MeSH Browser

MeSH Supplementary: VPS13B protein, human
Unique ID: C475722
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C475722
Entry Term(s): COH1 protein, human; Cohen syndrome 1 protein, human; vacuolar protein sorting 13 homolog B (yeast) protein, human
Registry Numbers: 0
Previous Indexing: *MEMBRANE PROTEINS (2003-2007)
Heading Mapped to: *Vesicular Transport Proteins
Frequency: 59
Note: RefSeq NM_184042
Source: Am J Hum Genet 2003 Jun;72(6):1359-69
Date of Entry: 2003/07/21
Revision Date: 2007/05/15

VPS13B protein, human MeSH Supplementary Concept Data 2025