SATB2 protein, human

Preferred Label : SATB2 protein, human;

MeSH note : heterozygous nonsense mutation in gene SATB2 is associated with cleft palate, osteoporosis, and cognitive defects; RefSeq NM_015265.1; NP_056080.1;

MeSH synonym : SATB homeobox 2 protein, human; special AT-rich sequence-binding protein 2, human;

Is substance : O;

Details

Origin ID

C521297;

UMLS CUI

C1958595;

MeSH term(s) associated for indexing
- matrix attachment region binding proteins [MeSH Descriptor]
- transcription factors [MeSH Descriptor]
Record concept(s)
- SATB2 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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