Gene table: search width pubmed_id = 26462740


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

protein
All allelic disease phenotypes - locus/disease symbols
Neuronopathy, distal hereditary motor, autosomal dominant 10 - (AD)
12.33
26462740
EMILIN1 (2p23.3)
Elastin microfibril interfacer 1
* Neuronopathy, distal hereditary motor, autosomal dominant 10 - HMND10