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 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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DYNC1H1
1778
15
11
9
2
15