Known Diseases associated with this Protein: |  CHARCOT-MARIE-TOOTH DISEASE 2M (CMT2M)
| CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2M
| CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B, WITH NEUTROPENIA
| CHARCOT-MARIE-TOOTH DISEASE, DOMINANT, INTERMEDIATE TYPE, B (CMTDIB)
| LETHAL CONGENITAL CONTRACTURE SYNDROME 5 (1 FAMILY)
| LETHAL CONGENITAL CONTRACTURE SYNDROME 5 (LCCS5)
| MYOPATHY, CENTRONUCLEAR, 1
| MYOPATHY, CENTRONUCLEAR, 1 (CNM1)
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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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DNM2
1785
66
1
44
0
23