Gene table: search width pubmed_id = 20039086


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
Spastic paraplegia 43, autosomal recessive - (AR)
15.46
20039086
23857908
C19orf12 (19q12)
Chromosome 19 open reading frame 12(M)
* Spastic paraplegia 43, autosomal recessive - SPG43
* Neurodegeneration with brain iron accumulation 4 - NBIA4