C52483Level 5
EMILIN1 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human EMILIN1 wild-type allele is located within 2p23.3 and is approximately 8 kb in length. This allele, which encodes EMILIN-1 protein, plays a role in the regulation of both blood vessel structure and transforming growth factor beta signaling.
**Synonyms:** - DKFZP586M121 - EMI - EMILIN - EMILIN-1 - Elastin Microfibril Interface Located Gene - Elastin Microfibril Interfacer 1 wt Allele - gp115
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Cross-system equivalences0
No cross-system equivalences mapped for this node.