Homo sapiens (human)	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
1632	enoyl-CoA delta isomerase 1	ECI1 Aliases: 3,2 trans-enoyl-CoA isomerase	Homo sapiens (human)	achalasia carcinoma congenital diaphragmatic hernia dilated cardiomyopathy 1A dilated cardiomyopathy esophagitis gastroesophageal reflux disease hiatus hernia megaesophagus peptic esophagitis
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
10232	mesothelin	MSLN Aliases: CAK1 MPF	Homo sapiens (human)	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma common bile duct neoplasm cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreas disease pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
25976	TCDD inducible poly(ADP-ribose) polymerase	TIPARP Aliases: ARTD14 DDF1 DKFZP434J214 DKFZp686N0351 PARP-1 PARP-7 PARP7 RM1 pART14	Homo sapiens (human)	acoustic neuroma alcohol dependence alcohol use disorder angiomatous meningioma benign meningioma cancer cerebral convexity meningioma cervical cancer cervix carcinoma clear cell meningioma embryoma fibrous meningioma hepatitis A hepatitis intraorbital meningioma intraventricular meningioma meningioma meningothelial meningioma microcystic meningioma olfactory groove meningioma ovarian cancer parasagittal meningioma pituitary adenoma psammomatous meningioma secretory meningioma spinal meningioma transitional meningioma
7512	X-prolyl aminopeptidase 2	XPNPEP2	Homo sapiens (human)	acquired angioedema androgen insensitivity syndrome angioedema cancer cervical adenocarcinoma cervical cancer cervix carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hereditary angioedema nonpapillary renal cell carcinoma papillary renal cell carcinoma premature menopause primary cutaneous amyloidosis primary ovarian insufficiency prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
84803	glycerol-3-phosphate acyltransferase 3	GPAT3 Aliases: AGPAT10 HMFN0839 LPAAT-theta MAG1 MGC11324 lysophosphatidic acid acyltransferase, theta	Homo sapiens (human)	acquired immunodeficiency syndrome acute myeloid leukemia breast cancer cancer endometritis human immunodeficiency virus infectious disease leech infestation myiasis obesity toxoplasmosis
2592	galactose-1-phosphate uridylyltransferase	GALT	Homo sapiens (human)	acquired immunodeficiency syndrome agnosia androgen insensitivity syndrome bacterial sepsis blood coagulation disease cancer cataract cerebellar ataxia cerebellar disease classic galactosemia cystinuria diabetic cataract diarrhea disease of metabolism endometriosis of uterus endometriosis galactokinase deficiency galactose epimerase deficiency galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma human immunodeficiency virus infectious disease hypoglycemia hypogonadism inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis learning disability liver cancer liver cirrhosis liver disease marasmus neonatal jaundice nutrition disease osteoporosis ovarian cancer ovarian carcinoma premature menopause primary ovarian insufficiency protein-energy malnutrition proteinuria speech-language disorder-1 trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
9162	diacylglycerol kinase iota	DGKI Aliases: DGK-IOTA	Homo sapiens (human)	acquired immunodeficiency syndrome alexia cancer dyslexia eclampsia giant cell glioblastoma glioblastoma high grade glioma human immunodeficiency virus infectious disease melanoma schizophrenia skin melanoma
283420	C-type lectin domain containing 9A	CLEC9A Aliases: CD370 DNGR-1 HEEE9341 UNQ9341	Homo sapiens (human)	acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease herpes simplex human immunodeficiency virus infectious disease influenza leprosy pneumonia primary immunodeficiency disease tuberculosis viral infectious disease
341880	solute carrier family 35 member F4	SLC35F4 Aliases: FLJ37712	Homo sapiens (human)	acquired immunodeficiency syndrome bipolar disorder
11018	transmembrane p24 trafficking protein 1	TMED1 Aliases: IL1RL1LG Il1rl1l MGC1270 ST2L p24g1 p24gamma1	Homo sapiens (human)	acquired immunodeficiency syndrome breast cancer human immunodeficiency virus infectious disease
497190	C-type lectin domain family 18 member B	CLEC18B	Homo sapiens (human)	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
123099	delta 4-desaturase, sphingolipid 2	DEGS2 Aliases: DES2 FADS8 dihydroceramide desaturase 2 sphingolipid delta(4)-desaturase 2	Homo sapiens (human)	acquired immunodeficiency syndrome colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis disease of mental health human immunodeficiency virus infectious disease large intestine cancer neurodegenerative disease obesity psychotic disorder schizophrenia type 2 diabetes mellitus
1727	cytochrome b5 reductase 3	CYB5R3 Aliases: B5R NADH-cytochrome b5 reductase 3	Homo sapiens (human)	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension estrogen-receptor negative breast cancer exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
669	bisphosphoglycerate mutase	BPGM	Homo sapiens (human)	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 familial erythrocytosis 8 normocytic anemia polycythemia vera polycythemia stress polycythemia

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