acyl-CoA synthetase family member 3

Summary
Gene Symbol
  • ACSF3
Aliases
  • malonyl-CoA synthetase
Organism
Homo sapiens (human)
External Links
NCBI Gene
197322
HGNC
27288
KEGG Gene ID
hsa:197322
PubChem
197322
Alliance of Genome Resources
Annotation
Keyword
  • ATP-binding
  • Fatty acid metabolism
  • Ligase
  • Mitochondrion
  • Proteomics identification
  • Reference proteome
  • Transit peptide
Proteins
Displaying all 2 entries
UniProt Protein Name
F5H5A1
Q4G176
  • Acyl-CoA synthetase family member 3
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
KEGG BRITE Database
Orthology
K18660
Name
malonyl-CoA/methylmalonyl-CoA synthetase [EC:6.2.1.76 6.2.1.-]
References
Disease
Disease Ontology
Displaying entries 11 - 18 of 18 in total
DO ID Disease Name Source
DOID:5823 childhood lymphoma
DOID:5825 adult lymphoma
DOID:6364 migraine
DOID:655 inherited metabolic disorder
DOID:707 B-cell lymphoma
DOID:8675 obsolete ymphosarcoma
DOID:936 brain disease
DOID:9993 hypoglycemia
The Human Phenotype Ontology
Displaying entries 11 - 20 of 25 in total
HPO ID HPO Term
HP:0001943 Hypoglycemia
HP:0001944 Dehydration
HP:0001993 Ketoacidosis
HP:0002013 Vomiting
HP:0002014 Diarrhea
HP:0002076 Migraine
HP:0002254 Intermittent diarrhea
HP:0002354 Memory impairment
HP:0002384 Focal impaired awareness seizure
HP:0002910 Elevated circulating hepatic transaminase concentration
Displaying all 2 entries
Disease ID Disease Name
ORPHA:289504
  • combined malonic and methylmalonic acidemia
OMIM:614265
  • combined malonic and methylmalonic acidemia
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP006785
Gene Name
acyl-CoA synthetase family member 3
Ortholog
Displaying entries 91 - 92 of 92 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
103255185 CARSF27502
115619563 STRHB07294

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Last updated: August 19, 2024