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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
51279	complement C1r subcomponent like	C1RL	Homo sapiens (human)
715	complement C1r	C1R	Homo sapiens (human)
389941	complement C1q like 3	C1QL3	Homo sapiens (human)
10882	complement C1q like 1	C1QL1	Homo sapiens (human)
708	complement C1q binding protein	C1QBP	Homo sapiens (human)
714	complement C1q C chain	C1QC	Homo sapiens (human)
712	complement C1q A chain	C1QA	Homo sapiens (human)
1441	colony stimulating factor 3 receptor	CSF3R	Homo sapiens (human)
1440	colony stimulating factor 3	CSF3	Homo sapiens (human)
1439	colony stimulating factor 2 receptor subunit beta	CSF2RB	Homo sapiens (human)
1438	colony stimulating factor 2 receptor subunit alpha	CSF2RA	Homo sapiens (human)
1437	colony stimulating factor 2	CSF2	Homo sapiens (human)
1436	colony stimulating factor 1 receptor	CSF1R	Homo sapiens (human)
1435	colony stimulating factor 1	CSF1	Homo sapiens (human)
57393	collectrin, amino acid transport regulator	CLTRN	Homo sapiens (human)
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
10584	collectin subfamily member 10	COLEC10 Aliases: CL-10 CL-L1	Homo sapiens (human)	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
1400	collapsin response mediator protein 1	CRMP1	Homo sapiens (human)
340267	collagen type XXVIII alpha 1 chain	COL28A1	Homo sapiens (human)
85301	collagen type XXVII alpha 1 chain	COL27A1	Homo sapiens (human)
136227	collagen type XXVI alpha 1 chain	COL26A1	Homo sapiens (human)
84570	collagen type XXV alpha 1 chain	COL25A1	Homo sapiens (human)
255631	collagen type XXIV alpha 1 chain	COL24A1	Homo sapiens (human)
91522	collagen type XXIII alpha 1 chain	COL23A1	Homo sapiens (human)

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