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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 **126 - 150** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
653509	surfactant protein A1	SFTPA1 Aliases: COLEC4 SP-A SP-A1 surfactant, pulmonary-associated protein A1A	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 Hermansky-Pudlak syndrome Pick's disease Reye syndrome T cell deficiency X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amnestic disorder amyloidosis anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolitis obliterans bronchiolitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types cerebral degeneration cerebral infarction cerebrovascular disease chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cryptogenic organizing pneumonia cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential thrombocythemia extrinsic allergic alveolitis familial periodic paralysis gastroesophageal reflux disease granular cell carcinoma heart disease hematologic cancer hydrocephalus hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease interstitial lung disease interstitial nephritis intrinsic asthma keratoconus liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis macrocytic anemia mastitis myelodysplastic syndrome myopathy neurodegenerative disease newborn respiratory distress syndrome obesity obsolete T lymphocyte deficiency obstructive hydrocephalus obstructive lung disease osteomalacia otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis pulmonary alveolar proteinosis pulmonary edema pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory syncytial virus infectious disease retrograde amnesia rickets secondary hypertrophic osteoarthropathy senile degeneration of brain shigellosis sinusitis squamous cell carcinoma staphyloenterotoxemia systolic heart failure tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis viral infectious disease
653489	RANBP2 like and GRIP domain containing 3	RGPD3	Homo sapiens (human)
653423	sperm associated antigen 11A	SPAG11A	Homo sapiens (human)
653308	N-acylsphingosine amidohydrolase 2B	ASAH2B Aliases: ASAH2L bA449O16.3 bA98I6.3	Homo sapiens (human)	breast cancer breast carcinoma
653275	cryptic, EGF-CFC family member 1B	CFC1B	Homo sapiens (human)
653269	POTE ankyrin domain family member I	POTEI	Homo sapiens (human)
653247	proline rich protein BstNI subfamily 2	PRB2	Homo sapiens (human)
648791	protein phosphatase 1 regulatory subunit 3G	PPP1R3G	Homo sapiens (human)	obesity steatotic liver disease
647174	serpin family E member 3	SERPINE3	Homo sapiens (human)
646960	serine protease 56	PRSS56	Homo sapiens (human)
646627	LY6/PLAUR domain containing 8	LYPD8	Homo sapiens (human)
646424	serine peptidase inhibitor Kazal type 8 (putative)	SPINK8	Homo sapiens (human)
646000	solute carrier family 35 member G4	SLC35G4	Homo sapiens (human)
645961	SPATA31 subfamily C member 2	SPATA31C2	Homo sapiens (human)
645836	ubiquitin specific peptidase 17 like family member 3	USP17L3	Homo sapiens (human)
645191	leucine rich repeat and Ig domain containing 3	LINGO3	Homo sapiens (human)
645104	clarin 2	CLRN2	Homo sapiens (human)
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	Homo sapiens (human)	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
644524	NK2 homeobox 4	NKX2-4	Homo sapiens (human)
644168	dorsal root ganglia homeobox	DRGX	Homo sapiens (human)
644150	WAS/WASL interacting protein family member 3	WIPF3	Homo sapiens (human)
644070	GSG1 like 2	GSG1L2	Homo sapiens (human)
644041	chromosome 18 open reading frame 63	C18orf63	Homo sapiens (human)
643988	fibronectin type III domain containing 10	FNDC10	Homo sapiens (human)
643866	cerebellin 3 precursor	CBLN3	Homo sapiens (human)

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