HMX1 protein, human

Preferred Label : HMX1 protein, human;

MeSH note : mutation leads to an oculoauricular syndrome; GenBank AC116612;

MeSH synonym : H6 family homeobox 1 protein, human; NKX5-3 protein, human;

Is substance : O;

Details

Origin ID

C530064;

UMLS CUI

C2355025;

MeSH term(s) associated for indexing
- homeodomain proteins [MeSH Descriptor]
- transcription factors [MeSH Descriptor]
Record concept(s)
- HMX1 protein, human [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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