Known Diseases associated with this Protein: |  MYOPATHY, ACTIN, CONGENITAL, WITH CORES
| MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS
| MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS (MPCETM)
| MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION
| MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (CFTD)
| NEMALINE MYOPATHY 3
| NEMALINE MYOPATHY 3 (NEM3)
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|  | Tips: The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model. Clicking a check box on the left will display or hide the corresponding domain(s). To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic. |
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ACTA1
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16
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