Gene table: search width pubmed_id = 15947997


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Dejerine-Sottas hypertrophic neuropathy, dominant - (AD digenic)
14.42
15947997
EGR2 (10q21.1)
Early growth response 2 protein
GJB1 (Xq13.1)
Gap junction protein, beta 1, 32kDa (connexin 32)
* Charcot-Marie-Tooth disease, type 1D - CMT1D
* Charcot-Marie-Tooth neuropathy Type 4E - CMT4E
* Dejerine-Sottas syndrome - DSS
* Neuropathy, congenital hypomyelinating - CHN
* Charcot-Marie-Tooth neuropathy, X-linked - CMTX1