Entity Details

Primary name FGGY
Entity type gene
Source Source Link

Details

PrimaryID55277
RefseqGeneNG_030039
SymbolFGGY
NameFGGY carbohydrate kinase domain containing
Chromosome1
Location1p32.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsFGGY_HUMAN

GO terms

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GOName
GO:0019150 D-ribulokinase activity
GO:0019321 pentose metabolic process
GO:0046835 carbohydrate phosphorylation
GO:0070050 neuron cellular homeostasis

Diseases

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Disease IDSourceNameDescription
105400 OMIMAmyotrophic lateral sclerosis 1 (ALS1)A neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord, resulting in fatal paralysis. Sensory abnormalities are absent. The pathologic hallmarks of the disease include pallor of the corticospinal tract due to loss of motor neurons, presence of ubiquitin-positive inclusions within surviving motor neurons, and deposition of pathologic aggregates. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of the cases. Disease susceptibility is associated with variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
FGGYNSFL1CBioGRID, IntAct26389662 28514442 details
FGGYEAF1BioGRID, IntAct26186194 28514442 details
FGGYMRPS22BioGRID, IntAct30021884 details
FGGYHNRNPLBioGRID28611215 details