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 **7876 - 7900** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
85236	H2B clustered histone 12	H2BC12	Homo sapiens (human)
85301	collagen type XXVII alpha 1 chain	COL27A1	Homo sapiens (human)
85320	ATP binding cassette subfamily C member 11	ABCC11	Homo sapiens (human)
85329	galectin 12	LGALS12 Aliases: GRIP1	Homo sapiens (human)	acute promyelocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma large intestine cancer
85352	shisa like 1	SHISAL1	Homo sapiens (human)
85360	synapse defective Rho GTPase homolog 1	SYDE1	Homo sapiens (human)
85365	ALG2 alpha-1,3/1,6-mannosyltransferase	ALG2 Aliases: CDG1I CDGIi FLJ14511 NET38 hALPG2	Homo sapiens (human)	Bell's palsy agnosia blindness breast cancer breast carcinoma cancer cataract clubfoot coloboma congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation congenital myasthenic syndrome 14 congenital myasthenic syndrome congenital nystagmus congenital ptosis developmental coordination disorder dissociated nystagmus embryoma epilepsy facial nerve disease facial paralysis familial periodic paralysis giant cell glioblastoma glioblastoma high grade glioma intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy obsolete infantile epileptic encephalopathy pathologic nystagmus ptosis scoliosis spontaneous ocular nystagmus visual epilepsy
85377	MICAL like 1	MICALL1	Homo sapiens (human)
85378	tubulin gamma complex component 6	TUBGCP6	Homo sapiens (human)
85379	KIAA1671	KIAA1671	Homo sapiens (human)
85395	SLX9 ribosome biogenesis factor	SLX9	Homo sapiens (human)
85397	regulator of G protein signaling 8	RGS8	Homo sapiens (human)
85403	ELL associated factor 1	EAF1	Homo sapiens (human)
85406	DnaJ heat shock protein family (Hsp40) member C14	DNAJC14	Homo sapiens (human)
85413	solute carrier family 22 member 16	SLC22A16	Homo sapiens (human)
85439	stonin 2	STON2	Homo sapiens (human)
85440	dedicator of cytokinesis 7	DOCK7	Homo sapiens (human)
85442	kinase non-catalytic C-lobe domain containing 1	KNDC1	Homo sapiens (human)
85444	leucine rich repeat and coiled-coil centrosomal protein 1	LRRCC1	Homo sapiens (human)
85445	contactin associated protein family member 4	CNTNAP4	Homo sapiens (human)
85446	zinc finger homeobox 2	ZFHX2	Homo sapiens (human)
85450	inositol 1,4,5-trisphosphate receptor interacting protein	ITPRIP	Homo sapiens (human)
85451	unk zinc finger	UNK	Homo sapiens (human)
85452	cilia and flagella associated protein 74	CFAP74	Homo sapiens (human)
85453	TSPY like 5	TSPYL5	Homo sapiens (human)

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