autosomal dominant intellectual developmental disorder 6

Summary
Synonym
  • MRD6
  • autosomal dominant mental retardation 6
  • autosomal dominant non-syndromic intellectual disability 6
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN2B gene on chromosome 12p13.1.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0070036
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2904 GRIN2B glutamate ionotropic receptor NMDA type subunit 2B
Displaying 1 entry
Gene ID Gene Symbol Description Source
14812 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2)
Displaying 1 entry
Gene ID Gene Symbol Description Source
24410 Grin2b glutamate ionotropic receptor NMDA type subunit 2B

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024