Gene table: search width pubmed_id = 26322222


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
Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations - (AR)
2.51
26322222
29855340
TRAPPC11 (4q35.1)
Trafficking protein particle complex 11
* Limb-Girdle, Muscular dystrophy, type 2S - LGMD2S
* Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotype - CMD