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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 **7901 - 7925** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
85455	dispatched RND transporter family member 2	DISP2	Homo sapiens (human)
85456	tankyrase 1 binding protein 1	TNKS1BP1	Homo sapiens (human)
85459	centrosomal protein 295	CEP295	Homo sapiens (human)
85461	tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1	TANC1	Homo sapiens (human)
85463	zinc finger CCCH-type containing 12C	ZC3H12C	Homo sapiens (human)
85464	slingshot protein phosphatase 2	SSH2	Homo sapiens (human)
85465	selenoprotein I	SELENOI Aliases: KIAA1724 SELI SEPI	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome cancer cleft palate coronary artery disease hepatoblastoma hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 81 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia isolated cleft palate liver cancer microcephaly
85476	G elongation factor mitochondrial 1	GFM1	Homo sapiens (human)
85480	thymic stromal lymphopoietin	TSLP	Homo sapiens (human)
85508	scratch family transcriptional repressor 2	SCRT2	Homo sapiens (human)
87178	polyribonucleotide nucleotidyltransferase 1	PNPT1	Homo sapiens (human)
89766	uromodulin like 1	UMODL1	Homo sapiens (human)
89780	Wnt family member 3A	WNT3A	Homo sapiens (human)
89790	sialic acid binding Ig like lectin 10	SIGLEC10 Aliases: MGC126774 PRO940 SIGLEC-10 SLG2 sialic acid binding Ig-like lectin 10 Ig-like lectin 7 siglec-like gene 2	Homo sapiens (human)	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
89792	galactose-3-O-sulfotransferase 3	GAL3ST3 Aliases: GAL3ST2	Homo sapiens (human)
89795	neuron navigator 3	NAV3	Homo sapiens (human)
89796	neuron navigator 1	NAV1	Homo sapiens (human)
89797	neuron navigator 2	NAV2	Homo sapiens (human)
89801	protein phosphatase 1 regulatory subunit 3F	PPP1R3F	Homo sapiens (human)
89822	potassium two pore domain channel subfamily K member 17	KCNK17	Homo sapiens (human)
89832	CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion	CHRFAM7A	Homo sapiens (human)
89845	ATP binding cassette subfamily C member 10	ABCC10	Homo sapiens (human)
89846	FYVE, RhoGEF and PH domain containing 3	FGD3	Homo sapiens (human)
89853	multivesicular body subunit 12B	MVB12B	Homo sapiens (human)
89858	sialic acid binding Ig like lectin 12	SIGLEC12 Aliases: S2V SLG Siglec-12 Siglec-L1 Siglec-XII	Homo sapiens (human)	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus

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