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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 **6626 - 6650** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
255520	ELMO domain containing 2	ELMOD2	Homo sapiens (human)
390059	olfactory receptor family 51 subfamily M member 1	OR51M1	Homo sapiens (human)
3357	5-hydroxytryptamine receptor 2B	HTR2B	Homo sapiens (human)
135295	serine and arginine rich splicing factor 12	SRSF12	Homo sapiens (human)
3099	hexokinase 2	HK2	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction adult medulloblastoma alcoholic hepatitis alcoholic liver cirrhosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy autosomal recessive distal hereditary motor neuronopathy 1 bile duct adenocarcinoma bile duct cancer bile duct carcinoma bone osteosarcoma brain cancer breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cryptococcosis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma distal arthrogryposis early infantile epileptic encephalopathy embryoma endometrial adenocarcinoma epithelioid sarcoma esophagus squamous cell carcinoma extrahepatic bile duct carcinoma fundus albipunctatus gallbladder cancer gallbladder carcinoma gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance glucose metabolism disease head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intrahepatic cholangiocarcinoma inverted follicular keratosis keratoacanthoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer lateral sclerosis leukemia liver cancer liver carcinoma liver cirrhosis low tension glaucoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphoma maturity-onset diabetes of the young medulloblastoma medullomyoblastoma melanoacanthoma melanotic medulloblastoma microphthalmia middle cerebral artery infarction mixed glioma motor neuron disease multiple myeloma myocardial infarction neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete Opitz-GBBB syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma prediabetes syndrome primary open angle glaucoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis silent myocardial infarction skin disease spindle cell sarcoma squamous cell carcinoma stomach cancer stomach carcinoma thyroid gland anaplastic carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uveal melanoma viral infectious disease
10046	mastermind like domain containing 1	MAMLD1	Homo sapiens (human)
9879	DEAD-box helicase 46	DDX46	Homo sapiens (human)
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
151176	erythroferrone	ERFE	Homo sapiens (human)
81	actinin alpha 4	ACTN4	Homo sapiens (human)
730249	aconitate decarboxylase 1	ACOD1 Aliases: CAD	Homo sapiens (human)	bacterial sepsis central nervous system cancer gliosarcoma hepatitis B high grade glioma lung disease mixed glioma peripheral artery disease viral infectious disease
646424	serine peptidase inhibitor Kazal type 8 (putative)	SPINK8	Homo sapiens (human)
5347	polo like kinase 1	PLK1	Homo sapiens (human)
27315	post-GPI attachment to proteins 2	PGAP2 Aliases: CWH43-N FGF receptor activating protein 1 FRAG1 cell wall biogenesis 43 N-terminal homolog (S. cerevisiae)	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Cogan syndrome Hirschsprung's disease Perlman syndrome Sotos syndrome Unverricht-Lundborg syndrome blepharospasm bone osteosarcoma cancer capillary disease childhood osteosarcoma cleft palate craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy embryoma esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 3 hyperphosphatemia intellectual disability isolated cleft palate learning disability monocular esotropia oligohydramnios osteosarcoma scoliosis sensorineural hearing loss syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy
54187	N-acetylneuraminate synthase	NANS	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 Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder bone cancer bone osteosarcoma breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma communicating hydrocephalus congenital central hypoventilation syndrome congenital nystagmus congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis craniosynostosis depressive disorder diabetes mellitus dissociated nystagmus dysthymic disorder embryoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma essential thrombocythemia generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma hydrocephalus hypertrichosis inflammatory liposarcoma intellectual disability learning disability liposarcoma liver cancer liver cirrhosis major depressive disorder malignant fibrous histiocytoma melancholic depression microcephaly mixed glioma mixed sleep apnea mucopolysaccharidosis IV multiple epiphyseal dysplasia myelodysplastic syndrome myocardial infarction neuroblastoma neurotic disorder obesity obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteomyelitis osteosarcoma parapsoriasis pathologic nystagmus peripheral osteosarcoma phobic disorder pleomorphic adenoma pleomorphic liposarcoma polycystic ovary syndrome premenstrual tension prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole restless legs syndrome rhabdomyosarcoma sarcoma sclerosing liposarcoma silent myocardial infarction skin disease sleep apnea social phobia spindle cell sarcoma spondyloepimetaphyseal dysplasia, Genevieve-type spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 synovial sarcoma tongue cancer tongue squamous cell carcinoma type 2 diabetes mellitus well-differentiated liposarcoma
3985	LIM domain kinase 2	LIMK2	Homo sapiens (human)
1991	elastase, neutrophil expressed	ELANE	Homo sapiens (human)
90488	transmembrane protein 263	TMEM263	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
3428	interferon gamma inducible protein 16	IFI16	Homo sapiens (human)
8396	phosphatidylinositol-5-phosphate 4-kinase type 2 beta	PIP4K2B Aliases: PIP5KIIB PIP5KIIbeta	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer embryoma pancreatic cancer pancreatic carcinoma
1809	dihydropyrimidinase like 3	DPYSL3	Homo sapiens (human)
5714	proteasome 26S subunit, non-ATPase 8	PSMD8	Homo sapiens (human)
8624	proteasome assembly chaperone 1	PSMG1	Homo sapiens (human)
5737	prostaglandin F receptor	PTGFR	Homo sapiens (human)

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