glutamine--fructose-6-phosphate transaminase 1

Summary
Gene Symbol
  • GFPT1
Aliases
  • GFA
  • GFAT
  • GFAT1
Organism
Homo sapiens (human)
External Links
NCBI Gene
2673
HGNC
4241
KEGG Gene ID
hsa:2673
PubChem
2673
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Aminotransferase
  • Biological rhythms
  • Congenital myasthenic syndrome
  • Disease variant
  • Glutamine amidotransferase
  • Phosphoprotein
  • Reference proteome
  • Repeat
Proteins
Displaying 1 entry
UniProt Protein Name
Q06210
  • D-fructose-6-phosphate amidotransferase 1
  • Glutamine:fructose-6-phosphate amidotransferase 1
  • Hexosephosphate aminotransferase 1
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K00820
Name
glutamine---fructose-6-phosphate transaminase (isomerizing) [EC:2.6.1.16]
References
Disease
Disease Ontology
Displaying entries 11 - 20 of 60 in total
DO ID Disease Name Source
DOID:0111338 isolated elevated serum creatine phosphokinase levels
DOID:1029 familial periodic paralysis
DOID:10534 stomach cancer
DOID:10952 nephritis
DOID:1168 familial hyperlipidemia
DOID:11836 clubfoot
DOID:12506 Bell's palsy
DOID:1319 brain cancer
DOID:13934 facial paralysis
DOID:1425 pyoureter
The Human Phenotype Ontology
Displaying entries 31 - 40 of 60 in total
HPO ID HPO Term
HP:0003199 Decreased muscle mass
HP:0003200 Ragged-red muscle fibers
HP:0003202 Skeletal muscle atrophy
HP:0003236 Elevated circulating creatine kinase concentration
HP:0003325 Limb-girdle muscle weakness
HP:0003388 Easy fatigability
HP:0003391 Gowers sign
HP:0003394 Muscle spasm
HP:0003403 EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
HP:0003443 Decreased size of nerve terminals
Displaying all 3 entries
Disease ID Disease Name
OMIM:610542
  • congenital myasthenic syndrome 12
OMIM:608931
  • congenital myasthenic syndrome 4C
ORPHA:353327
  • obsolete congenital myasthenic syndromes with glycosylation defect
Ortholog
Displaying entry 81 - 81 of 81 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
115618382 STRHB19566

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024