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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 **400376 - 400400** of **422592** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
109305771	synaptojanin 1	SYNJ1	Crocodylus porosus (Australian saltwater crocodile)
104306417	synaptojanin 1	SYNJ1	Dryobates pubescens (Downy woodpecker)
100137543	synaptojanin 1	SYNJ1	Papio anubis (olive baboon)
102975496	synaptojanin 1	SYNJ1	Physeter catodon (sperm whale)
100598449	synaptojanin 1	SYNJ1	Nomascus leucogenys (northern white-cheeked gibbon)
112849330	synaptojanin 1	SYNJ1	Puma concolor (puma)
102938143	synaptojanin 1	SYNJ1	Chelonia mydas (Green sea turtle)
122930797	synaptojanin 1	SYNJ1	Bufo gargarizans (Asiatic toad)
107290594	synaptojanin 1	SYNJ1	Protobothrops mucrosquamatus
102752783	synaptojanin 1	SYNJ1	Myotis davidii
131199921	synaptojanin 1	SYNJ1	Ahaetulla prasina
100674046	synaptojanin 1	SYNJ1	Loxodonta africana (African savanna elephant)
103270972	synaptojanin 1	SYNJ1	Carlito syrichta (Philippine tarsier)
128058154	synaptojanin 1	SYNJ1	Budorcas taxicolor (takin)
102890440	synaptojanin 1	SYNJ1	Pteropus alecto (black flying fox)
102518942	synaptojanin 1	SYNJ1	Camelus ferus (Wild Bactrian camel)
121924860	synaptojanin 1	SYNJ1	Sceloporus undulatus (fence lizard)
8867	synaptojanin 1	SYNJ1 Aliases: INPP5G PARK20 inositol polyphosphate-5-phosphatase G phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1	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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease 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 oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
129074166	synaptojanin 1	SYNJ1	Pteronotus mesoamericanus
116833403	synaptojanin 1	SYNJ1	Chelonoidis abingdonii (Abingdon island giant tortoise)
104498225	synaptojanin 1	SYNJ1	Buceros rhinoceros silvestris
116942019	synaptojanin 1	SYNJ1	Petromyzon marinus (sea lamprey)
103767970	synaptojanin 1	SYNJ1	Merops nubicus (carmine bee-eater)
106864120	synaptojanin 1	SYNJ1	Sturnus vulgaris (Common starling)
105820778	synaptojanin 1	SYNJ1	Propithecus coquereli (Coquerel's sifaka)

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