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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 **8101 - 8125** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
57482	capping protein inhibiting regulator of actin dynamics	CRACD	Homo sapiens (human)
1380	complement C3d receptor 2	CR2	Homo sapiens (human)
1379	complement C3b/C4b receptor 1 like	CR1L	Homo sapiens (human)
1378	complement C3b/C4b receptor 1 (Knops blood group)	CR1	Homo sapiens (human)
8532	carboxypeptidase Z	CPZ	Homo sapiens (human)
119587	carboxypeptidase X, M14 family member 2	CPXM2	Homo sapiens (human)
56265	carboxypeptidase X, M14 family member 1	CPXM1	Homo sapiens (human)
54504	carboxypeptidase vitellogenic like	CPVL	Homo sapiens (human)
80772	ceramide-1-phosphate transfer protein	CPTP Aliases: MGC10334	Homo sapiens (human)	acute pancreatitis pancreatitis
1376	carnitine palmitoyltransferase 2	CPT2 Aliases: CPTASE	Homo sapiens (human)	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer lipid metabolism disorder liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency muscular disease myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
126129	carnitine palmitoyltransferase 1C	CPT1C Aliases: CATL1 CPT1P CPTIC FLJ23809	Homo sapiens (human)	Henoch-Schoenlein purpura autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer congenital hypothyroidism embryoma giant cell glioblastoma glioblastoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 73 high grade glioma hypersensitivity vasculitis hypoglycemia hypothyroidism immune system disease lung benign neoplasm melanoma multiple myeloma myxedema neuropathy obesity papillary adenocarcinoma papillary renal cell carcinoma paraplegia peripheral nervous system disease polyneuropathy skin melanoma steatotic liver disease thyroid gland papillary carcinoma
1375	carnitine palmitoyltransferase 1B	CPT1B Aliases: CPT1-M M-CPT1 carnitine O-palmitoyltransferase 1B	Homo sapiens (human)	Balo concentric sclerosis Down syndrome Pearson syndrome acute myocardial infarction adrenoleukodystrophy bladder carcinoma cancer central nervous system disease chronic recurrent multifocal osteomyelitis colitis congestive heart failure coronary thrombosis embryoma gastroenteritis hepatitis hepatocellular carcinoma ileitis ileocolitis liver cancer morbid obesity myocardial infarction narcolepsy post-traumatic stress disorder restless legs syndrome silent myocardial infarction steatotic liver disease systemic primary carnitine deficiency disease urinary bladder cancer very long chain acyl-CoA dehydrogenase deficiency
1374	carnitine palmitoyltransferase 1A	CPT1A Aliases: CPT1-L L-CPT1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma metabolic dysfunction-associated steatohepatitis mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
79869	cleavage and polyadenylation specific factor 7	CPSF7	Homo sapiens (human)
11052	cleavage and polyadenylation specific factor 6	CPSF6	Homo sapiens (human)
10898	cleavage and polyadenylation specific factor 4	CPSF4	Homo sapiens (human)
53981	cleavage and polyadenylation specific factor 2	CPSF2	Homo sapiens (human)
1373	carbamoyl-phosphate synthase 1	CPS1	Homo sapiens (human)
10404	carboxypeptidase Q	CPQ	Homo sapiens (human)
1371	coproporphyrinogen oxidase	CPOX	Homo sapiens (human)
130749	carboxypeptidase O	CPO Aliases: metallocarboxypeptidase C metallocarboxypeptidase O	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
151835	copine family member 9	CPNE9	Homo sapiens (human)
144402	copine 8	CPNE8	Homo sapiens (human)
8895	copine 3	CPNE3	Homo sapiens (human)
8904	copine 1	CPNE1	Homo sapiens (human)

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