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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 **6776 - 6800** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
348654	GEN1 Holliday junction 5' flap endonuclease	GEN1	Homo sapiens (human)
25929	gem nuclear organelle associated protein 5	GEMIN5	Homo sapiens (human)
50628	gem nuclear organelle associated protein 4	GEMIN4	Homo sapiens (human)
390637	GDP-D-glucose phosphorylase 1	GDPGP1	Homo sapiens (human)
81544	glycerophosphodiester phosphodiesterase domain containing 5	GDPD5 Aliases: GDE2 PP1665	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma neurodegenerative disease rheumatoid arthritis
220032	glycerophosphodiester phosphodiesterase domain containing 4	GDPD4 Aliases: GDE6	Homo sapiens (human)
79153	glycerophosphodiester phosphodiesterase domain containing 3	GDPD3 Aliases: MGC4171	Homo sapiens (human)	Fabry disease Wolman disease chylomicron retention disease lipid storage disease
54857	glycerophosphodiester phosphodiesterase domain containing 2	GDPD2 Aliases: FLJ20207 GDE3 OBDPF osteoblast differentiation promoting factor	Homo sapiens (human)
284161	glycerophosphodiester phosphodiesterase domain containing 1	GDPD1 Aliases: FLJ37451 GDE4	Homo sapiens (human)
2668	glial cell derived neurotrophic factor	GDNF	Homo sapiens (human)
2661	growth differentiation factor 9	GDF9	Homo sapiens (human)
151449	growth differentiation factor 7	GDF7	Homo sapiens (human)
392255	growth differentiation factor 6	GDF6	Homo sapiens (human)
8200	growth differentiation factor 5	GDF5	Homo sapiens (human)
9573	growth differentiation factor 3	GDF3	Homo sapiens (human)
2658	growth differentiation factor 2	GDF2	Homo sapiens (human)
9518	growth differentiation factor 15	GDF15	Homo sapiens (human)
10220	growth differentiation factor 11	GDF11	Homo sapiens (human)
2662	growth differentiation factor 10	GDF10	Homo sapiens (human)
2657	growth differentiation factor 1	GDF1	Homo sapiens (human)
51573	glycerophosphodiester phosphodiesterase 1	GDE1 Aliases: MIR16 membrane interacting protein of RGS16	Homo sapiens (human)
9615	guanine deaminase	GDA Aliases: CYPIN GAH cytoplasmic PSD-95 interactor guanase guanine aminohydrolase nedasin	Homo sapiens (human)
2653	glycine cleavage system protein H	GCSH Aliases: lipoic acid-containing protein	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome amino acid metabolic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II multiple mitochondrial dysfunctions syndrome obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
145781	GCOM1, MYZAP-POLR2M combined locus	GCOM1	Homo sapiens (human)
140687	glucosaminyl (N-acetyl) transferase family member 7	GCNT7 Aliases: dJ1153D9.2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer

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