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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 **8601 - 8625** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
144245	ALG10 alpha-1,2-glucosyltransferase B	ALG10B Aliases: KCR1 dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase potassium channel regulator 1	Homo sapiens (human)	long QT syndrome 2 long QT syndrome nonsyndromic deafness sick sinus syndrome
144347	refilin A	RFLNA	Homo sapiens (human)
144402	copine 8	CPNE8	Homo sapiens (human)
144423	glycosyltransferase 1 domain containing 1	GLT1D1 Aliases: FLJ31978	Homo sapiens (human)	St. Louis encephalitis allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis coronary artery disease intrinsic asthma
144448	tetraspanin 19	TSPAN19	Homo sapiens (human)
144455	E2F transcription factor 7	E2F7	Homo sapiens (human)
144568	alpha-2-macroglobulin like 1	A2ML1	Homo sapiens (human)
144811	laccase domain containing 1	LACC1 Aliases: FAMIN FLJ38725 fatty acid metabolism–immunity nexus	Homo sapiens (human)	Crohn's colitis Crohn's disease anterior uveitis arthritis arthropathy exanthem inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis pericarditis ulcerative colitis
144983	heterogeneous nuclear ribonucleoprotein A1 like 2	HNRNPA1L2	Homo sapiens (human)
145173	beta 3-glucosyltransferase	B3GLCT Aliases: B3GTL B3Glc-T beta-1,3-glucosyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome IGSF1 deficiency syndrome Klippel-Feil syndrome Kuhnt-Junius degeneration Meckel syndrome Peters anomaly Peters plus syndrome Tn polyagglutination syndrome age related macular degeneration anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease blindness cataract cerebral degeneration cleft lip cleft palate coloboma communicating hydrocephalus congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus congenital ptosis cornea plana craniosynostosis cryptorchidism degeneration of macula and posterior pole depressive disorder dissociated nystagmus epilepsy eye disease glaucoma heart septal defect hydrocephalus hydronephrosis hypoplastic left heart syndrome hypospadias hypothyroidism imperforate anus inguinal hernia intellectual disability isolated cleft palate learning disability macrocytic anemia macular degeneration major depressive disorder melancholic depression microcephaly myopia myxedema obsolete melancholia obstructive hydrocephalus omphalocele optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus placental insufficiency polyhydramnios popliteal pterygium syndrome ptosis pulmonary valve stenosis recurrent corneal erosion renal hypoplasia scoliosis senile degeneration of brain sensorineural hearing loss spina bifida occulta spondylolisthesis spontaneous ocular nystagmus syndactyly trichohepatoenteric syndrome 1 trichohepatoenteric syndrome umbilical hernia ventricular septal defect visual epilepsy
145264	serpin family A member 12	SERPINA12	Homo sapiens (human)	alpha 1-antitrypsin deficiency obesity type 2 diabetes mellitus
145270	proline rich membrane anchor 1	PRIMA1	Homo sapiens (human)
145389	solute carrier family 38 member 6	SLC38A6	Homo sapiens (human)
145407	armadillo like helical domain containing 4	ARMH4	Homo sapiens (human)
145447	abhydrolase domain containing 12B	ABHD12B Aliases: BEM46L3	Homo sapiens (human)
145483	FAM161 centrosomal protein B	FAM161B	Homo sapiens (human)
145501	isthmin 2	ISM2	Homo sapiens (human)
145581	leucine rich repeat and fibronectin type III domain containing 5	LRFN5	Homo sapiens (human)
145748	LysM domain containing 4	LYSMD4	Homo sapiens (human)
145781	GCOM1, MYZAP-POLR2M combined locus	GCOM1	Homo sapiens (human)
145957	neuregulin 4	NRG4	Homo sapiens (human)
146057	tau tubulin kinase 2	TTBK2	Homo sapiens (human)
146059	codanin 1	CDAN1	Homo sapiens (human)
146177	von Willebrand factor A domain containing 3A	VWA3A	Homo sapiens (human)
146183	otoancorin	OTOA Aliases: CT108 cancer/testis antigen 108	Homo sapiens (human)	X-linked nonsyndromic deafness alpha 1-antitrypsin deficiency autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness complement component 2 deficiency congenital adrenal hyperplasia cytochrome-c oxidase deficiency disease obsolete autosomal recessive nonsyndromic deafness 105 sensorineural hearing loss von Willebrand's disease 2 von Willebrand's disease

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