Gene table: search width pubmed_id = 9537424


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Neuropathy, congenital hypomyelinating, 1 - ( AR)
14.34
9537424
EGR2 (10q21.1)
Early growth response 2 protein
* Charcot-Marie-Tooth disease, type 1D - CMT1D
* Charcot-Marie-Tooth neuropathy Type 4E - CMT4E
* Dejerine-Sottas syndrome - DSS
* Neuropathy, congenital hypomyelinating, 1 - CHN1