SHOC2 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human SHOC2 wild-type allele is located in the vicinity of 10q25.2 and is approximately 94 kb in length. This allele, which encodes leucine-rich repeat protein SHOC-2, plays a role in protein-protein interactions that mediate phosphatase activity and Ras-dependent signaling. Mutation of the gene is associated with Noonan-like syndrome with loose anagen hair 1.
**Synonyms:** - KIAA0862 - NSLH1 - RAS-Binding Protein SUR8, C. elegans, Homolog of Gene - SHOC2 Leucine Rich Repeat Scaffold Protein wt Allele - SHOC2 Leucine-Rich Repeat Scaffold Protein Gene - SHOC2, Leucine Rich Repeat Scaffold Protein Gene - SOC2 - SUR8 - Soc-2 (Suppressor of Clear, C. elegans) Homolog Gene - Soc-2 (Suppressor of Clear, C.elegans) Homolog Gene - Soc-2 Suppressor of Clear Homolog (C. elegans) Gene - Soc-2 Suppressor of Clear Homolog Gene - Suppressor of Clear,C. elegans, Homolog of Gene
/api/v1/systems/nci_thesaurus/nodes/C177159Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.