Known Diseases associated with this Protein: |  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O
| DEFECTS
| DOMINA
| DOMINANT
| MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (MRD13)
| MENTAL RETARDATION, AUTOSOMAL DOMINANT 13, WITH NEURONAL MIGRATION
| SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT 1, AUTOSOMAL DOMINANT (SMALED1)
| SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL
| SPINAL MUSCULAR ATROPHY, LOWER-EXTREMITY PREDOMINANT, 1, AUTOSOMAL
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|  | Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
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57015308
DYHC1_HUMAN RecName: Full=Cytoplasmic dynein 1 heavy chain 1; AltName: Full=Cytoplasmic dynein heavy chain 1; AltName: Full=Dynein heavy chain, cytosolic
15
11
9
2
15