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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

Search results for "carbohydrate binding"

Displaying entries **276 - 300** of **12902** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
140578	chondrolectin	CHODL Aliases: FLJ12627 MT75 PRED12	Homo sapiens (human)	bronchus cancer bronchus carcinoma bulimia nervosa cancer idiopathic scoliosis lung cancer lung carcinoma lung non-small cell carcinoma progressive muscular atrophy spinal muscular atrophy
142683	intelectin 2	ITLN2 Aliases: HL-2	Homo sapiens (human)
143903	layilin	LAYN Aliases: FLJ30977 FLJ31092	Homo sapiens (human)	arthritis arthropathy bronchus cancer bronchus carcinoma cancer chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm colorectal cancer embryoma gastroenteritis gliosarcoma glomerulonephritis high grade glioma ileitis ileocolitis kidney disease large intestine cancer lung cancer lung carcinoma mixed glioma nephritis osteoarthritis
148003	galectin 16	LGALS16	Homo sapiens (human)	congestive heart failure diffuse large B-cell lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma
154790	C-type lectin domain family 2 member L	CLEC2L Aliases: FLJ32986	Homo sapiens (human)
158326	FRAS1 related extracellular matrix 1	FREM1 Aliases: C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	Homo sapiens (human)	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
160364	C-type lectin domain family 12 member A	CLEC12A Aliases: CD371 CLL-1 DCAL-2 MICL dendritic cell-associated lectin 2 myeloid inhibitory C-type lectin-like receptor	Homo sapiens (human)	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
161198	C-type lectin domain containing 14A	CLEC14A	Homo sapiens (human)	IgA glomerulonephritis breast cancer cancer embryoma lung adenocarcinoma lung cancer melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma thymic carcinoma thymoma
170501	polypeptide N-acetylgalactosaminyltransferase 10	Galnt10	Rattus norvegicus (Norway rat)
171212	polypeptide N-acetylgalactosaminyltransferase 10	Galnt10	Mus musculus (house mouse)
175558	Ricin B lectin domain-containing protein;putative N-acetylgalactosaminyltransferase 6	gly-6	Caenorhabditis elegans
176112	Polypeptide N-acetylgalactosaminyltransferase 3	gly-3	Caenorhabditis elegans	heart valve disease
176557	putative N-acetylgalactosaminyltransferase 9	gly-9	Caenorhabditis elegans
176647	Putative polypeptide N-acetylgalactosaminyltransferase 11	gly-11	Caenorhabditis elegans
176736	Polypeptide N-acetylgalactosaminyltransferase 5	gly-5	Caenorhabditis elegans	colorectal cancer
178343	Putative polypeptide N-acetylgalactosaminyltransferase 10;Ricin B lectin domain-containing protein	gly-10	Caenorhabditis elegans
178661	Polypeptide N-acetylgalactosaminyltransferase;Ricin B lectin domain-containing protein;putative N-acetylgalactosaminyltransferase 7	gly-7	Caenorhabditis elegans
179335	ATP-dependent 6-phosphofructokinase 2	pfk-1.2	Caenorhabditis elegans	disease of metabolism glycogen storage disease VII glycogen storage disease
180302	Polypeptide N-acetylgalactosaminyltransferase 4;polypeptide N-acetylgalactosaminyltransferase	gly-4	Caenorhabditis elegans	congenital disorder of glycosylation type II
180583	ATP-dependent 6-phosphofructokinase 1	pfk-1.1	Caenorhabditis elegans	disease of metabolism glycogen storage disease VII glycogen storage disease
192280	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	Rattus norvegicus (Norway rat)	alcohol use disorder
207839	polypeptide N-acetylgalactosaminyltransferase 6	Galnt6	Mus musculus (house mouse)
211286	ceroid-lipofuscinosis, neuronal 5	Cln5	Mus musculus (house mouse)	neuronal ceroid lipofuscinosis 5
212032	hexokinase 3	Hk3	Mus musculus (house mouse)	glucose metabolism disease
212996	polypeptide N-acetylgalactosaminyltransferase 17	Galnt17	Mus musculus (house mouse)

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