MID1 wt Allele

Preferred Label : MID1 wt Allele;

NCIt synonyms : Midline 1 (Opitz/BBB Syndrome) Gene; MIDIN; OGS1; FXY; ZNFXY; TRIM18; OSX; XPRF; OS; RNF59; GBBB1; BBBG1; Midline 1 wt Allele; Midline 1 RING Finger Gene; Zinc Finger on X and Y, Mouse, Homolog of Gene; Finger on X and Y, Mouse, Homolog of Gene;

NCIt definition : Human MID1 wild-type allele is located in the vicinity of Xp22.2 and is approximately 388 kb in length. This allele, which encodes E3 ubiquitin-protein ligase Midline-1 protein, plays a role in the modulation of microtubule organization. Mutations in this gene may be associated with the X-linked form of Opitz syndrome.;

GenBank Accession Number : Y13667;

Détails

Origin ID

C75731;

UMLS CUI

C2697964;

OMIM relation
- Midline 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- Xp22.2 [NCIt concept]
gene_is_element_in_pathway
- Ubiquitin-mediated Proteolysis Pathway [NCIt concept]
gene_plays_role_in_process
- Microtubule Process [NCIt concept]
- Monoubiquitination [NCIt concept]
- Ubiquitinated Protein Degradation [NCIt concept]
- Ubiquitination [NCIt concept]

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