STX1B wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human STX1B wild-type allele is located in the vicinity of 16p11.2 and is approximately 21 kb in length. This allele, which encodes syntaxin-1B protein, plays a role in synaptic transmission and vesicle trafficking. Mutations in the gene are associated with generalized epilepsy with febrile seizures plus 9.

**Synonyms:** - GEFSP9 - STX1B1 - STX1B2 - Syntaxin 1B wt Allele - Syntaxin 1B1 Gene - Syntaxin 1B2 Gene