MeSH Browser

MeSH Supplementary: nephrin
Unique ID: C113267
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/C113267
Entry Term(s): CNF protein, human; NPHS1 protein, human; Nphs1 protein, mouse; Nphs1 protein, rat; nephrosis 1 homolog, nephrin (human) protein, mouse; nephrosis 1 homolog, nephrin (human) protein, rat; nephrosis 1, congenital, Finnish type (nephrin) protein, human
Previous Indexing: *PROTEINS (1998)
Heading Mapped to: *Membrane Proteins
Frequency: 1133
Note: gene nephrin is mutated in congenital nephrotic syndrome; amino acid sequence in first source; GenBank F19541; RefSeq NM_019459 (mouse), NM_004646 (human), NM_022628 (rat)
Source: Mol Cell 1998 Mar;1(4):575-82
Date of Entry: 1998/07/27
Revision Date: 2006/08/22

nephrin MeSH Supplementary Concept Data 2024