C52170Level 8
INSR wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human INSR wild-type allele is located within 19p13.3-p13.2 and is approximately 177 kb in length. This allele, which encodes insulin receptor protein, plays a role in the regulation of glucose uptake. Mutations in either the structural gene or processing steps may lead to insulin resistance.
**Synonyms:** - CD220 - HHF5 - Insulin Receptor wt Allele
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Cross-system equivalences0
No cross-system equivalences mapped for this node.