Gene table: search width pubmed_id = 14681890


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

protein
All allelic disease phenotypes - locus/disease symbols
Myofibrillar myopathy 2 - (AD)
5.2
14681890
CRYAB (11q22.3-q23.1)
Crystallin, alpha B
* Dilated cardiomyopathy related to alpha-crystallin
* Myofibrillar myopathy, alpha-B crystallin related
* Myopathy, myofibrillar, 2 - MFM2
* Charcot-Marie-Tooth disease, axonal, related to CRYAB - CMT2