MeSH Browser

MeSH Supplementary: Fxr1h protein, mouse
Unique ID: C496283
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C496283
Entry Term(s): Fxr1 protein, mouse; fragile X mental retardation syndrome related protein 1, mouse; fragile X mental retardation, autosomal homolog 1, mouse
Registry Numbers: 0
Heading Mapped to: *RNA-Binding Proteins
Frequency: 55
Note: plays a role in the development of the fragile X mental retardation syndrome; gene FXR1 shares a high degree of sequence homology with FMR1 and also encodes two KH domains and an RGG domain, conferring RNA-binding capabilities; RefSeq NM_008053
Source: Hum Mol Genet 2004 Jul 1;13(13):1291-302
Indexing Information: Fragile X Syndrome; Fragile X Mental Retardation Protein
Date of Entry: 2005/02/14
Revision Date: 2005/07/29

Fxr1h protein, mouse MeSH Supplementary Concept Data 2025