TMEM138 protein, human

Preferred Label : TMEM138 protein, human;

MeSH note : mutation leads to ciliopathy; RefSeq NM_016464;

Is substance : O;

Origin ID

C570597;

UMLS CUI

C3490686;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
Record concept(s)
- TMEM138 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]