autosomal dominant intellectual developmental disorder 8

Summary
Synonym
  • MRD8
  • autosomal dominant mental retardation 8
  • autosomal dominant non-syndromic intellectual disability 8
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN1 gene on chromosome 9q34.3.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0070038
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2902 GRIN1 glutamate ionotropic receptor NMDA type subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14810 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1)
Displaying 1 entry
Gene ID Gene Symbol Description Source
24408 Grin1 glutamate ionotropic receptor NMDA type subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
40665 Nmdar1 NMDA receptor 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source Organism
397953 grin1.L glutamate ionotropic receptor NMDA type subunit 1 L homeolog Xenopus laevis (African clawed frog)
108699855 grin1.S glutamate ionotropic receptor NMDA type subunit 1 S homeolog Xenopus laevis (African clawed frog)

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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