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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 **8676 - 8700** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
148789	beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2 Aliases: MGC39558	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
148808	major facilitator superfamily domain containing 4A	MFSD4A	Homo sapiens (human)
148811	peptidase M20 domain containing 1	PM20D1	Homo sapiens (human)
149041	ring finger and CCCH-type domains 1	RC3H1	Homo sapiens (human)
149076	zinc finger protein 362	ZNF362	Homo sapiens (human)
149095	DC-STAMP domain containing 1	DCST1	Homo sapiens (human)
149175	mannosidase endo-alpha like	MANEAL Aliases: FLJ31434	Homo sapiens (human)	alternating hemiplegia of childhood autonomic neuropathy central nervous system disease nervous system disease neurodegenerative disease
149233	interleukin 23 receptor	IL23R	Homo sapiens (human)
149466	chromosome 1 open reading frame 210	C1orf210	Homo sapiens (human)
149499	leucine rich repeat containing 71	LRRC71	Homo sapiens (human)
149628	pyrin and HIN domain family member 1	PYHIN1	Homo sapiens (human)
149647	golgi associated RAB2 interactor family member 4	GARIN4	Homo sapiens (human)
149954	BPI fold containing family B member 4	BPIFB4	Homo sapiens (human)
149998	lipase I	LIPI Aliases: CT17 LPDL PLA1C PRED5 cancer/testis antigen 17 mPA-PLA1beta membrane-associated phospholipase A1 beta	Homo sapiens (human)
150082	lebercilin LCA5 like	LCA5L	Homo sapiens (human)
150084	immunoglobulin superfamily member 5	IGSF5	Homo sapiens (human)
150094	salt inducible kinase 1	SIK1	Homo sapiens (human)
150159	solute carrier family 9 member B1	SLC9B1	Homo sapiens (human)
150223	YdjC chitooligosaccharide deacetylase homolog	YDJC	Homo sapiens (human)	bronchus cancer bronchus carcinoma celiac disease hepatitis B inflammatory bowel disease 1 inflammatory bowel disease lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
150297	chromosome 22 open reading frame 42	C22orf42	Homo sapiens (human)
150356	chondroadherin like	CHADL	Homo sapiens (human)
150365	meiotic double-stranded break formation protein 1	MEI1	Homo sapiens (human)
150372	NFAT activating protein with ITAM motif 1	NFAM1	Homo sapiens (human)
150468	cytoskeleton associated protein 2 like	CKAP2L	Homo sapiens (human)
150483	tektin 4	TEKT4	Homo sapiens (human)

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