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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 **1726 - 1750** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
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
54872	phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group)	PIGG Aliases: FLJ20265 GPI ethanolamine phosphate transferase 2 GPI7 LAS21 LAS21 (GPI7) homolog (S. cerevisiae)	Homo sapiens (human)	cerebral degeneration epilepsy intellectual disability learning disability placental insufficiency visual epilepsy
54898	ELOVL fatty acid elongase 2	ELOVL2 Aliases: Ssc2	Homo sapiens (human)	acute chest syndrome acute myocardial infarction autism spectrum disorder autistic disorder central nervous system cancer coronary artery disease coronary thrombosis giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma myocardial infarction papillary adenocarcinoma papillary renal cell carcinoma silent myocardial infarction skin melanoma steatotic liver disease thyroid gland papillary carcinoma
54916	transmembrane protein 260	TMEM260	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis T-cell non-Hodgkin lymphoma acute myeloid leukemia alcohol dependence alcohol use disorder cancer double outlet right ventricle embryoma kidney failure lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma stomach cancer ventricular septal defect
54936	ADP-ribosylserine hydrolase	ADPRS Aliases: ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	Homo sapiens (human)	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
54947	lysophosphatidylcholine acyltransferase 2	LPCAT2 Aliases: AGPAT11 FLJ20481 LPLAT9 LysoPAFAT lysophospholipid acyltransferase 9	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer microphthalmia obsolete Matthew-Wood syndrome polycystic ovary syndrome prostate cancer prostate carcinoma
54956	poly(ADP-ribose) polymerase family member 16	PARP16 Aliases: ARTD15 FLJ20509 FLJ25281 pART15	Homo sapiens (human)
54965	phosphatidylinositol glycan anchor biosynthesis class X	PIGX Aliases: FLJ20522 PIG-X	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Laurence-Moon syndrome allergic asthma allergic disease asthma breast cancer breast carcinoma cancer dermatitis embryoma intrinsic asthma polydactyly
54978	solute carrier family 35 member F6	SLC35F6 Aliases: ANT2-binding protein ANT2BP FLJ20555 TANGO9 transport and golgi organization 9 homolog (Drosophila)	Homo sapiens (human)	microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma
54988	acyl-CoA synthetase medium chain family member 5	ACSM5 Aliases: FLJ20581	Homo sapiens (human)
54995	3-oxoacyl-ACP synthase, mitochondrial	OXSM Aliases: CEM1 FASN2D FLJ20604 KS beta-ketoacyl synthase	Homo sapiens (human)	Brucella melitensis brucellosis breast cancer tuberculosis
55032	solute carrier family 35 member A5	SLC35A5 Aliases: FLJ20730	Homo sapiens (human)
55057	crystallin beta-gamma domain containing 2	CRYBG2 Aliases: FLJ38020 beta-gamma crystallin domain containing 2	Homo sapiens (human)
55224	ethanolamine kinase 2	ETNK2 Aliases: EKI2 FLJ10761	Homo sapiens (human)	epilepsy heart conduction disease microcephaly
55247	nei like DNA glycosylase 3	NEIL3 Aliases: FLJ10858 FPG2 ZGRF3 hFPG2 hNEI3 zinc finger, GRF-type containing 3	Homo sapiens (human)	Fanconi anemia acute myocardial infarction basal cell carcinoma cancer coronary thrombosis differentiated thyroid gland carcinoma embryoma giant cell glioblastoma glioblastoma glomerulonephritis hepatocellular carcinoma kidney disease liver cancer myocardial infarction nephritis silent myocardial infarction
55276	phosphoglucomutase 2	PGM2 Aliases: FLJ10983 phosphopentomutase	Homo sapiens (human)
55277	FGGY carbohydrate kinase domain containing	FGGY	Homo sapiens (human)
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B Aliases: FLJ11105 PI4KIIB PIK42B	Homo sapiens (human)	attention deficit hyperactivity disorder bipolar disorder childhood leukemia chronic myeloid leukemia disease of mental health leukemia psychotic disorder schizophrenia
55301	oleoyl-ACP hydrolase	OLAH Aliases: FLJ11106 S-acyl fatty acid synthase thioesterase, medium chain SAST oleoyl-acyl-carrier-protein hydrolase	Homo sapiens (human)	migraine
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 Aliases: FLJ11112 LCB2B hLCB2b	Homo sapiens (human)	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
55326	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5 Aliases: 1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon FLJ11210 LPAAT-e LPAAT-epsilon LPLAT5 lysophosphatidic acid acyltransferase, epsilon lysophospholipid acyltransferase 5	Homo sapiens (human)
55331	alkaline ceramidase 3	ACER3 Aliases: APHC FLJ11238 alkaline phytoceramidase	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia acute myeloid leukemia cerebellar ataxia cerebellar disease cerebral degeneration dystonia hepatocellular carcinoma intellectual disability learning disability leukodystrophy liver cancer melanoma metabolic dysfunction-associated steatohepatitis neurogenic bladder neuropathy peripheral nervous system disease skin melanoma
55343	solute carrier family 35 member C1	SLC35C1 Aliases: FLJ11320 FUCT1 GDP-fucose transporter 1	Homo sapiens (human)	Laron syndrome achondroplasia anxiety disorder cellulitis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc echolalia generalized anxiety disorder hepatocellular carcinoma leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer microcephaly
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 Aliases: FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial	Homo sapiens (human)

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