1bp deletion within exon 1 of Syt7; this results in a frameshift after amino acid residue seven of the wild-type protein.
A 1bp deletion in the first coding exon of Syt7 within codon 8 leads to a frameshift.
Syt7M1/Syt7M1 is an enhancer of increased mortality during development phenotype of Syt1AD4/Syt1N13
Syt7M1/Syt7M1 is an enhancer of abnormal neurophysiology | larval stage phenotype of Syt1AD4/Syt1N13
Syt7M1/Syt7M1 is an enhancer of embryonic/larval neuromuscular junction | larval stage phenotype of Syt1AD4/Syt1N13