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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 **8876 - 8900** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
256710	GLIPR1 like 1	GLIPR1L1 Aliases: MGC26856	Homo sapiens (human)
2737	GLI family zinc finger 3	GLI3	Homo sapiens (human)
2736	GLI family zinc finger 2	GLI2	Homo sapiens (human)
2735	GLI family zinc finger 1	GLI1	Homo sapiens (human)
9815	GIT ArfGAP 2	GIT2	Homo sapiens (human)
28964	GIT ArfGAP 1	GIT1	Homo sapiens (human)
79018	GID complex subunit 4 homolog	GID4	Homo sapiens (human)
84514	GH3 domain containing	GHDC	Homo sapiens (human)
348654	GEN1 Holliday junction 5' flap endonuclease	GEN1	Homo sapiens (human)
29925	GDP-mannose pyrophosphorylase B	GMPPB Aliases: KIAA1851 mannose-1-phosphate guanyltransferase beta	Homo sapiens (human)	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia 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 cardiomyopathy cataract centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B14 muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia 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 oligohydramnios ophthalmoplegia optic atrophy pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
29926	GDP-mannose pyrophosphorylase A	GMPPA	Homo sapiens (human)	Addison's disease Down syndrome Laron syndrome achalasia achondroplasia adrenal cortical hypofunction alacrima, achalasia, and impaired intellectual development syndrome blindness coloboma epilepsy intellectual disability learning disability megaesophagus microcephaly nonepidermolytic palmoplantar keratoderma optic atrophy palmoplantar keratosis sensorineural hearing loss triple-A syndrome visual epilepsy
2762	GDP-mannose 4,6-dehydratase	GMDS Aliases: GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	Homo sapiens (human)	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IIc embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
390637	GDP-D-glucose phosphorylase 1	GDPGP1	Homo sapiens (human)
389400	GDNF family receptor alpha like	GFRAL	Homo sapiens (human)
64096	GDNF family receptor alpha 4	GFRA4 Aliases: persephin receptor	Homo sapiens (human)	Hirschsprung's disease allergic asthma asthma intrinsic asthma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A panic disorder
2676	GDNF family receptor alpha 3	GFRA3	Homo sapiens (human)
2675	GDNF family receptor alpha 2	GFRA2 Aliases: GDNFRB NTNRA RETL2 TRNR2	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Parkinsonism adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
2674	GDNF family receptor alpha 1	GFRA1 Aliases: GDNFR GFR-ALPHA-1 RET1L RETL1 TRNR1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Churg-Strauss syndrome Hirschsprung's disease Kennedy's disease Parkinsonism Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyarteritis nodosa polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma renal agenesis rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
145781	GCOM1, MYZAP-POLR2M combined locus	GCOM1	Homo sapiens (human)
10985	GCN1 activator of EIF2AK4	GCN1	Homo sapiens (human)
2638	GC vitamin D binding protein	GC	Homo sapiens (human)
57459	GATA zinc finger domain containing 2B	GATAD2B	Homo sapiens (human)
54815	GATA zinc finger domain containing 2A	GATAD2A	Homo sapiens (human)
57798	GATA zinc finger domain containing 1	GATAD1	Homo sapiens (human)
2626	GATA binding protein 4	GATA4	Homo sapiens (human)

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