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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 **6751 - 6775** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
27069	growth hormone inducible transmembrane protein	GHITM	Homo sapiens (human)
84514	GH3 domain containing	GHDC	Homo sapiens (human)
2689	growth hormone 2	GH2	Homo sapiens (human)
91227	gamma-glutamyltransferase light chain 2	GGTLC2	Homo sapiens (human)
92086	gamma-glutamyltransferase light chain 1	GGTLC1	Homo sapiens (human)
2686	gamma-glutamyltransferase 7	GGT7 Aliases: D20S101 dJ18C9.2	Homo sapiens (human)
124975	gamma-glutamyltransferase 6	GGT6 Aliases: FLJ90165	Homo sapiens (human)
2687	gamma-glutamyltransferase 5	GGT5 Aliases: GGT-REL	Homo sapiens (human)	hepatocellular carcinoma liver cancer lung benign neoplasm
2678	gamma-glutamyltransferase 1	GGT1	Homo sapiens (human)	ARC syndrome Aicardi-Goutieres syndrome Alagille syndrome 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Leber hereditary optic neuropathy Pick's disease Potter's syndrome Reye syndrome Werner syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia aflatoxins-related hepatocellular carcinoma alcohol dependence alcohol use disorder alcoholic liver cirrhosis allergic asthma ameloblastoma anthracosilicosis anthracosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asbestosis asthma atherosclerosis atrial fibrillation benign recurrent intrahepatic cholestasis bile duct adenocarcinoma bile duct carcinoma biliary atresia breast apocrine carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia cholangiocarcinoma cholecystitis cholestasis chromophobe renal cell carcinoma chronic kidney disease citrullinemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common wart coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic retinopathy differentiated thyroid gland carcinoma distal arthrogryposis embryoma endometrial cancer endometrial carcinoma epithelioid leiomyosarcoma essential hypertension essential thrombocythemia exfoliation syndrome familial hyperlipidemia gallbladder cancer gallbladder carcinoma gallbladder disease gamma-glutamyl transpeptidase deficiency gelatinous drop-like corneal dystrophy gestational diabetes gestational trophoblastic neoplasm glucose intolerance glycogen storage disease VIII granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileus inflammatory bowel disease inflammatory liposarcoma influenza intellectual disability interstitial lung disease intestinal obstruction intrahepatic cholangiocarcinoma intrahepatic cholestasis intrinsic asthma kidney failure large intestine cancer learning disability leiomyosarcoma leukemia liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma maturity-onset diabetes of the young melanoma mitochondrial metabolism disease mitochondrial myopathy morbid obesity myelodysplastic syndrome myocardial infarction myxoid leiomyosarcoma nasopharynx carcinoma neonatal jaundice nodular prostate non-alcoholic fatty liver nonpapillary renal cell carcinoma nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete ymphosarcoma osteoarthritis osteomalacia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma peptic ulcer disease periodontitis polycystic ovary syndrome prediabetes syndrome primary biliary cholangitis progeria progressive familial intrahepatic cholestasis 1 progressive familial intrahepatic cholestasis progressive supranuclear palsy prostate cancer prostate carcinoma prostatic adenoma renal carcinoma renal cell carcinoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tauopathy testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uremia uterine corpus cancer viral infectious disease well-differentiated liposarcoma
199720	gametogenetin	GGN	Homo sapiens (human)
8836	gamma-glutamyl hydrolase	GGH Aliases: GATD10 conjugase folylpolygammaglutamyl hydrolase	Homo sapiens (human)
2677	gamma-glutamyl carboxylase	GGCX	Homo sapiens (human)
23163	golgi associated, gamma adaptin ear containing, ARF binding protein 3	GGA3	Homo sapiens (human)
23062	golgi associated, gamma adaptin ear containing, ARF binding protein 2	GGA2	Homo sapiens (human)
100507003	golgi associated olfactory signaling regulator	GFY	Homo sapiens (human)
389400	GDNF family receptor alpha like	GFRAL	Homo sapiens (human)
64096	GDNF family receptor alpha 4	GFRA4 Aliases: persephin receptor	Homo sapiens (human)	Hirschsprung's disease allergic asthma asthma intrinsic asthma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A panic disorder
2676	GDNF family receptor alpha 3	GFRA3	Homo sapiens (human)
2675	GDNF family receptor alpha 2	GFRA2 Aliases: GDNFRB NTNRA RETL2 TRNR2	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Parkinsonism adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
2674	GDNF family receptor alpha 1	GFRA1 Aliases: GDNFR GFR-ALPHA-1 RET1L RETL1 TRNR1	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 B-cell lymphoma Churg-Strauss syndrome Hirschsprung's disease Kennedy's disease Parkinsonism Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyarteritis nodosa polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma renal agenesis rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
9945	glutamine-fructose-6-phosphate transaminase 2	GFPT2 Aliases: GFAT2 glutamine: fructose-6-phosphate aminotransferase 2	Homo sapiens (human)	Machado-Joseph disease acute myocardial infarction cancer chronic kidney disease coronary thrombosis diabetes mellitus embryoma hyperglycemia lung cancer lung non-small cell carcinoma myocardial infarction ovarian cancer ovarian carcinoma silent myocardial infarction type 2 diabetes mellitus
2673	glutamine--fructose-6-phosphate transaminase 1	GFPT1 Aliases: GFA GFAT GFAT1	Homo sapiens (human)	Bell's palsy Laron syndrome Machado-Joseph disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome achondroplasia agnosia brain cancer breast cancer breast carcinoma cancer centronuclear myopathy clubfoot congenital myasthenic syndrome 12 congenital myasthenic syndrome 4C congenital myasthenic syndrome congenital ptosis congenital structural myopathy developmental coordination disorder diabetes mellitus diabetic ketoacidosis embryoma facial nerve disease facial paralysis familial hyperlipidemia familial periodic paralysis giant cell glioblastoma glioblastoma glomerulonephritis hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertropia isolated elevated serum creatine phosphokinase levels kidney disease liver cancer mechanical strabismus myopathy nasopharynx carcinoma nephritis nephrosis neuromuscular disease neuromuscular junction disease obesity ophthalmoplegia pancreatic cancer pancreatic carcinoma ptosis pyoureter scoliosis stomach cancer stomach carcinoma strabismus tubular aggregate myopathy 1 type 2 diabetes mellitus
85476	G elongation factor mitochondrial 1	GFM1	Homo sapiens (human)
2671	growth factor, augmenter of liver regeneration	GFER	Homo sapiens (human)
2670	glial fibrillary acidic protein	GFAP	Homo sapiens (human)

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