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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 ▼
20440	beta galactoside alpha 2,6 sialyltransferase 1	St6gal1	Mus musculus (house mouse)	alcohol use disorder high grade glioma
37950	Sialyltransferase	SiaT	Drosophila melanogaster (fruit fly)	alcohol use disorder high grade glioma
27329	angiopoietin like 3	ANGPTL3	Homo sapiens (human)	alcohol use disorder familial hypobetalipoproteinemia 2
30924	angiopoietin-like 3	Angptl3	Mus musculus (house mouse)	alcohol use disorder familial hypobetalipoproteinemia 2
5507	protein phosphatase 1 regulatory subunit 3C	PPP1R3C Aliases: PTG Phosphatase 1, regulatory inhibitor subunit 5 protein targeting to glycogen	Homo sapiens (human)	alcohol use disorder antithrombin III deficiency breast cancer cancer colorectal cancer colorectal carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer hepatocellular carcinoma large intestine cancer liver cancer major depressive disorder melancholic depression neurotic disorder obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency steatotic liver disease thrombophilia type 2 diabetes mellitus
18166	neuropeptide Y receptor Y1	Npy1r	Mus musculus (house mouse)	alcohol use disorder amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
232975	ATPase, Na+/K+ transporting, alpha 3 polypeptide	Atp1a3	Mus musculus (house mouse)	alcohol use disorder alternating hemiplegia of childhood bipolar disorder developmental and epileptic encephalopathy 99 dystonia 12 epilepsy familial hemiplegic migraine nervous system disease
24212	ATPase Na+/K+ transporting subunit alpha 2	Atp1a2	Rattus norvegicus (Norway rat)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
98660	ATPase, Na+/K+ transporting, alpha 2 polypeptide	Atp1a2	Mus musculus (house mouse)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
477	ATPase Na+/K+ transporting subunit alpha 2	ATP1A2	Homo sapiens (human)	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
5471	phosphoribosyl pyrophosphate amidotransferase	PPAT Aliases: GPAT PRAT	Homo sapiens (human)	alcohol dependence alcohol use disorder breast cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatoblastoma hepatocellular carcinoma liver cancer ovarian cancer ovarian carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
130	alcohol dehydrogenase 6 (class V)	ADH6 Aliases: ADH-5	Homo sapiens (human)	alcohol dependence alcohol use disorder anaplastic astrocytoma cancer childhood cerebral astrocytoma embryoma fibrillary astrocytoma gemistocytic astrocytoma hepatocellular carcinoma high grade glioma juvenile pilocytic astrocytoma liver cancer malignant astrocytoma pancreatic cancer pancreatic carcinoma pilocytic astrocytoma protoplasmic astrocytoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma
124	alcohol dehydrogenase 1A (class I), alpha polypeptide	ADH1A	Homo sapiens (human)	alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis anaplastic astrocytoma arteriosclerotic cardiovascular disease atherosclerosis autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia autosomal recessive hypercholesterolemia brain cancer cancer candidiasis childhood cerebral astrocytoma cholestasis coronary artery disease embryoma esophagus squamous cell carcinoma familial hypercholesterolemia fibrillary astrocytoma gallbladder disease gemistocytic astrocytoma hepatitis C hepatocellular carcinoma high grade glioma hypercalcemia hypoparathyroidism immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome juvenile pilocytic astrocytoma liver cancer liver cirrhosis liver disease lung cancer lung non-small cell carcinoma malignant astrocytoma nephrocalcinosis neuroblastoma oral candidiasis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pharynx cancer phosphorus metabolism disease pilocytic astrocytoma protoplasmic astrocytoma pseudohypoparathyroidism steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder
7364	UDP glucuronosyltransferase family 2 member B7	UGT2B7 Aliases: UGT2B9	Homo sapiens (human)	agnosia bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardia cancer cardiovascular system disease clear cell renal cell carcinoma colorectal cancer colorectal carcinoma congestive heart failure diarrhea embryoma endometrial cancer endometrial carcinoma epilepsy gallbladder disease heart disease hepatitis hepatocellular carcinoma kidney cancer large intestine cancer leukopenia liver cancer liver carcinoma liver disease renal carcinoma renal cell carcinoma sarcomatoid carcinoma sickle cell anemia transitional cell carcinoma tuberculosis urinary bladder cancer uterine corpus cancer visual epilepsy
81562	lectin, mannose binding 2 like	LMAN2L Aliases: DKFZp564L2423 VIP36-like VIPL	Homo sapiens (human)	agnosia attention deficit hyperactivity disorder autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52 bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
2762	GDP-mannose 4,6-dehydratase	GMDS Aliases: GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	Homo sapiens (human)	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IIc embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
55500	ethanolamine kinase 1	ETNK1 Aliases: EKI EKI1	Homo sapiens (human)	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease epilepsy heart conduction disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis microcephaly myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma
4166	carbohydrate sulfotransferase 6	CHST6	Homo sapiens (human)	age related macular degeneration amyloidosis corneal dystrophy degeneration of macula and posterior pole granular corneal dystrophy macular corneal dystrophy macular degeneration obsolete asthenopia recurrent corneal erosion
63840	period circadian regulator 2	Per2	Rattus norvegicus (Norway rat)	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
18627	period circadian clock 2	Per2	Mus musculus (house mouse)	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
8864	period circadian regulator 2	PER2	Homo sapiens (human)	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
50799	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	Slc25a13	Mus musculus (house mouse)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
10165	solute carrier family 25 member 13	SLC25A13	Homo sapiens (human)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
10449	acetyl-CoA acyltransferase 2	ACAA2 Aliases: DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
1551	cytochrome P450 family 3 subfamily A member 7	CYP3A7 Aliases: CP37 P450-HFLA	Homo sapiens (human)	adult respiratory distress syndrome allergic asthma asthma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma embryoma endometrial cancer endometrial carcinoma hepatocellular carcinoma intrinsic asthma liver cancer liver cirrhosis lung cancer lung carcinoma newborn respiratory distress syndrome sarcomatoid carcinoma seminoma testicular cancer testicular malignant germ cell cancer testis seminoma uterine corpus cancer

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