KEGG   VARIANT: 667v1
Entry
667v1                      Variant                                 
Name
DST mutation
Type
Loss of function
Gene
DST  dystonin [KO:K10382]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 113810
Network
nt06541  Cytoskeleton in neurons
Disease
H00265  Hereditary sensory and autonomic neuropathy
H00584  Epidermolysis bullosa simplex
Reference
  Authors
Manganelli F, Parisi S, Nolano M, Tao F, Paladino S, Pisciotta C, Tozza S, Nesti C, Rebelo AP, Provitera V, Santorelli FM, Shy ME, Russo T, Zuchner S, Santoro L
  Title
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI.
  Journal
Neurology 88:2132-2140 (2017)
DOI:10.1212/WNL.0000000000003992
Reference
  Authors
Groves RW, Liu L, Dopping-Hepenstal PJ, Markus HS, Lovell PA, Ozoemena L, Lai-Cheong JE, Gawler J, Owaribe K, Hashimoto T, Mellerio JE, Mee JB, McGrath JA
  Title
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of  autosomal recessive epidermolysis bullosa simplex.
  Journal
J Invest Dermatol 130:1551-7 (2010)
DOI:10.1038/jid.2010.19
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