triosephosphate isomerase 1

Summary
Gene Symbol
  • TPI1
Organism
Homo sapiens (human)
External Links
NCBI Gene
7167
HGNC
12009
KEGG Gene ID
hsa:7167
PubChem
7167
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Alternative promoter usage
  • Alternative splicing
  • Cytoplasm
  • Direct protein sequencing
  • Disease variant
  • Gluconeogenesis
  • Glycolysis
  • Hereditary hemolytic anemia
  • Isomerase
  • Isopeptide bond
  • Lyase
  • Methylation
  • Nitration
  • Phosphoprotein
  • Reference proteome
  • Ubl conjugation
Proteins
Displaying all 3 entries
UniProt Protein Name
Q53HE2
V9HWK1
P60174
  • Methylglyoxal synthase
  • Triose-phosphate isomerase
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K01803
Name
triosephosphate isomerase (TIM) [EC:5.3.1.1]
References
Disease
Disease Ontology
Displaying entries 71 - 80 of 167 in total
DO ID Disease Name Source
DOID:162 cancer
DOID:1749 squamous cell carcinoma
DOID:1811 reflex sympathetic dystrophy
DOID:1826 epilepsy
DOID:1909 melanoma
DOID:1936 atherosclerosis
DOID:1949 cholecystitis
DOID:2348 arteriosclerotic cardiovascular disease
DOID:2349 arteriosclerosis
DOID:2373 hereditary elliptocytosis
The Human Phenotype Ontology
Displaying entries 31 - 40 of 42 in total
HPO ID HPO Term
HP:0002878 Respiratory failure
HP:0003198 Myopathy
HP:0003202 Skeletal muscle atrophy
HP:0003323 Progressive muscle weakness
HP:0003623 Neonatal onset
HP:0004870 Chronic hemolytic anemia
HP:0006579 Prolonged neonatal jaundice
HP:0006597 Diaphragmatic paralysis
HP:0007009 Central nervous system degeneration
HP:0009830 Peripheral neuropathy
Displaying all 2 entries
Disease ID Disease Name
ORPHA:868
  • triosephosphate isomerase deficiency
OMIM:615512
  • triosephosphate isomerase deficiency

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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