GlyCosmos Portal

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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 **8151 - 8175** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
51493	RNA 2',3'-cyclic phosphate and 5'-OH ligase	RTCB	Homo sapiens (human)
140876	RIPOR family member 3	RIPOR3	Homo sapiens (human)
55781	RIO kinase 2	RIOK2	Homo sapiens (human)
23504	RIMS binding protein 2	RIMBP2	Homo sapiens (human)
9750	RHO family interacting cell polarization regulator 2	RIPOR2	Homo sapiens (human)
79567	RHO family interacting cell polarization regulator 1	RIPOR1	Homo sapiens (human)
91869	RFT1 homolog	RFT1 Aliases: CDG1N congenital disorder of glycosylation 1N	Homo sapiens (human)	Crohn's colitis Crohn's disease Laron syndrome Unverricht-Lundborg syndrome West syndrome achondroplasia blepharospasm blindness blood coagulation disease cancer clubfoot congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis early myoclonic encephalopathy epilepsy focal hand dystonia hypertropia inflammatory bowel disease 1 inflammatory bowel disease mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy obsolete inherited blood coagulation disease ophthalmoplegia schizophrenia sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 type 2 diabetes mellitus ulcerative colitis visual epilepsy
5986	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	RFNG	Homo sapiens (human)
5980	REV3 like, DNA directed polymerase zeta catalytic subunit	REV3L	Homo sapiens (human)
23186	REST corepressor 1	RCOR1	Homo sapiens (human)
768211	RELT like 1	RELL1	Homo sapiens (human)
84957	RELT TNF receptor	RELT	Homo sapiens (human)
5971	RELB proto-oncogene, NF-kB subunit	RELB	Homo sapiens (human)
5970	RELA proto-oncogene, NF-kB subunit	RELA	Homo sapiens (human)
5966	REL proto-oncogene, NF-kB subunit	REL	Homo sapiens (human)
5978	RE1 silencing transcription factor	REST	Homo sapiens (human)
92241	RCSD domain containing 1	RCSD1	Homo sapiens (human)
91433	RCC1 domain containing 1	RCCD1	Homo sapiens (human)
100526737	RBM14-RBM4 readthrough	RBM14-RBM4	Homo sapiens (human)
9821	RB1 inducible coiled-coil 1	RB1CC1	Homo sapiens (human)
5934	RB transcriptional corepressor like 2	RBL2	Homo sapiens (human)
5925	RB transcriptional corepressor 1	RB1	Homo sapiens (human)
5932	RB binding protein 8, endonuclease	RBBP8	Homo sapiens (human)
5930	RB binding protein 6, ubiquitin ligase	RBBP6	Homo sapiens (human)
5928	RB binding protein 4, chromatin remodeling factor	RBBP4	Homo sapiens (human)

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