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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 **1076 - 1100** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
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)
55361	phosphatidylinositol 4-kinase type 2 alpha	PI4K2A Aliases: DKFZP761G1923 PI4KII PIK42A	Homo sapiens (human)	Hermansky-Pudlak syndrome breast cancer cancer embryoma giant cell glioblastoma glioblastoma
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
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
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
55508	solute carrier family 35 member E3	SLC35E3 Aliases: BLOV1	Homo sapiens (human)	cardiovascular system disease heart disease
55512	sphingomyelin phosphodiesterase 3	SMPD3 Aliases: NSMASE2 neutral sphingomyelinase II	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 Ehlers-Danlos syndrome Guillain-Barre syndrome Kallmann syndrome Laron syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sheehan syndrome Zika fever achondroplasia acute myeloid leukemia acute pericementitis aggressive periodontitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration chronic kidney disease chronic obstructive pulmonary disease coronary artery disease embryoma essential thrombocythemia hepatocellular carcinoma hyperphosphatemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency leprosy leukemia liver cancer lymphoid leukemia microcephaly myelodysplastic syndrome myeloid leukemia nervous system disease osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta panhypopituitarism periodontosis primary pulmonary hypertension pulmonary emphysema pulmonary hypertension schizophrenia thymus gland disease transient cerebral ischemia vertebrobasilar insufficiency
55526	dehydrogenase E1 and transketolase domain containing 1	DHTKD1	Homo sapiens (human)	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
55556	enolase superfamily member 1	ENOSF1 Aliases: FUCD HSRTSBETA L-fuconate dehydratase TYMSAS rTS	Homo sapiens (human)	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
55568	polypeptide N-acetylgalactosaminyltransferase 10	GALNT10 Aliases: GalNAc-T10 polypeptide GalNAc transferase 10	Homo sapiens (human)	hepatitis B hepatocellular carcinoma liver cancer schizophrenia

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