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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 **9401 - 9425** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
10423	CDP-diacylglycerol--inositol 3-phosphatidyltransferase	CDIPT Aliases: PIS PIS1 phosphatidylinositol synthase	Homo sapiens (human)	cancer disorder of sexual development hermaphroditism myasthenia gravis pseudohermaphroditism steatotic liver disease
8760	CDP-diacylglycerol synthase 2	CDS2 Aliases: phosphatidate cytidylyltransferase 2	Homo sapiens (human)	cancer congestive heart failure eye disease
1040	CDP-diacylglycerol synthase 1	CDS1 Aliases: phosphatidate cytidylyltransferase	Homo sapiens (human)	B-cell lymphoma appendicitis arachnoiditis bipolar disorder breast cancer cancer carcinoma carotid stenosis chondrosarcoma colorectal cancer colorectal carcinoma congestive heart failure depressive disorder diffuse large B-cell lymphoma embryoma exanthema subitum eye disease giant cell glioblastoma glioblastoma high grade glioma large intestine cancer meningitis milker's nodule myasthenia gravis obsolete ymphosarcoma panic disorder sarcomatoid carcinoma substance abuse substance-related disorder temporal arteritis variola major
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA Aliases: 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Homo sapiens (human)	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia 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 cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
55602	CDKN2A interacting protein	CDKN2AIP	Homo sapiens (human)
25792	CDKN1A interacting zinc finger protein 1	CIZ1	Homo sapiens (human)
55755	CDK5 regulatory subunit associated protein 2	CDK5RAP2	Homo sapiens (human)
54901	CDK5 regulatory subunit associated protein 1 like 1	CDKAL1	Homo sapiens (human)
143384	CDK2 associated cullin domain 1	CACUL1	Homo sapiens (human)
23580	CDC42 effector protein 4	CDC42EP4	Homo sapiens (human)
10602	CDC42 effector protein 3	CDC42EP3	Homo sapiens (human)
11135	CDC42 effector protein 1	CDC42EP1	Homo sapiens (human)
55561	CDC42 binding protein kinase gamma	CDC42BPG	Homo sapiens (human)
9578	CDC42 binding protein kinase beta	CDC42BPB	Homo sapiens (human)
8476	CDC42 binding protein kinase alpha	CDC42BPA	Homo sapiens (human)
1195	CDC like kinase 1	CLK1	Homo sapiens (human)
83692	CD99 molecule like 2	CD99L2	Homo sapiens (human)
4267	CD99 molecule (Xg blood group)	CD99	Homo sapiens (human)
10225	CD96 molecule	CD96	Homo sapiens (human)
22918	CD93 molecule	CD93 Aliases: C1qR(P) C1qRP CDw93 ECSM3 dJ737E23.1	Homo sapiens (human)	Kuhnt-Junius degeneration acute leukemia acute myocardial infarction allergic asthma asthma cancer central nervous system cancer chronic fatigue syndrome coronary artery disease coronary thrombosis embryoma encephalitis encephalomyelitis giant cell glioblastoma glioblastoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung non-small cell carcinoma mixed glioma myelitis myocardial infarction nasopharynx carcinoma parapsoriasis psoriasis pustulosis of palm and sole silent myocardial infarction thyroid gland carcinoma vascular cancer
928	CD9 molecule	CD9	Homo sapiens (human)
942	CD86 molecule	CD86	Homo sapiens (human)
8832	CD84 molecule	CD84	Homo sapiens (human)
9308	CD83 molecule	CD83	Homo sapiens (human)
3732	CD82 molecule	CD82	Homo sapiens (human)

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