MeSH Browser

MeSH Supplementary: MKS1 protein, human
Unique ID: C509165
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C509165
Entry Term(s): Meckel syndrome, type 1 protein, human
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 24
Note: part of the flagellar apparatus basal body proteome; mutated in Meckel syndrome; RefSeq NM_017777
Source: Nat Genet 2006 Feb;38(2):155-7
Date of Entry: 2006/04/02
Revision Date: 2006/04/19

MKS1 protein, human MeSH Supplementary Concept Data 2025