Gene table: search width pubmed_id = 40830826


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 myopathy 26 - (AD)
3.60
40830826
TUBA4A (2q35)
Tubulin, Alpha-4A
* Amyotrophic lateral sclerosis 22 - ALS22
* Congenital myopathy 26 - CMYO26
Charcot-Marie-Tooth disease, axonal - (AR)
14.105
40830826
TUBA4A (2q35)
Tubulin, Alpha-4A
* Amyotrophic lateral sclerosis 22 - ALS22
* Congenital myopathy 26 - CMYO26