schizophrenia 18

Summary
Synonym
  • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
  • SCZD18
Definition
A schizophrenia that has_material_basis_in a mutation of the SLC1A1 gene on chromosome 9p24.2.
Super Class
monogenic disease schizophrenia
Disease Ontology
DOID:0070093
Mondo Disease Ontology
OMIM
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