| Gene ID | Entry | Entry Name | Protein Name | Type | Information | 16667 | Q9QWL7 | K1C17_MOUSE | Keratin, type I cytoskeletal 17 (Cytokeratin-17) (CK-17) (Keratin-17) (K17) | DISRUPTION PHENOTYPE | Severe alopecia during the first week postbirth, correlating with hair fragility, alterations in follicular histology, and apoptosis in matrix cells. {ECO:0000269|PubMed:12050118}. |
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