Gene List: 
AARS, AIFM1, ATL1, ATP7A, BICD2, BSCL2, DCTN1, DNAJB2, DNM2, DNMT1, DYNC1H1, EGR2, ELP1, FGD4, FIG4, GAN, GARS, GDAP1, GJB1, GNB4, HARS, HINT1, HSPB1, HSPB8, IGHMBP2, INF2, KIF1A, KIF5A, LITAF, LMNA, LRSAM1, MED25, MFN2, MORC2, MPZ, MTMR2, NDRG1, NEFL, NGF, NTRK1, PDK3, PLEKHG5, PMP22, PRPS1, PRX, RAB7A, REEP1, RETREG1, SBF1, SBF2, SCN11A, SCN9A, SH3TC2, SLC12A6, SLC52A2, SLC52A3, SLC5A7, SPTLC1, SPTLC2, TFG, TRIM2, TRPV4, TTR, WNK1, YARS

References: 
Auer-Grumbach M. Hereditary sensory and autonomic neuropathies. Handb Clin Neurol. 2013;115:893-906.

Boyer O, et al. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis. J Am Soc Nephrol. 2011 Feb;22(2):239-45.

Rotthier A, et al. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain. 2009 Oct;132(Pt 10):2699-711.