8e22
From Proteopedia
Jump to navigationJump to search
Structural highlights
DiseaseVP37A_HUMAN Autosomal recessive spastic paraplegia type 53. The disease is caused by variants affecting the gene represented in this entry. FunctionVP37A_HUMAN Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in cell growth and differentiation.[1] See AlsoReferences
| ||||||||||||||||||
This page was last modified 07:26, 3 April 2024.