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This section gives an overview of the disease, and where available shows the following:
More information can be found in the help pages.
✖Disease ID: | 961 | |
Name: | Mental retardation, X-linked 88; MRX88 | |
Associated with: | 1 target |
Synonyms |
Non-specific X-linked mental retardation | X-linked non-syndromic intellectual disability |
Database Links |
Disease Ontology:
DOID:0050776 OMIM: 300852 Orphanet: ORPHA777 |
Click on the target name to link to its detailed view page
Where available, information is display on the role of the target in the disease; drugs which target the disease and their therapeutic use and side-effects.
If there is mutation data curated in GtoPdb this is indicated, with a link back to the appropriate section on the target detailed view page
Immuno ligand interactions - If available, a table of immuno-relevant ligands is shown. These ligands have been curated as having an association to the disease and possess interaction data with the target in GtoPdb. The approval status of the ligand is shown, along with curator comments and an indication of whether the target is considered the primary target of the ligand.
More information can be found in the help pages.
✖AT2 receptor | |
Comments: | G21V, R324Q, I337V and I53F single nucleotide polymorphisms have been associated with mental retardation. |
References: | 1-3 |
Mutations: | AT2 receptor is associated with 5 mutation. Click here for details ![]() |
Click ligand name to view ligand summary page
Click the arrow in the final column to expand comments
More information can be found in the help pages.
✖No ligand related data available for Mental retardation, X-linked 88; MRX88
1. Bienvenu T, Poirier K, Van Esch H, Hamel B, Moraine C, Fryns JP, Ropers HH, Beldjord C, Yntema HG, Chelly J. (2003) Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation. J Med Genet, 40 (5): 357-9. [PMID:12746399]
2. Renieri A, Pescucci C, Longo I, Ariani F, Mari F, Meloni I. (2005) Non-syndromic X-linked mental retardation: from a molecular to a clinical point of view. J Cell Physiol, 204 (1): 8-20. [PMID:15690397]
3. Vervoort VS, Beachem MA, Edwards PS, Ladd S, Miller KE, de Mollerat X, Clarkson K, DuPont B, Schwartz CE, Stevenson RE et al.. (2002) AGTR2 mutations in X-linked mental retardation. Science, 296 (5577): 2401-3. [PMID:12089445]
4. Ylisaukko-oja T, Rehnström K, Vanhala R, Tengström C, Lähdetie J, Järvelä I. (2004) Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation. Hum Genet, 114 (2): 211-3. [PMID:14598163]