dicarboxylic aminoaciduria

Summary
Synonym
  • glutamate-aspartate transport defect
Definition
An amino acid metabolic disorder that is characterized by an excess urinary excretion of aspartate and glutamate acidic amino acids.
Super Class
amino acid metabolic disorder autosomal recessive disease
Disease Ontology
DOID:0060650
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6505 SLC1A1 solute carrier family 1 member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
20510 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25550 Slc1a1 solute carrier family 1 member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
188744 glt-4 Amino acid transporter;Putative sodium-dependent excitatory amino acid transporter glt-4

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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: December 9, 2024