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 41 - 50 of 60 in total
DO ID Disease Name Source
DOID:422 congenital structural myopathy
DOID:423 myopathy
DOID:439 neuromuscular junction disease
DOID:440 neuromuscular disease
DOID:4480 achondroplasia
DOID:4766 embryoma
DOID:4905 pancreatic carcinoma
DOID:539 ophthalmoplegia
DOID:540 strabismus
DOID:5517 stomach carcinoma
The Human Phenotype Ontology
Displaying entries 21 - 30 of 60 in total
HPO ID HPO Term
HP:0002355 Difficulty walking
HP:0002359 Frequent falls
HP:0002421 Poor head control
HP:0002460 Distal muscle weakness
HP:0002515 Waddling gait
HP:0002650 Scoliosis
HP:0002747 Respiratory insufficiency due to muscle weakness
HP:0002804 Arthrogryposis multiplex congenita
HP:0002938 Lumbar hyperlordosis
HP:0003198 Myopathy
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

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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