MeSH Browser

MeSH Supplementary: RAI1 protein, human
Unique ID: C431552
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C431552
Entry Term(s): retinoic acid induced 1 protein, human
Registry Numbers: 0
Previous Indexing: *PROTEINS (2001-2006); *Transcription Factors (2011-2020)
Heading Mapped to: *Trans-Activators
Frequency: 74
Note: a protein bearing an N-terminal stretch of polyglutamine; Rai1 is deleted in Smith-Magenis syndrome patients; RefSeq NM_030665
Source: Gene 2001 May 30;270(1-2):69-76
Indexing Information: Smith-Magenis Syndrome
Date of Entry: 2001/07/27
Revision Date: 2019/12/31

RAI1 protein, human MeSH Supplementary Concept Data 2024