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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 **6151 - 6175** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
54659	UDP glucuronosyltransferase family 1 member A3	UGT1A3 Aliases: UGT1C	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis allergic asthma asthma beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis cryptococcosis diabetes mellitus differentiated thyroid gland carcinoma embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis gallbladder disease glycogen storage disease II hepatitis D influenza intrinsic asthma islet cell tumor leukopenia liver disease lung adenocarcinoma lung cancer neonatal jaundice neutropenia obesity pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54664	transmembrane protein 106B	TMEM106B	Homo sapiens (human)
54665	round spermatid basic protein 1	RSBN1	Homo sapiens (human)
54674	leucine rich repeat neuronal 3	LRRN3	Homo sapiens (human)
54675	cardiolipin synthase 1	CRLS1 Aliases: CLS1 GCD10 GCD10 homolog (S. cerevisiae) dJ967N21.6	Homo sapiens (human)	Coffin-Lowry syndrome adenosarcoma bilateral breast cancer breast cancer breast ductal carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer colitis combined oxidative phosphorylation deficiency 57 depressive disorder dysthymic disorder gastroenteritis hepatitis C hepatocellular carcinoma ileitis ileocolitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mastitis melancholic depression microglandular adenosis nephroblastoma neurotic disorder obsolete melancholia paroxysmal nocturnal hemoglobinuria schizophrenia vascular dementia
54680	zinc finger HIT-type containing 6	ZNHIT6	Homo sapiens (human)
54681	prolyl 4-hydroxylase, transmembrane	P4HTM	Homo sapiens (human)
54682	MANSC domain containing 1	MANSC1	Homo sapiens (human)
54704	pyruvate dehydrogenase phosphatase catalytic subunit 1	PDP1	Homo sapiens (human)
54708	membrane associated ring-CH-type finger 5	MARCHF5	Homo sapiens (human)
54716	solute carrier family 6 member 20	SLC6A20	Homo sapiens (human)
54726	OTU deubiquitinase 4	OTUD4	Homo sapiens (human)
54732	transmembrane p24 trafficking protein 9	TMED9 Aliases: HSGP25L2G p24a2 p24alpha2	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome adult T-cell leukemia/lymphoma alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 cancer central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy epilepsy frontotemporal dementia generalized anxiety disorder large intestine cancer lateral sclerosis malaria motor neuron disease nervous system disease neurodegenerative disease nonpapillary renal cell carcinoma obsolete T-cell lymphoblastic leukemia/lymphoma optic atrophy 1 optic atrophy papillary renal cell carcinoma phototoxic dermatitis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma status epilepticus tuberculosis visual epilepsy
54742	lymphocyte antigen 6 family member K	LY6K Aliases: CT97 FLJ35226 HSJ001348 cancer/testis antigen 97	Homo sapiens (human)	adult lymphoma bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system lymphoma childhood lymphoma diffuse large B-cell lymphoma duodenal ulcer embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma head and neck squamous cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma obsolete ymphosarcoma sarcomatoid carcinoma seminoma squamous cell carcinoma testicular cancer testis seminoma tongue squamous cell carcinoma urinary bladder cancer
54749	ependymin related 1	EPDR1	Homo sapiens (human)
54756	interleukin 17 receptor D	IL17RD	Homo sapiens (human)
54757	FAM20A golgi associated secretory pathway pseudokinase	FAM20A	Homo sapiens (human)
54758	kelch domain containing 4	KLHDC4	Homo sapiens (human)
54760	proprotein convertase subtilisin/kexin type 4	PCSK4	Homo sapiens (human)
54768	HYDIN axonemal central pair apparatus protein	HYDIN	Homo sapiens (human)
54776	protein phosphatase 1 regulatory subunit 12C	PPP1R12C	Homo sapiens (human)
54777	cilia and flagella associated protein 46	CFAP46	Homo sapiens (human)
54780	NSE4 homolog A, SMC5-SMC6 complex component	NSMCE4A	Homo sapiens (human)
54790	tet methylcytosine dioxygenase 2	TET2	Homo sapiens (human)
54795	transient receptor potential cation channel subfamily M member 4	TRPM4	Homo sapiens (human)

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