C179876Level 6
ANO6 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human ANO6 wild-type allele is located in the vicinity of 12q12 and is approximately 266 kb in length. This allele, which encodes anoctamin-6 protein, is involved in phospholipid scrambling. A splice acceptor site mutation is associated with Scott syndrome.
**Synonyms:** - Anoctamin 6 wt Allele - BDPLT7 - DKFZp313M0720 - SCTS - TMEM16F
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Cross-system equivalences0
No cross-system equivalences mapped for this node.