MeSH Browser

MeSH Supplementary: SMCR8 protein, mouse
Unique ID: C000618232
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000618232
Entry Term(s): Smith-Magenis syndrome chromosome region candidate 8 protein, mouse
Registry Numbers: 0
Heading Mapped to: *Carrier Proteins
Frequency: 9
Note: a C9orf72-binding partner involved in regulation of mTOR signaling and autophagy
Source: PLoS Genet. 2016 Nov;12(11):e1006443.
Date of Entry: 2017/05/04
Revision Date: 2017/05/04

SMCR8 protein, mouse MeSH Supplementary Concept Data 2025