nephrin - CISMeF

Preferred Label : nephrin;

MeSH 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);

CISMeF synonym : NPHS1 protein, human; Nphs1 protein, mouse; Nphs1 protein, rat;

MeSH hyponym : nephrosis 1 homolog, nephrin (human) protein, mouse; nephrosis 1 homolog, nephrin (human) protein, rat; nephrosis 1, congenital, Finnish type (nephrin) protein, human; CNF protein, human;

Is substance : O;

Details

Origin ID

C113267;

UMLS CUI

C0754893;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
Record concept(s)
- NPHS1 protein, human [MeSH concept]
- Nphs1 protein, mouse [MeSH concept]
- Nphs1 protein, rat [MeSH concept]
- nephrin [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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