SATB2 wt Allele

Preferred Label : SATB2 wt Allele;

NCIt synonyms : SATB Homeobox 2 wt Allele;

NCIt definition : Human SATB2 wild-type allele is located in the vicinity of 2q33 and is approximately 191 kb in length. This allele, which encodes DNA binding protein SATB2, plays roles in craniofacial development and inhibition of apoptosis. Mutations in this gene are associated with Cleft Palate.;

GenBank Accession Number : AB028956; NM_015265;

Détails

Origin ID

C75581;

UMLS CUI

C2699238;

OMIM relation
- Special at-rich sequence-binding protein 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2q33 [NCIt concept]
gene_plays_role_in_process
- Apoptosis [NCIt concept]
- Cell Differentiation Process [NCIt concept]
- DNA Binding [NCIt concept]
- Developmental Process [NCIt concept]
- Maturation [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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