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 31 - 40 of 60 in total
DO ID Disease Name Source
DOID:2527 nephrosis
DOID:2921 glomerulonephritis
DOID:3068 glioblastoma
DOID:3070 high grade glioma
DOID:3074 giant cell glioblastoma
DOID:3459 breast carcinoma
DOID:3571 liver cancer
DOID:3635 congenital myasthenic syndrome
DOID:4090 agnosia
DOID:4195 hyperglycemia
The Human Phenotype Ontology
Displaying entries 41 - 50 of 60 in total
HPO ID HPO Term
HP:0003473 Fatigable weakness
HP:0003551 Difficulty climbing stairs
HP:0003554 Type 2 muscle fiber atrophy
HP:0003593 Infantile onset
HP:0003621 Juvenile onset
HP:0003623 Neonatal onset
HP:0003680 Nonprogressive
HP:0003691 Scapular winging
HP:0003701 Proximal muscle weakness
HP:0003803 Type 1 muscle fiber predominance
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