Synaptosomal-associated protein 29 is a protein that in humans is encoded by the SNAP29 gene. This gene, a member of the SNAP25 gene family, encodes a protein involved...

syndrome is a neurocutaneous condition caused by mutation in the SNAP29 gene. CEDNIK syndrome is a rare congenital condition that presents as severe...

(Genodermatosis) which has been associated with a loss-of-function mutation in SNAP29; SNAP29 is a member of the SNAP Receptor (SNARE) protein family. SNARE proteins...

Proteins in the SNAP-receptor (SNARE protein) family, including: SNAP23 SNAP25 SNAP29 SNAP91, the gene that codes for clathrin coat assembly protein AP180 HT-2157...

Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome (CEDNIK) SNAP29 <1:1,000,000 Cleft palate short stature vertebral anomalies syndrome Combined...

membrane fusion of the constitutive exocytosis, probably, is mediated by SNAP29 and Syntaxin19 at the plasma membrane and YKT6 or VAMP3 at the vesicle membrane...

neuropathy, ichthyosis, keratoderma syndrome 609528 Autosomal recessive SNAP29 Arthrogryposis, renal dysfunction, cholestasis syndrome 208085 Autosomal...

attaches to the membrane. SNAP29, however, is binds to syntaxin on vesicles membranes rather than to plasma membranes. SNAP29 has also been found to be...

identified as an autophagosome associated SNARE that interacts with VAMP8 and SNAP29 and is required for fusion with the lysosome. STX17 is localized on the...

2001). "Association of insulin-like growth factor 1 receptor with EHD1 and SNAP29". The Journal of Biological Chemistry. 276 (35): 33054–60. doi:10.1074/jbc...