Name

SPART Gene

spartin

This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]

SEN2 Gene

senescence (cellular)-related 2

SEN3 Gene

senescence (cellular)-related 3

SEN6 Gene

senescence (cellular)-related 6

SEN6A Gene

senescence (cellular)-related 6A

SEN6B Gene

senescence (cellular)-related 6B

SALRNA3 Gene

senescence associated long non-coding RNA 3

SALRNA1 Gene

senescence associated long non-coding RNA 1

SALRNA2 Gene

senescence associated long non-coding RNA 2