Gene table: search width pubmed_id = 24207122


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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 6 - (AD)
12.29
24207122
FBXO38 (5q32)
F-box protein 38
* Distal Spinal Muscular Atrophy with Calf Predominance - HMN2D